Brain and Vitamin D - many studies

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Nervous system disorders now the top cause of illness - March 2024

Surging nervous system disorders now top cause of illness: study

• "...43 % of the global population — experienced a neurological condition in 2021"

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Brain problems reduced in both fetus and adult by Vitamin D – Oct 2022

Vitamin D and the Central Nervous System: Causative and Preventative Mechanisms in Brain Disorders
Nutrients 2022, 14, 4353. https:// doi.org/10.3390/nu14204353
Xiaoying Cui1,2 and Darryl W. Eyles 1,2,[email protected]

1. Queensland Centre for Mental Health Research, The Park Centre for Mental Health, Wacol Q4076, Australia
2. Queensland Brain Institute, University of Queensland, St Lucia Q4076, Australia

Twenty of the last one hundred years of vitamin D research have involved investigations of the brain as a target organ for this hormone. Our group was one of the first to investigate brain outcomes resulting from primarily restricting dietary vitamin D during brain development. With the advent of new molecular and neurochemical techniques in neuroscience, there has been increasing interest in the potential neuroprotective actions of vitamin D in response to a variety of adverse exposures and how this hormone could affect brain development and function. Rather than provide an exhaustive summary of this data and a listing of neurological or psychiatric conditions that vitamin D deficiency has been associated with, here, we provide an update on the actions of this vitamin in the brain and cellular processes vitamin D may be targeting in psychiatry and neurology.
 Download the PDF from Vitamin D Life

Introduction

The vitamin D receptor is part of the nuclear receptor super family containing members such as testosterone, estradiol, cortisol, progesterone, vitamin A derivative all-trans retinoic acid and the thyroid hormones [1]. These factors have important roles in the differentiation of all organs including the brain. It is now 21 years since we first suggested that vitamin D was a "possible" neurosteroid [2]. At that time, all we knew from existing research was that immunohistochemical evidences for the vitamin D receptor (VDR) had been shown in non-neuronal glial cells and that vitamin D may affect neurotrophic factor expression in vitro. There was very little knowledge about how vitamin D could exert its genomic effects in brain cells and a complete absence of any understanding about whether, like other neurosteroids, vitamin D would also have more rapid non-genomic actions. Over the last two decades, research on neurons, non-neuronal brain cells, in both human and animal brains, has confirmed not only does the brain possess the molecular machinery for vitamin D's actions, but also that VDRs are functional, that liganded VDRs directly regulate the expression of target genes and that vitamin D in the form of 1,25-hydroxyvitamin D3, 1,25(OH)2D3 can rapidly alter ion channel function [3]. Moreover, only very recently have new epigenetic mechanisms been revealed as gene regulatory pathways that vitamin D targets to affect gene expression in the developing brain [4,5]. As a result of all this research, vitamin D can now be considered an important steroid in brain development [6]. More recently the neuroprotective functions of vitamin D have been highlighted in models of adult brain disorders. Here we integrate these data and outline the molecules and processes vitamin D appears to target in both developing and mature brains and how such actions shape behaviour and brain function.
We are now aware of the large number of non-skeletal targets for vitamin D. In brain cells, changing vitamin D status alters cytokine regulation and has been shown to affect cell differentiation, neurotrophin expression, intracellular calcium signalling, neurotransmitter release, anti-oxidant activity, anti-inflammatory actions, stress responsivity and the expression of genes/proteins important to neuron physiology [7,8]. The purpose of this short update is not to exhaustively summarise all such associations, but to bring the reader up to speed with recent findings using the very latest techniques in molecular manipulation/quantitation and cell visualisation.
With respect to brain disorders, there is now reliable epidemiology linking embryonic or neonatal vitamin D deficiency with an increased risk of neurodevelopmental disorders, such as schizophrenia [9,10], autism [11-14] and, more recently, attention deficit hyperactivity disorder (ADHD) [15-17]. There are also numerous studies suggesting adult vitamin D deficiency can be correlated with certain neurodegenerative conditions. This clinical epidemiological literature has been reviewed elsewhere [18,19], and we will return to this in the final section of this article. Our purpose here will be to focus on the latest preclinical studies modelling these epidemiological links and to discuss plausible biological mechanisms behind disease-relevant phenotypes.
Although we were pioneers in this area, works from a number of laboratories have firmly established the biological plausibility for how low levels of vitamin D could adversely affect how brains form and how this could lead to subtle changes in brain function and behaviour. Our task now is to discover exactly how low levels of vitamin D impair the function of specific brain cells/circuits leading to adult brain disorders and whether correcting vitamin levels and/or the processes affected by impaired vitamin D signalling can diminish phenotype/symptom severity.

Vitamin D Signalling in the Brain, the Basics and Controversies

Early studies reporting levels of vitamin D metabolite levels in the brain produced widely varied results. This has been to a large extent due to technical difficulties in extraction and quantification methods. The major circulatory form of vitamin D, 25- hydroxyvitamin D3, (25(OH)D3), and its active hormonal form, 1,25-hydroxyvitamin D3, 1,25(OH)2D3, have been reported to be present in brain [20,21]. Whilst the exact concentrations are debatable, they are routinely reported as far lower than blood levels. The later use of LC/MS/MS with isotope dilution provides absolute chemical identification due to its selectivity and greater sensitivity. Using this technology, one group shows 25(OH)D3 to be around (4 ng/g tissue) in rodent brain [22,23]. This group used atmospheric pressure, photoionisation which may avoid ion-suppression artifacts which may have affected earlier methods. Very recently, Fu and colleagues developed a method to measure vitamin D metabolites in the human brain and found 25(OH)D3 was measurable, but levels were far lower than those found in the blood around 0.2-0.3 ng/g tissue [24].
With respect to the VDR, despite immunohistochemical studies confirming its presence in human, chick, rat, mouse and zebrafish brains, [25-30] claims that some of the antibodies used may have been less-than-specific and have invited dispute [31,32]. Now unambiguous evidence has been provided using mass-spectrophotometry to electrophoretically resolve proteins from adult rodent brains to identify five unique VDR peptides with a confidence interval greater than 99% [33]. There is also close anatomical overlap between brain regions in rats and humans, with respect to VDR location [25-27,29,34,35]. Consistent close crossspecies overlap in VDR distribution validates the use of rodents in modelling vitamin D-related brain outcomes.
Immunohistochemistry, mRNA and protein analyses all reveal a gradual expression of the VDR in the developing brain [33,36-38]. In the developing brain, the VDR is concentrated in differentiating fields, such as the ependymal surface of the lateral ventricles [39] (the greatest source of cell division in the brain), consistent with vitamin D actions as a differentiation agent. In particular, VDR expression in the nucleus of dopamine neurons which appear very early in brain development correlates tightly with the ontogeny of these neurons [35]. New genomic technologies have now allowed VDR location and activity to be assessed in animal brains. Using clustered regularly interspaced short palindromic repeats (CRISPR), Liu et al. inserted a Cre-expression sequence driven by the endogenous VDR promotor. When such animals were mated with a tdTomato reporter mouse (Ai14; B6.Cg-Gt(ROSA)26Sor tm14 (CAG-tdTomato)Hze/J), intense tdTomato fluorescence was detected in multiple brain regions, including caudate putamen, amygdala, reticular thalamic nucleus, cortex and less intense tdTomato fluorescence in hippocampus, hypothalamus, paraventricular thalamic nucleus (PVH), dorsal raphe and bed nucleus of the stria termi- nalis (BNST). RNAscope confirmed the presence of VDR RNA in these same tdTomato positive neurons. However, perhaps most importantly, 1,25(OH)2D3 (5 gM) selectively depolarised the tdTomato positive but not negative neurons in the PVH, indicating vitamin D directly regulates neuronal activity, but only in VDR-expressing neurons [40].
Immunohistochemical evidences for the enzymes that convert 25(OH)D3 to the active hormonal form of vitamin D, 1,25(OH)2D3, CYP27B1, and enzymes responsible for its breakdown, CYP24A1, have been provided in the foetal [41] and adult human brain [25,42], suggesting the active hormone can be made or removed locally in human brains. The most thorough investigation of expression of the major vitamin D metabolising enzymes CYP24A1, CYP271B and CYP271A in brain cell types was undertaken by Landel and colleagues [43]. Using primary cultures of neurons, astrocytes, microglia and oligodendrocytes (encompassing all major brain cell types), this group showed a broad distribution across all cell types but at a lower level than the kidney and liver. Strikingly, however, the addition of 1,25(OH)2D3 induced a profound upregulation of CYP24A1 only in astrocytes and microglia, a finding also previously observed [44]. Again, genomic technologies have been employed to study the activity of these enzymes. Hendrix et al. created a transgenic mouse that expresses the luciferase reporter under the control of a full-length human CYP27B1 promoter. The organ distribution of CYP27B1 luciferase activity is similar to endogenous CYP27B1 with highest activity in the kidney, testis, brain, skin and bone [45]. Unfortunately, this useful model apparently has not yet been utilised to study what factors upregulate CYP27B1 brain activity.

Vitamin D and Normal Brain Development

A wealth of experimental evidence exists regarding the plausibility for how altering vitamin D signalling could affect critical events in brain development, such as axonal elongation, neurotransmitter synthesis, neurotrophin production and later brain function. Although there are some comprehensive reviews in this space [46,47], here, we bring this up to date.

Vitamin D and Neurite Growth

The addition of 1,25(OH)2D3 to embryonic hippocampal neurons in culture increases neurite outgrowth possibly via an increased nerve growth factor (NGF) [48,49]. We also now have new unpublished data replicating the neurite-promoting potential of 1,25(OH)2D3 in developing dopamine neurons differentiated from (a) a neuroblastoma cell line and (b) dopamine neurons in explant mesencephalic cultures. This action is in line with most other neurosteroids. Now, we are exploring the molecular mechanisms behind these effects. Others have chosen to lesion peripheral neurons and to show that vitamin D enhances axonal repair, myelination and functional recovery [50,51]. The 1,25(OH)2D3 treatment also restores neurite outgrowth in models where it is impeded. The knockdown of the important neuronal epigenetic regulator, MeCP2, in cortical neurons blunts neurite extension potentially through reducing the activity of NFkB pathways. The 1,25(OH)2D3 restores normal outgrowth in this model [52]. Vitamin D deficiency has also been shown to reduce peripheral nerve fibre density [53], and vitamin D has been considered a potential therapeutic in spinal cord repair [54].

Vitamin D and Neurotrophic Factors

The first evidence that vitamin D had any action on brain cells came from the early studies from Didier Wion's group in glioblastoma cells. Early studies showed that vitamin D promoted the expression of NT-3, NT-4 and nerve growth factor (NGF) [48,49,55-57]. Vitamin D-mediated increases in NGF were shown to be highly relevant to neuronal survival in vitro [48,58-60].
Given its prominent role in dopaminergic neuron differentiation (see below) and survival in earlier studies, there was a strong focus on vitamin D and neurotrophic factors important for dopaminergic neurons, such as glial cell line-derived neurotrophic factor (GDNF) [61,62] and now brain-derived neurotrophic factor (BDNF) [63]. Blocking vitamin D-mediated increase in GDNF synthesis prevents vitamin D's trophic effects on these neurons [64]. We have described the genomic proof that vitamin D regulates the transcription of both receptors for GDNF. The 1,25(OH)2D3 suppresses GDNF family receptor alpha 1 (GFRal), but ligand bound VDR binds to the promoter of the other major receptor for this neurotrophin, the proto-oncogene tyrosine-protein kinase receptor Ret (C-Ret), to upregulate C-Ret expression. Accordingly, the maternal absence of vitamin D decreases C-Ret expression in the developing rat mesencephalon [65].
The effect of vitamin D on neurotrophic factors in the developing brain has been far less explored. One study showed DVD-deficiency in rats reduced NGF and GDNF protein in neonatal brains [66]. Reductions in BDNF and transforming growth factor-p1 (Tgf-p1) in DVD-deficient embryonic mouse brains have also been described [67].
Most recently, there have been numerous studies showing a convincing link between hippocampal BDNF levels and vitamin D status in adult animals. Consistent with findings in development where the absence of vitamin D leads to a BDNF deficit, very recent studies show chronic treatment with 1,25(OH)2D3 induces a profound upregulation in BDNF in rat hippocampus [68]. Others show stress- or drug-induced memory deficits correspond with decreased hippocampal BDNF expression that can be restored via chronic supplementation with high doses of cholecalciferol [69,70]. Another study revealed age- induced memory deficits could be reversed with cholecalciferol supplementation with corresponding increases in hippocampal BDNF and NGF expression [71]. In a model of type 2 diabetes in mice, BDNF and phosphorylation of its downstream effector CREB are reduced in the brain, and cholecalciferol restores these and associated behavioural deficits [72].
In summarising this data, 1,25(OH)2D3 increases, and the developmental dietary absence of vitamin D reduces the expression of these crucial neurotrophic factors in neurons [73] and glia in developing and adult brains. Vitamin D's regulation of neurotrophic factors remains a central feature in brain ontogeny.

Vitamin D Regulates the Development of Dopamine Neurons

Since we first reported the VDR within the human substantia nigra [25], we have gone on to confirm the VDR is prominent in neuromelanin containing Tyrosine Hydroxylase (TH) positive human nigral neurons [35]. Vitamin D deficiency during development leads to a reduction in specification factors crucial for dopamine neurons [74,75], alters dopamine turnover [76] and leads to decreased lateral positioning of dopamine neurons that will form the substantia nigra [75]. Importantly, similar developmental anomalies in dopamine neuron ontogeny created by other adverse developmental exposures are rescued by maternal treatment with 1,25(OH)2D3 [77]. To better understand the molecular processes involved, we have used neuroblast cells in which the VDR has been over-expressed. In such a model, we have shown 1,25(OH)2D3 increases TH mRNA [78], drives cells down a dopaminergic lineage [79] and directly targets the promoter of Catechol-o-methyl transferase (COMT), an important enzyme in brain dopamine turnover [79].
One very recent study has examined microRNAs in developing dopamine neurons as epigenetic factors in neuronal maturation. This study showed that in flow cytometry-sorted E14 dopamine neurons from DVD-deficient rat embryos, the expression of a number of microRNAs was increased and that gene-ontology analysis indicated these microRNAs were involved in neuronal differentiation. These authors then examined the functional consequences of this in developing dopamine neurons and showed that some of these microRNAs decreased neurite outgrowth [4]. This represents the first evidence in the brain indicating how vitamin D may epigenetically differentiate dopamine neurons.
Taken together, the decreased expression of dopamine-promoting neurotrophic and specification agents and delayed dopamine neuron maturation in DVD-deficient embryonic brains along with the abundant in vitro evidences for 1,25(OH)2D3 as a maturation agent for dopamine neurons, all confirm a central role for vitamin D in dopamine ontogeny. Given the links between DVD-deficiency and schizophrenia [9,10] and that dopamine abnormalities are perhaps causal in this disease, further studies examining this possible mechanistic link are needed.

Developmental Vitamin D Deficiency Effect on Brain Function and Behaviour

The long-term effects of DVD-deficiency on offspring behaviour have also been extensively studied in both rats and mice. Outcomes vary based on the species used/strain and duration and degree of vitamin D deficiency. Notably, there are alterations in critical early dam/pup interactions, such as maternal licking and grooming [80] and pup ultrasonic vocalisations [5,80], along with signs of delayed motor development [5]. As juveniles or adults, offspring have social behavioural deficits and alterations in stereotyped behavioural phenotypes of relevance to autism [5,80]. Interestingly, vitamin D deficiency leads to subtle increases in testosterone levels in maternal blood [81], a finding which has long-been considered a risk-modifying factor in autism [82]. Additionally, foetal male brains from vitamin D deficient dams have increased testosterone compared to control males. This study went on to show silencing of the major enzyme involved in testosterone breakdown, aromatase, by hypermethylation of its promoter in the brain may be the mechanism [81].
DVD-deficiency also leads to long-term changes in adult behaviours. Novelty [83], or exposure to psychomimetics, such as the N-methyl-D-aspartic acid receptor (NMDA-R) antagonist, MK-801 [84-86] or amphetamine [87], all increase locomotor activity in the adult offspring of DVD-deficient dams. Along with sensitivity to these exposures/agents that release dopamine, DVD-deficient rats have a greater response to antipsychotics that block dopamine 2 receptors [84,88]. Brain functional measures are also abnormal in these animals. Long-term potentiation, a cellular correlate of learning and memory and latent inhibition, a measure of attentional processing are also abnormal in DVD-deficient adults [89,90]. With respect to cognition, DVD-deficient offspring have impaired response inhibition, a deficit normalised by the antipsychotic clozapine [91]. Associative learning is also impaired in DVD-deficient adults [92].
Only recently have investigators begun to assess the impact of vitamin D treatment in dams exposed to either DVD-deficiency or another developmental animal model that induces brain changes, maternal immune activation. Such interventions reverse behavioural phenotypes produced by these models related to anxiety, depression cognition, stereotyped and social behaviours [93,94].
As discussed previously, given the stark differences in the effects of DVD-deficiency on brain development between rats and mice, it is not surprising that the behavioural phenotypes in adult offspring also vary widely [95]. For instance, although there are some similarities in novelty-induced hyperlocomotion [84] and perseverative responses [96], outcomes vary widely in tests of exploratory behaviour [88,97] and locomotor response to psychomimetics [98].
Whether DVD-deficiency affects cognitive performance in children is not clear. Two studies show DVD-deficient children have delayed cognitive development [99,100]. However, these findings were not replicated in much larger studies [15]. A recent meta-analysis that summarised 31 studies could find no conclusive evidence for the association between maternal or child vitamin D status and behavioural or cognitive outcomes in children and adolescents. A summary of twelve mother-child studies (n = 17,136) and five studies just in children (n = 1091) showed low maternal or child 25(OH)D3 levels led to impaired behavioural outcomes in children. In contrast, fifteen mother-child studies (n = 20,778) and eight studies in children (n = 7496) showed no association [101]. A large Finnish nested case-control study (1607 children with learning difficulties with matched controls) also showed no link between maternal 25(OH)D3 levels and behaviour [102].
One small randomised clinical trial (55 infants) in healthy term infants showed a low dose of vitamin D supplementation might benefit gross motor function compared to a higher dose of vitamin D supplementation, but this study lacked a placebo control [103]. There is also a not-insubstantial number of studies that link maternal or childhood vitamin D deficiency to neurodevelopmental psychiatric disorders such as autism, ADHD or schizophrenia [9-11,13,14,100,104,105]. This association is not universally replicated [106,107]; however, the mean population 25(OH)D3 levels in these later studies were much higher, making the association difficult to test. Randomised controlled trials of cholecalciferol supplementation in children with ASD or ADHD show diverse outcomes, some showed no beneficial effects and others reported some symptom relief [108-114]. In the future, trials examining vitamin D levels in mothers/children prior to supplementation are required as supplementing vitamin D-sufficient mothers or children is likely to have minimal effect, as shown in other clinical trials with vitamin D [115].

Vitamin D Is Neuroprotective in Neurons and Adult Brain

There are now sufficient epidemiological studies also linking low levels of 25OHD3 with various neurodegenerative conditions such as Alzheimer's disease, Parkinson's disease and multiple sclerosis. Though many such studies suffer from reverse causality (i.e., low levels of vitamin D are a consequence of disease-induced behavioural changes rather than causal), there has been sufficient interest to launch numerous clinical supplementation trials [116-118]. There have also been studies linking exposure to various toxins with low 25OHD3 levels. Such links have stimulated researchers to initiate mechanistic studies in neuronal cell systems and animal models. Along with the wealth of studies showing vitamin D is neuroprotective via neurotrophin production, here, we have chosen not to focus on the clinical epidemiology, but rather on vitamin D's regulatory actions on calcium in the brain and its neuroprotective actions against reactive oxygen species (ROS) and inflammation as well as its actions in mitigating stress as plausible prophylactic/therapeutic mechanisms. We summarised the potential mechanisms underlying the action of vitamin D (Figure 1). Much of this work is very recent.

Figure 1. Neuroprotective actions of vitamin D in brain.

Calcium-related mechanisms (in blue). Non-genomic actions. The 1,25(OH)2D3 acutely facilitates calcium, influx via L-VGCC. The 1,25(OH)2D3; can also directly bind to TRPV1 to induce calcium influx. Both actions facilitate neuronal function. Genomic actions. Chronic vitamin D treatment decreases Cavl (a L-VGCC subunit) expression which will reduce calcium influx in response to ROS/inflammation or stress.
ROS/inflammation-related mechanisms (in purple). ROS enhances NF-kB nuclear translocation to promote proinflammatory cytokine production. The 1,25(OH)2D3 acts to inhibit this nuclear translocation. By also inhibiting NF-kB expression, 1,25(OH)2D3 reduces iNOS expression and thus, reduces NO production. Finally, 1,25(OH)2D3 increases Nrf2 to enhance the expression of anti-oxidant enzymes including GP, CAT, SOD and HO-1, thus countering ROS toxicity. The 1,25(OH)2D3 also directly facilitates Nrf2 nuclear translocation.
Stress-related mechanisms (in green). Stress increases corticosterone synthesis. In the brain, corticosterone increases inflammatory cytokine production via its receptor (GR). The 1,25(OH)2D3 is neuroprotective by antagonising GR expression.
Neurotrophin-related mechanisms (in yellow). A variety of neurotrophic factors have been shown to counter the effects of stress- or toxin-induced neuronal damage. Historically, 1,25(OH)2D3 has been shown to increase NGF, GDNF, BDNF, NT-3 and NT-4 under such conditions.

Calcium Regulation

Calcium transients are required for normal neuronal function, but if calcium is unbuffered, it is toxic to brain cells. For more than 30 years, we have known how vitamin D regulates calcium uptake in bone cells [119,120] and similar mechanisms appear to act in neurons and the brain. In cultured neurons, 1,25(OH)2D3 retards calcium influx via the downregulation of L-type voltage-sensitive calcium channels, thus potentially preventing toxic outcomes [59,121-123]. In contrast, the rapid non-genomic actions of vitamin D produce the opposite effect, increasing calcium influx in cortical slices, a process that is again dependent on L-type calcium channels [124]. In a seminal study, the non-genomic rapid actions of 1,25(OH)2D3 were investigated in cortical neurons using calcium imaging, electrophysiology and molecular biological techniques. This study confirmed that physiological concentrations of 1,25(OH)2D3 lead to rapid calcium influx, but only in some neurons. Somatic nucleated patch recordings revealed a rapid, 1,25(OH)2D3-evoked increase in high-voltage-activated calcium currents mediated by L-type voltage-gated calcium channels [125]. Whether any of these actions are caused by the putative membrane VDR, Protein disulfide-isomerase A3 (PDIA3), in the brain remains unknown. Genetic variants in L-type voltage-gated calcium channels continue to be implicated in schizophrenia [126]. Given the epidemiological links between DVD-deficiency and schizophrenia [9,10], continued studies in this area are warranted.
Recent research also discovered that 25OHD3 and 1,25(OH)2D3 directly bind to the transient receptor potential vanilloid subfamily member 1 (TRPV1) channel [127]. Binding to the same region as the TRPV1 agonist capsaicin, 25OHD3 can weakly activate TRPV1 and inhibit capsaicin-induced TRPV1 activity. TRVP1 activity modulates immune cell activation and cytokine production through regulating intracellular calcium to mediate nociceptive signals. This, therefore, may be one mechanism for how vitamin D may modulate nociceptive pain pathways, as vitamin D deficiency has been linked to chronic pain [128], although oxidative mechanisms have also been proposed [129].

ROS and Inflammation

Vitamin D increases anti-oxidants, such as glutathione and cytochrome c, to mediate anti-oxidant actions in cultured neurons [121,130] and the brain [131,132]. Along with extracellular calcium, vitamin D deficiency in the adult brain increases ROS along with producing impairments in gamma-aminobutyric acid (GABA) and glutamate release. Importantly, reintroducing dietary vitamin D normalises all deficits [133].
In the brain, microglia are the immunologically responsive cells responsible for the production of inflammatory regulators such as nitric oxide (NO). Early studies showed 1,25(OH)2D3 blocks inducible nitric oxide synthetase in the rat brain in response to autoimmune or inflammatory factors [134-136]. Later studies suggested that oxidative stress may upregulate CYP27B1 in microglia to induce 1,25(OH)2D3 production locally at the site of NO or ROS production to mediate vitamin D's anti-oxidant effects in the brain [133,137,138].
In primary cultured neurons, hypoxia induces apoptotic cell death and interferes with normal calcium signalling. One study, that chose to use cholecalciferol rather than calcitriol, showed that when added to cultured primary neurons exposed to hypoxia, cholecalciferol (10 nM) was anti-apoptotic and preserved calcium signalling though this effect was reversed at high doses. Upregulation of hypoxia-induced factor (HIF)-1a and/or BDNF were considered as the possible protective mechanisms [139], though conversion to calcitriol was not assessed.
DVD-deficiency would also appear to render the foetal environment more prone to oxidative stress. Ali and colleagues reported that DVD-deficient rat placenta produces more of the inflammatory cytokines IL-6 and 1L-113 upon challenge with a viral inflammatory agent [140]. Separately, when microglia were cultured from DVD-deficient mouse brains, they were increased in number, were hyperproliferative and had increased ROS production. Culturing these cells in the presence of calcitriol reversed these changes [141].
In recent years, there appears to have been intense interest in vitamin D's protective actions against ROS and inflammation in the brain induced by numerous disease models. For instance, in hypothyroid juvenile rats, cholecalciferol supplementation (100 or 500 IU/kg/day) prevented hypothyroidism-induced cognitive and learning memory impairments [142]. Plausible mechanisms included elevations in the anti-oxidant enzyme superoxide dismutase (SOD) and thiol content in hippocampus and cortical tissue and reductions in malondialdehyde (MDA), a marker of oxidative stress. Similar restorative outcomes on cognition have been achieved in models of acute inflammation and again these same anti-oxidant processes in the brain were invoked by vitamin D supplementation [143].
In spontaneously hypertensive (SH) rats, infusion of 1,25(OH)2D3 into the hypothalamic paraventricular nucleus (PVN), a brain region maintaining baroreflex and autonomic function, prevented the elevation of ROS stress-related proteins such as NOX2, NOX4 and p22phox. Chronic calcitriol infusion also attenuated microglial activation and reduced tumour necrosis factor (TNF)-a, IL-1 p and IL-6 inflammatory cytokine production. Likely, mechanisms involved the inhibition of the high-mobility group box-1(HMGB1)-receptor for advanced glycation end products (RAGE)/Toll-like receptor (TLR4) and NF-kB in the PVN of SH rats [144].
The effect of vitamin D on NO is also detected in a rat model of cerebral ischemia reperfusion model. Seven days of calcitriol administration prior to ischemic surgery reduced stroke-induced elevation of MDA and NO and increased total anti-oxidant capacity. These effects could be attributed to vitamin D-increasing nuclear factor erythroid 2-related factor 2(Nrf2), a transcription factor that decreases oxidative stress following stroke and/or heme oxygenase (HO-1), a major cytoprotective enzyme with anti-oxidative, and antiinflammatory properties [145,146].
In a traumatic brain injury model, calcitriol treatment reduced MDA production and promoted autophagic flux and activated Nrf2 pathways. Autophagy reduces oxidative stress by a timely removal of damaged substances [147]. Nrf2 is a redox-sensitive transcription factor that binds to anti-oxidant response elements to promote the expression of enzymes/proteins for detoxication and anti-oxidation [148]. Confirmation that these two processes were central to calcitriols protective actions in traumatic brain injury was shown by inhibiting the autophagy using chloroquine or deleting Nrf2 as either action blocked calcitriol's protective effects [149].
In a model of lead-induced neurotoxicity and oxidative stress, decreases in antioxidant molecules GSH, SOD and catalase and increased ROS production are observed in rat cortex. Cholecalciferol reversed these changes possibly via Nrf2 and/or NF-kB mechanism [150]. In a model of experimentally induced epilepsy in young male rats, cholecalciferol not only reduced seizure severity, but corrected associated memory deficits, reduced extracellular calcium, restored anti-oxidative enzymes SOD and glutathione- related enzymes and reduced inflammatory cytokine production in the hippocampus [151].
One neurological disorder commonly associated with ROS-mediated brain damage is Parkinsons's disease (PD). The motor deficits produced by PD are believed to be caused by dopamine neurons dying selectively in the substantia nigra and the associated reduced dopamine release in the dorsal striatum. This is modelled in animals via the intracranial delivery of relatively selective dopaminergic terminal toxins, such as 6-hydroxy dopamine (6-OHDA), or nigral toxins such as 1-methyl-4-phenyltetrahydropyrine (MPTP). In a 6- OHDA-treated mouse, cholecalciferol treatment two weeks after surgical lesion attenuated 6-OHDA-induced increases in the microglia marker CD11b, IL-1p and the oxidative stress marker p47phox, a primary modulator of NADPH oxidase activity and restored some motor functional deficits [152]. Another 6-OHDA study showed that cholecalciferol prevented characteristic losses in dopamine synthetic enzymes and transporters, preserved motor function as well as reduced lipid peroxidation [153]. Another study using MPTP showed coadministration with calcitriol improved motor deficits, reduced dopamine neuron toxicity and reduced ROS production [154]. The mechanism proposed was via an interaction between the liganded VDR and poly(ADP-ribose) polymerase-1(PARP1) to reduce its contribution to ROS-induced cell death. PARP1 pathways have been proposed as one mechanism for dopamine cell death in PD.
ROS production is also linked with other degenerative processes such as Alzheimer's disease. Animal models for Alzheimer's disease frequently employ genetic models that over-express the Tau or amyloid (Ap) proteins that are closely linked with disease pathology. In an amyloid presenilin model, 13 weeks of vitamin D deficiency exacerbated the ROS production in this model by downregulating superoxide dismutase 1 (SOD1), glutathione peroxidase 4 and enhanced the expression of IL-1p, IL-6 and TNFa, along with increased Ap production and Tau phosphorylation [155].
In another amyloid model where rats are injected with Ap1-40, cholecalciferol supplementation reduced Ap -induced MDA levels, increased SOD activity and improved hippocampal neuronal survival [156]. Prolonged vitamin D hypovitaminosis in mice (from 6-weeks-old to 6-months-old) altered the expression of genes involved in amyloid precursor protein homeostasis (Snca, Nep, Psmb5), oxidative stress (Park7), inflammation (Casp4), lipid metabolism (Abca1), signal transduction (Gnb5) and neurogenesis (Plat) [157]. In another distinct amyloid protein mutant mouse model (3xtg-AD), vitamin D levels are dramatically reduced at 9 and 12 months of age. Vitamin D supplementation in this model improves memory possibly via the suppression of collapsin response mediator protein-2 (CRMP2) phosphorylation [158]. An in vitro study has also shown 1,25(OH)2D3 alleviates Tau hyperphosphorylation and reduces ROS in a neuronal cell model treated with Ap possibly via vitamin D's role in enhancing GDNF [159].
Experimentally induced autoimmune encephalitis (EAE) is a mouse model mimicking the autoimmune reaction to myelin proteins inducing multiple sclerosis-like pathology. In this model, calcitriol administration decreased the severity of EAE by attenuating inflammation and demyelination at the spinal cord [160]. This same study also showed calcitriol treatment reduces lymphocyte, macrophage and activated microglia infiltration into the brain. EAE mice have increased blood brain barrier permeability thought to be due at least in part to a reduction in endothelial tight-junction proteins such as ZO-1. This same study showed calcitriol increases this proteins expression. Calcitriol also reduced EAE-induced lipid hydroxylation and enhanced the anti-oxidant enzymes glutathione peroxidase, catalase and SOD.
The 1,25(OH)2D3 not only suppresses inflammation in models of demyelination, but also enhances the differentiation or survival of oligodendrocyte progenitor cells in the spinal cord of a MOG35-55-induced EAE mouse model [161]. The promotion of oligodendrocyte maturation by 1,25(OH)2D3 is also observed in a cuprizone-induced EAE mouse model [162]. Krabbe disease is an inherited leukodystrophy. This demyelinating condition is caused by a galactocerebrosidase (GALC) deficit that results in loss of oligodendrocytes and demyelination. In an animal model of this disorder (GALCtwl/twl; twitcher mouse), supplementing the heterozygous GALC+/ — dam from birth to weaning with cholecalciferol delayed onset of disease-induced locomotor deficits and tremors and extend the life span of offspring [163].

Glucocorticoids and Stress

Glucocorticoid release is the classic endocrine response to stress, and protracted exposure induces neuronal shrinkage then cell death [164]. The effects of 1,25(OH)2D3 and glucocorticoids in the body can be considered antagonistic [165-169]. Similarly, in the brain, 1,25(OH)2D3 antagonises the effects of dexamethasone (a corticosterone agonist) on hippocampal neuron differentiation and glucocorticoid receptor function [170]. Interestingly, dexamethasone can decrease 1,25(OH)2D3 synthesis in the hippocampus and prefrontal cortex, indicating this process is reversible [171].
Behaviourally, vitamin D antagonises the depression-like phenotypes induced by chronic cortisol administration in animals [172-175]. Possible mechanisms include regulation of hippocampal glucocorticoid receptors or the restoration of dopamine levels in the reward centres in the brain [175]. Chronic mild stress in rats leads to increased corticosteroids, inflammatory markers and decreased anti-oxidant enzymes SOD and glutathione peroxidase and catalase in the hippocampus and prefrontal cortex. Simultaneous cholecalciferol treatment reverses these stress-mediated effects [69,176].
Chronic unpredictable stress increases immobility in a widely used test of behavioural despair (tail suspension test). Cholecalciferol treatment reduces this stress-induced immobility. Inhibiting the synthesis of the neurotransmitter serotonin abolishes cholecalciferol's actions in this test, suggesting vitamin D might act via increased serotonin synthesis [177]. Support for this idea comes from studies in glioblastoma cells showing functional VDREs are localised at —7 kb and -10 kb upstream of the serotonin, synthesising enzyme tryptophan hydroxylase [178]. Other studies chronically administering corticosterone replicate the cholecalciferol's reversal of these stress-induced behaviours and suggest either alterations to glucocorticoid signalling in the brain or reductions in stress-associated ROS production in the brain are the protective mechanisms [172,179]. Stress can be measured in animals using other behavioural paradigms such as immobility in a forced swim test. Chronic unpredictable stress increases immobility in this test. Cholecalciferol supplementation reverses this immobility as well as reduces serum corticosterone/ACTH levels and increases BDNF and NT-3/NT-4 levels in the hippocampus [174].
DVD-deficiency may also alter maternal response to stress in rats [180] and mice [181] and can adversely affect maternal care [80], which is well-known to induce permanent changes in offspring stress-response [182]. The translational potential of these later findings is enhanced given that a randomised clinical trial showed that 50,000 IU of cholecalciferol alone every 2 weeks, or in combination with Omega 3 fatty acids (1 g/day), for 8 weeks significantly reduced anxiety and improved sleep quality in women of reproductive age with pre-diabetes and hypovitaminosis D [183].

Hypervitaminosis D and Adverse CNS Outcomes

While the role of hypovitaminosis D in brain function has been extensively investigated, the effect of hypervitaminosis D has received less attention. This is despite an inverted U-shaped cellular response to 1,25(OH)2D3 being frequently reported, i.e., both high and low levels of 1,25(OH)2D3 induce adverse outcomes. Hypervitaminosis D is rare in humans, generally resulting from excess vitamin D supplementation or diseases such as sarcoidosis that produces excess 1,25(OH)2D3 due to activated macrophages [184]. Though not focused on neurological conditions, an older review concluded "There is accumulating evidence that both high and low serum calcidiol concentrations are associated with an increased risk of chronic diseases" [185]. Hypervitaminosis D always results in hypercalcaemia, which may be toxic to brain function. Animal studies showed that high cholecalciferol intake, 25,000 IU/kg, for four consecutive days reduces brainwave activity [186]. Senescence- accelerated-mouse-phenotype (SAMP) strain-8 mice, an animal model of accelerated human ageing, showed a progressive increase in serum 25OHD3, which coexists with reduced cognitive function and increased capillary permeability [187]. Deleting Fibroblast growth factor (FGF-23) in mice increased CYP27B1 levels, leading to increased 1,25(OH)2D3 synthesis. FGF-23 null mice display early ageing, and deleting CYP27B1 delayed premature ageing [188]. Considering the risk of hypervitaminosis D, serum vitamin D levels should be monitored in clinical trials of vitamin D supplementation.

Conclusions and Future Challenges

Here we have provided an up-to-date summary of research detailing vitamin D turnover, synthesis genomic and non-genomic actions in the brain, neurons and nonneuronal cells. We advise caution when considering much of the prior literature employing either dietary restrictions which often produced hypo-calcaemia or the use of constitutive knock out models permanently reducing 1,25(OH)2D3 synthesis or impairing VDR signalling, as these models produce too many non-CNS effects to make brain-related outcomes interpretable. Although there are still strain and species differences when choosing a model organism, contemporary DVD- or AVD-deficient models in rodents do not produce hypocalcaemic offspring and continue to produce findings of apparent relevance to the fields of psychiatry and neurology.
Increasingly, epidemiological studies associate low levels of vitamin D either prenatally or at birth with psychiatric conditions such as autism and schizophrenia. The epidemiology for degenerative diseases as diverse as Alzheimer's disease, Parkinson's disease and multiple sclerosis all continue to indicate a role of optimal vitamin D status throughout life. This raises the possibility of simple dietary supplementation as an adjunct to current therapies. Although not practicably possible for developmental conditions with adult onset such as schizophrenia, this could eventually be considered in early onset psychiatric disorders, such as autism or ADHD, or for maintaining neural integrity in degenerative conditions via large placebo-controlled, randomised clinical supplementation trials.
We would also like to take this opportunity to highlight design issues in many observational studies opportunistically linking early-life vitamin D deficiency with psychiatric disorders. Most of the published observational epidemiological studies linking early-life vitamin D status with a psychiatric diagnosis never address reverse causality (the condition changes behaviours that lead to less sun exposure). By way of illustration, a very highprofile recent report in the New England Journal of Medicine showed all mental illnesses were associated with an increased risk in a general medical condition [189]. In other words, patients with psychiatric conditions are generally suffering from other conditions that will curtail behaviour perhaps altering diet, exercise and exposure to sunshine. We urge all future epidemiological studies that seek to examine the relationship between vitamin D and psychiatric or neurological conditions to rigorously control for the often-poor general health of patients. This, of course, is less of an issue for gestational (DVD-deficiency) exposures in otherwise healthy mothers.
Important data have emerged from a recent mendelian randomisation study examining gene pathways related to 25(OH)D3 blood concentrations. This study found no evidence that genetic factors involved in the synthesis of 25(OH)D3 were causal for psychiatric disorders [190]. We have interpreted this to mean any link between 25(OH)D3 levels and brain-related outcomes are likely to be solely driven by environmental factors.
Autism is perhaps the developmental brain disorder most regularly linked with DVD- deficiency. However, well-conducted studies refuting this link are now emerging. For the studies describing an inverse relationship between maternal vitamin D levels and autism, they all had mean 25(OH)D3 levels of <50 nM which is considered by some authors to represent a cut off for vitamin D deficiency [11-13,191]. Two recent studies have failed to find this inverse association [106,192]. So, at face value, this appears a failure to replicate previous studies. However, it is crucial to note that in these last two studies, the mean levels of 25(OH)D3 were actually very high (>70-80 nM) and there were very few individuals that were actually vitamin D-deficient, meaning the association could not be properly tested. These same six studies all used the same laboratory to analyse samples, so technical bias (so common amongst vitamin D studies in different populations) could be ruled out. This suggests a threshold effect rather than any continuous relationship between DVD-deficiency and autism. We highlight this particular relationship to illustrate some of the confusion regarding statements regarding potential causality between vitamin D and various brain-related clinical disorders.
The incidence of hypovitaminosis D in both pregnant women and their newborns and the general population remains concerning [193]. Clearly, more rigorous study design is required taking into consideration such issues to bring clarity to the future epidemiological studies. Better quality studies in the future are needed given the substantial emotional and financial burden psychiatric and neurological disorders place on the patient and community. The opportunity to use such a simple, safe and inexpensive intervention as vitamin D supplementation as treatment or as an adjunct to existing therapies in such disorders remains extremely attractive from a public health perspective.

Abbreviations
VDR, vitamin D receptor; PDIA3, Protein disulfide-isomerase A3; RXR, retinoid X receptor; L-VGCC, L-type voltage-gated calcium channel; Cavl, L-type voltage-gated calcium subunit 1; TRPV1, transient receptor potential vanilloid subfamily member 1; ROS, reactive oxygen species; iNOS, inducible nitric oxide synthetase; NO, nitric oxide; NF-kB, nuclear factor kappa-B; Nrf2, nuclear factor erythroid 2-related factor 2; GP, glutathione peroxidase; CAT, catalase; SOD, superoxide dismutase; HO-1, heme oxygenase; NGF, nerve growth factor; BDNF, brain-derived neurotrophic factor; GDNF, glial cell line-derived neurotrophic factor; NT-3, neurotrophin 3; NT-4, neurotrophin 4; GR, glucocorticoid receptor; CORT, corticosterone; TNFa, tumour necrosis factor a; IL-6, interlukin-6; IL-1B, interlukin-1 Beta. (Figure created from BioRender.com).

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References

1. Evans, R.M. The nuclear receptor superfamily: A rosetta stone for physiology. Mol. Endocrinol. 2005,19,1429-1438. [CrossRef] [PubMed]
2. McGrath, J.; Feron, F.; Eyles, D. Vitamin D: The neglected neurosteroid? Trends Neurosci. 2001,24, 570-572. [CrossRef]
3. Cui, X.; Gooch, H.; Petty, A.; McGrath, J.J.; Eyles, D. Vitamin D and the brain: Genomic and non-genomic actions. Mol. Cell. Endocrinol. 2017, 453,131-143. [CrossRef] [PubMed]
4. Pertile, R.; Kiltschewskij, D.G.; Geaghan, M.; Barnett, M.; Cui, X.; Cairns, M.J.; Eyles, D.W. Developmental vitamin D-deficiency increases the expression of microRNAs involved in dopamine neuron development. Brain Res. 2022,1789,147953. [CrossRef] [PubMed]
5. Ali, A.; Vasileva, S.; Langguth, M.; Alexander, S.; Cui, X.; Whitehouse, A.; McGrath, J.J.; Eyles, D. Deveopmental vitamin D deficiency produces behavioral phenotypes of relevance to autism in an animal model. Nutrients 2019, 11, 1187. [CrossRef] [PubMed]
6. Melcangi, R.C.; Panzica, G. Neuroactive steroids: An update of their roles in central and peripheral nervous system. Psychoneuroendocrinology 2009, 34, S1-S8. [CrossRef]
7. Eyles, D.W.; Burne, T.H.; McGrath, J.J. Vitamin D, effects on brain development, adult brain function and the links between low levels of vitamin D and neuropsychiatric disease. Front. Neuroendocrinol. 2013, 34, 47-64. [CrossRef]
8. McCann, J.C.; Ames, B.N. Is there convincing biological or behavioral evidence linking vitamin D deficiency to brain dysfunction? FASEB J. 2008,22,982-1001. [CrossRef]
9. McGrath, J.J.; Eyles, D.W.; Pedersen, C.B.; Anderson, C.; Ko, P.; Burne, T.H.; Norgaard-Pedersen, B.; Hougaard, D.M.; Mortensen, P.B. Neonatal vitamin D status and risk of schizophrenia: A population-based case-control study. Arch. Gen. Psychiatry 2010, 67, 889-894. [CrossRef]
10. Eyles, D.W.; Trzaskowski, M.; Vinkhuyzen, A.A.E.; Mattheisen, M.; Meier, S.; Gooch, H.; Anggono, V.; Cui, X.; Tan, M.C.; Burne, T.H.J.; et al. The association between neonatal vitamin D status and risk of schizophrenia. Sci. Rep. 2018, 8,17692. [CrossRef]
11. Vinkhuyzen, A.A.E.; Eyles, D.W.; Burne, T.H.J.; Blanken, L.M.E.; Kruithof, C.J.; Verhulst, F.; Jaddoe, V.W.; Tiemeier, H.; McGrath, J.J. Gestational vitamin D deficiency and autism-related traits: The Generation R study. Mol. Psychiatry 2016, 23, 240-246. [CrossRef] [PubMed]
12. Vinkhuyzen, A.; Eyles, D.; Burne, T.; Blanken, L.; Kruithof, C.; Verhulst, F.; White, T.; Jaddoe, V.W.; Tiemeier, H.; McGrath, J. Gestational Vitamin D Deficiency and Autism Spectrum Disorder. Br. J. Psychiatry Open 2017, 3, 85-90. [CrossRef] [PubMed]
13. Lee, B.K.; Eyles, D.W.; Magnusson, C.; Newschaffer, C.J.; McGrath, J.J.; Kvaskoff, D.; Ko, P.; Dalman, C.; Karlsson, H.; Gardner, R.M. Developmental vitamin D and autism spectrum disorders: Findings from the Stockholm Youth Cohort. Mol. Psychiatry 2019, 26,1578-1588. [CrossRef] [PubMed]
14. Sourander, A.; Upadhyaya, S.; Surcel, H.M.; Hinkka-Yli-Salomaki, S.; Cheslack-Postava, K.; Silwal, S.; Sucksdorff, M.; McKeague, I.W.; Brown, A.S. Maternal Vitamin D Levels During Pregnancy and Offspring Autism Spectrum Disorder. Biol. Psychiatry 2021, 90, 790-797. [CrossRef] [PubMed]
15. Strnm, M.; Halldorsson, T.; Hansen, S.; Granstrom, C.; Maslova, E.; Petersen, S.B.; Cohen, A.S.; Olsen, S.F. Vitamin D measured in maternal serum and offspring neurodevelopmental outcomes: A prospective study with long-term follow-up. Ann. Nutr. Metab. 2014, 64, 254-261. [CrossRef]
16. Morales, E.; Julvez, J.; Torrent, M.; Ballester, F.; Rodríguez-Bernal, C.L.; Andiarena, A.; Vegas, O.; Castilla, A.M.; Rodriguez-Dehli, C.; Tardón, A.; et al. Vitamin D in Pregnancy and Attention Deficit Hyperactivity Disorder-like Symptoms in Childhood. Epidemiology 2015, 26, 458-465. [CrossRef]
17. Arns, M.; van der Heijden, K.B.; Arnold, L.E.; Kenemans, J.L. Geographic variation in the prevalence of ateention- deficit/hyperactivity disorder: The sunny perspective. Biol. Psychiatry 2013, 74, 585-590. [CrossRef]
18. Groves, N.; McGrath, J.; Burne, T. Adult vitamin D deficiency and adverse Brain Outcomes. In Vitamin D Vol 2 Health, Disease and Therapeutics, 4th ed.; Feldman, D., Ed.; Elsevier: London, UK, 2018; Volume 1, pp. 1147-1158.
19. Cui, X.; McGrath, J.J.; Burne, T.H.J.; Eyles, D.W. Vitamin D and schizophrenia: 20 years on. Mol. Psychiatry 2021, 26, 2708-2720. [CrossRef]
20. Holmoy, T.; Moen, S.M.; Gundersen, T.A.; Holick, M.F.; Fainardi, E.; Castellazzi, M.; Casetta, I. 25-hydroxyvitamin D in cerebrospinal fluid during relapse and remission of multiple sclerosis. Mult. Scler. 2009,15,1280-1285. [CrossRef]
21. Balabanova, S.; Richter, H.P.; Antoniadis, G.; Homoki, J.; Kremmer, N.; Hanle, J.; Teller, W.M. 25-Hydroxyvitamin D, 24, 25-dihydroxyvitamin D and 1,25-dihydroxyvitamin D in human cerebrospinal fluid. Klin. Wochenschr. 1984, 62, 1086-1090. [CrossRef]
22. Ahonena, L.; Maireb, F.B.R.; Savolainenc, S.; Koprac, J.; Vreekenb, R.J.; Hankemeierb, T.; Myohanenc, T.; Kyllia, P.; Kostiainena, R. Analysis of oxysterols and vitamin D metabolites in mouse brain and cell line samples by ultra-high-performance liquid chromatography-atmospheric pressure photoionization-mass spectrometry. J. Chromatogr. A 2014,1364, 214-222. [CrossRef] [PubMed]
23. Xue, Y.; He, X.; Li, H.-D.; Deng, Y.; Yan, M.; Cai, H.-L.; Tang, M.-M.; Dang, R.-L.; Jiang, P. Simultaneous quantification of 25-Hydroxyvitamin D3 and 24,25-dihydroxyvitamin D3 in rats shows strong correlations between serum and brain tissue levels. Int. J. Endocrinol. 2015,2015, 296531. [CrossRef] [PubMed]
24. Fu, X.; Dolnikowski, G.G.; Patterson, W.B.; Dawson-Hughes, B.; Zheng, T.; Morris, M.C.; Holland, T.M.; Booth, S.L. Determination of Vitamin D and Its Metabolites in Human Brain Using an Ultra-Pressure LC-Tandem Mass Spectra Method. Curr. Dev. Nutr. 2019, 3, nzz074. [CrossRef] [PubMed]
25. Eyles, D.W.; Smith, S.; Kinobe, R.; Hewison, M.; McGrath, J.J. Distribution of the vitamin D receptor and 1 alpha-hydroxylase in human brain. J. Chem. Neuroanat. 2005, 29, 21-30. [CrossRef]
26. Prufer, K.; Jirikowski, G.F. 1.25-Dihydroxyvitamin D3 receptor is partly colocalized with oxytocin immunoreactivity in neurons of the male rat hypothalamus. Cell. Mol. Biol. 1997, 43, 543-548.
27. Clemens, T.L.; McGlade, S.A.; Garrett, K.P.; Horiuchi, N.; Hendy, G.N. Tissue-specific regulation of avian vitamin D-dependent calcium-binding protein 28-kDa mRNA by 1,25-dihydroxyvitamin D3. J. Biol. Chem. 1988, 263,13112-13116. [CrossRef]
28. Prufer, K.; Veenstra, T.D.; Jirikowski, G.F.; Kumar, R. Distribution of 1,25-dihydroxyvitamin D3 receptor immunoreactivity in the rat brain and spinal cord. J. Chem. Neuroanat. 1999,16,135-145. [CrossRef]
29. Walbert, T.; Jirikowski, G.F.; Prufer, K. Distribution of 1,25-dihydroxyvitamin D3 receptor immunoreactivity in the limbic system of the rat. Horm. Metab. Res. 2001, 33, 525-531. [CrossRef]
30. Craig, T.A.; Sommer, S.; Sussman, C.R.; Grande, J.P.; Kumar, R. Expression and regulation of the vitamin D receptor in the zebrafish, Danio rerio. J. Bone Miner. Res. 2008, 23,1486-1496. [CrossRef]
31. Wang, Y.; Becklund, B.R.; DeLuca, H.F. Identification of a highly specific and versatile vitamin D receptor antibody. Arch. Biochem. Biophys. 2010, 494,166-177. [CrossRef]
32. Wang, Y.; DeLuca, H.F. Is the vitamin D receptor found in muscle? Endocrinology 2011,152, 354-363. [CrossRef] [PubMed]
33. Eyles, D.W.; Liu, P.Y.; Josh, P.; Cui, X. Intracellular distribution of the vitamin D receptor in the brain: Comparison with classic target tissues and redistribution with development. Neuroscience 2014, 268,1-9. [CrossRef] [PubMed]
34. Stumpf, W.E.; O'Brien, L.P. 1,25 (OH)2 vitamin D3 sites of action in the brain. An autoradiographic study. Histochemistry 1987, 87, 393-406. [CrossRef] [PubMed]
35. Cui, X.; Pelekanos, M.; Liu, P.Y.; Burne, T.H.J.; McGrath, J.J.; Eyles, D. The vitamin D receptor in dopamine neurons; its presence in human substantia nigra and its ortogenesis in rat midbrain. Neuroscience 2013, 236, 77-87. [CrossRef]
36. Veenstra, T.D.; Prufer, K.; Koenigsberger, C.; Brimijoin, S.W.; Grande, J.P.; Kumar, R. 1,25-Dihydroxyvitamin D3 receptors in the central nervous system of the rat embryo. Brain Res. 1998, 804,193-205. [CrossRef]
37. Burkert, R.; McGrath, J.; Eyles, D. Vitamin D receptor expression in the embryonic rat brain. Neurosci. Res. Commun. 2003, 33, 63-71. [CrossRef]
38. Erben, R.G.; Soegiarto, D.W.; Weber, K.; Zeitz, U.; Lieberherr, M.; Gniadecki, R.; Moller, G.; Adamski, J.; Balling, R. Deletion of deoxyribonucleic acid binding domain of the vitamin D receptor abrogates genomic and nongenomic functions of vitamin D. Mol. Endocrinol. 2002,16,1524-1537. [CrossRef]
39. Cui, X.; McGrath, J.J.; Burne, T.H.; Mackay-Sim, A.; Eyles, D.W. Maternal vitamin D depletion alters neurogenesis in the developing rat brain. Int. J. Dev. Neurosci. 2007,25, 227-232. [CrossRef]
40. Liu, H.; He, Y.; Beck, J.; da Silva Teixeira, S.; Harrison, K.; Xu, Y.; Sisley, S. Defining vitamin D receptor expression in the brain using a novel VDR(Cre) mouse. J. Comp. Neurol. 2021, 529, 2362-2375. [CrossRef]
41. Fu, G.K.; Lin, D.; Zhang, M.Y.; Bikle, D.D.; Shackleton, C.H.; Miller, W.L.; Portale, A.A. Cloning of human 25-hydroxyvitamin D-1 alpha-hydroxylase and mutations causing vitamin D-dependent rickets type 1. Mol. Endocrinol. 1997,11,1961-1970.
42. Zehnder, D.; Bland, R.; Williams, M.C.; McNinch, R.W.; Howie, A.J.; Stewart, P.M.; Hewison, M. Extrarenal expression of 25-hydroxyvitamin d(3)-1 alpha-hydroxylase. J. Clin. Endocrinol. Metab. 2001, 86, 888-894. [PubMed]
43. Landel, V.; Stephan, D.; Cui, X.; Eyles, D.; Feron, F. Differential expression of vitamin D-associated enzymes and receptors in brain cell subtypes. J. Steroid Biochem. Mol. Biol. 2018,177, 129-134. [CrossRef] [PubMed]
44. Naveilhan, P.; Neveu, I.; Baudet, C.; Ohyama, K.Y.; Brachet, P.; Wion, D. Expression of 25(OH) vitamin D3 24-hydroxylase gene in glial cells. Neuroreport 1993, 5, 255-257. [CrossRef] [PubMed]
45. Hendrix, I.; Anderson, P.; May, B.; Morris, H. Regulation of gene expression by the CYP27B1 promoter-study of a transgenic mouse model. J. Steroid Biochem. Mol. Biol. 2004, 89,139-142. [CrossRef] [PubMed]
46. Eyles, D.W.; McGrath, J.J. Vitamin D brain development and function. In Vitamin D Vol 1 Biochemistry, Physiology and Diagnostics; Feldman, D., Ed.; Elsevier: London, UK, 2018; Volume 1, pp. 563-581.
47. Eyles, D.W. Vitamin D: Brain and Behavior. JBMR Plus 2021, 5, e10419. [CrossRef]
48. Brown, J.; Bianco, J.I.; McGrath, J.J.; Eyles, D.W. 1,25-dihydroxyvitamin D3 induces nerve growth factor, promotes neurite outgrowth and inhibits mitosis in embryonic rat hippocampal neurons. Neurosci. Lett. 2003, 343,139-143. [CrossRef]
49. Marini, F.; Bartoccini, E.; Cascianelli, G.; Voccoli, V.; Baviglia, M.G.; Magni, M.V.; Garcia-Gil, M.; Albi, E. Effect of 1alpha,25- dihydroxyvitamin D3 in embryonic hippocampal cells. Hippocampus 2010, 20, 696-705. [CrossRef]
50. Horst, R.L.; Napoli, J.L.; Littledike, E.T. Discrimination in the metabolism of orally dosed ergocalciferol and cholecalciferol by the pig, rat and chick. Biochem. J. 1982, 204,185-189. [CrossRef]
51. Chabas, J.F.; Alluin, O.; Rao, G.; Garcia, S.; Lavaut, M.N.; Risso, J.J.; Legre, R.; Magalon, G.; Khrestchatisky, M.; Marqueste, T.; et al. Vitamin D2 potentiates axon regeneration. J. Neurotrauma 2008,25,1247-1256. [CrossRef]
52. Ribeiro, M.C.; Moore, S.M.; Kishi, N.; Macklis, J.D.; MacDonald, J.L. Vitamin D Supplementation Rescues Aberrant NF-kappaB Pathway Activation and Partially Ameliorates Rett Syndrome Phenotypes in Mecp2 Mutant Mice. eNeuro 2020, 7. [CrossRef]
53. Tague, S.E.; Smith, P.G. Vitamin D deficiency leads to sensory and sympathetic denervation of the rat synovium. Neuroscience 2014, 279, 77-93. [CrossRef] [PubMed]
54. Feron, F.; Marqueste, T.; Bianco, J.; Gueye, Y.; Chabas, J.F.; Decherchi, P. Repairing the spinal cord with vitamin D: A promising strategy. Biol. Aujourdhui 2014, 208, 69-75. [CrossRef] [PubMed]
55. Neveu, I.; Naveilhan, P.; Jehan, F.; Baudet, C.; Wion, D.; De Luca, H.F.; Brachet, P. 1,25-dihydroxyvitamin D3 regulates the synthesis of nerve growth factor in primary cultures of glial cells. Brain Res. Mol. Brain Res. 1994, 24, 70-76. [CrossRef]
56. Wion, D.; MacGrogan, D.; Neveu, I.; Jehan, F.; Houlgatte, R.; Brachet, P. 1,25-Dihydroxyvitamin D3 is a potent inducer of nerve growth factor synthesis. J. Neurosci. Res. 1991,28,110-114. [CrossRef]
57. Neveu, I.; Naveilhan, P.; Baudet, C.; Brachet, P.; Metsis, M. 1,25-dihydroxyvitamin D3 regulates NT-3, NT-4 but not BDNF mRNA in astrocytes. Neuroreport 1994, 6,124-126. [CrossRef]
58. Dursun, E.; Gezen-Ak, D.; Yilmazer, S. A novel perspective for Alzheimer's disease: Vitamin D receptor suppression by amyloidbeta and preventing the amyloid-beta induced alterations by vitamin D in cortical neurons. J. Alzheimers. Dis. 2011, 23, 207-219. [CrossRef]
59. Gezen-Ak, D.; Dursun, E.; Yilmazer, S. The Effects of Vitamin D Receptor Silencing on the Expression of LVSCC-A1C and LVSCC-A1D and the Release of NGF in Cortical Neurons. PLoS ONE 2011, 6, e17553. [CrossRef]
60. Saporito, M.S.; Wilcox, H.M.; Hartpence, K.C.; Lewis, M.E.; Vaught, J.L.; Carswell, S. Pharmacological induction of nerve growth factor mRNA in adult rat brain. Exp. Neurol. 1993,123, 295-302. [CrossRef]
61. Granholm, A.C.; Reyland, M.; Albeck, D.; Sanders, L.; Gerhardt, G.; Hoernig, G.; Shen, L.; Westphal, H.; Hoffer, B. Glial cell line-derived neurotrophic factor is essential for postnatal survival of midbrain dopamine neurons. J. Neurosci. 2000, 20,3182-3190. [CrossRef]
62. Oo, T.F.; Burke, R.E. The time course of developmental cell death in phenotypically defined dopaminergic neurons of the substantia nigra. Brain Res. Dev. Brain Res. 1997, 98,191-196. [CrossRef]
63. Shirazi, H.A.; Rasouli, J.; Ciric, B.; Rostami, A.; Zhang, G.X. 1,25-Dihydroxyvitamin D3 enhances neural stem cell proliferation and oligodendrocyte differentiation. Exp. Mol. Pathol. 2015, 98, 240-245. [CrossRef] [PubMed]
64. Orme, R.P.; Bhangal, M.S.; Fricker, R.A. Calcitriol imparts neuroprotection in vitro to midbrain dopaminergic neurons by upregulating GDNF expression. PLoS ONE 2013, 23, e62040. [CrossRef] [PubMed]
65. Pertile, R.; Cui, X.; Hammond, L.A.; Eyles, D.W. Vitamin D regulation of GDNF/Ret signaling in dopaminergic neurons. FASEB J. 2018, 32, 819-828. [CrossRef] [PubMed]
66. Eyles, D.; Brown, J.; Mackay-Sim, A.; McGrath, J.; Feron, F. Vitamin D3 and brain development. Neuroscience 2003,118, 641-653. [CrossRef]
67. Hawes, J.E.; Tesic, D.; Whitehouse, A.J.; Zosky, G.R.; Smith, J.T.; Wyrwoll, C.S. Maternal vitamin D deficiency alters fetal brain development in the BALB/c mouse. Behav. Brain Res. 2015, 286,192-200. [CrossRef]
68. Abdollahzadeh, M.; Panahpour, H.; Ghaheri, S.; Saadati, H. Calcitriol supplementation attenuates cisplatin-induced behavioral and cognitive impairments through up-regulation of BDNF in male rats. Brain Res. Bull. 2022,181, 21-29. [CrossRef]
69. Bakhtiari-Dovvombaygi, H.; Izadi, S.; Zare, M.; Asgari Hassanlouei, E.; Dinpanah, H.; Ahmadi-Soleimani, S.M.; Beheshti, F. Vitamin D3 administration prevents memory deficit and alteration of biochemical parameters induced by unpredictable chronic mild stress in rats. Sci. Rep. 2021,11,16271. [CrossRef]
70. Mansouri, F.; Ghanbari, H.; Marefati, N.; Arab, Z.; Salmani, H.; Beheshti, F.; Hosseini, M. Protective effects of vitamin D on learning and memory deficit induced by scopolamine in male rats: The roles of brain-derived neurotrophic factor and oxidative stress. Naunyn-Schmiedeberg's Arch. Pharmacol. 2021, 394,1451-1466. [CrossRef]
71. Bayat, M.; Kohlmeier, K.A.; Haghani, M.; Haghighi, A.B.; Khalili, A.; Bayat, G.; Hooshmandi, E.; Shabani, M. Co-treatment of vitamin D supplementation with enriched environment improves synaptic plasticity and spatial learning and memory in aged rats. Psychopharmacology 2021,238, 2297-2312. [CrossRef]
72. Tan, X.; Gao, L.; Cai, X.; Zhang, M.; Huang, D.; Dang, Q.; Bao, L. Vitamin D3 alleviates cognitive impairment through regulating inflammatory stress in db/db mice. Food Sci. Nutr. 2021, 9, 4803-4814. [CrossRef]
73. Manjari, S.K.V.; Maity, S.; Poornima, R.; Yau, S.Y.; Vaishali, K.; Stellwagen, D.; Komal, P. Restorative Action of Vitamin D3 on Motor Dysfunction Through Enhancement of Neurotrophins and Antioxidant Expression in the Striatum. Neuroscience 2022, 492,67-81. [CrossRef] [PubMed]
74. Cui, X.; Pelekanos, M.; Burne, T.H.; McGrath, J.J.; Eyles, D.W. Maternal vitamin D deficiency alters the expression of genes involved in dopamine specification in the developing rat mesencephalon. Neurosci. Lett. 2010, 486, 220-223. [CrossRef] [PubMed]
75. Luan, W.; Hammond, L.A.; Cotter, E.; Osborne, G.W.; Alexander, S.A.; Nink, V.; Cui, X.; Eyles, D.W. Developmental Vitamin D (DVD) Deficiency Reduces Nurr1 and TH Expression in Post-mitotic Dopamine Neurons in Rat Mesencephalon. Mol. Neurobiol. 2018, 55, 2243-2453. [CrossRef] [PubMed]
76. Kesby, J.P.; Cui, X.; Ko, P.; McGrath, J.J.; Burne, T.H.; Eyles, D.W. Developmental vitamin D deficiency alters dopamine turnover in neonatal rat forebrain. Neurosci. Lett. 2009, 461,155-158. [CrossRef] [PubMed]
77. Luan, W.; Hammond, L.A.; Vuillermot, S.; Meyer, U.; Eyles, D.W. Maternal vitamin D prevents abnormal dopaminergic development and function in a mouse model of prenatal immune activation. Sci. Rep. 2018, 8, 9741. [CrossRef] [PubMed]
78. Cui, X.; Pertile, R.; Liu, P.; Eyles, D.W. Vitamin D regulates tyrosine hydroxylase expression: N-cadherin a possible mediator. Neuroscience 2015, 304, 90-100. [CrossRef]
79. Pertile, R.A.N.; Cui, X.; Eyles, D.W. Vitamin D signalling and the differentiation of developing dopamine systems. Neuroscience 2016, 333,193-203. [CrossRef]
80. Yates, N.J.; Tesic, D.; Feindel, K.W.; Smith, J.T.; Clarke, M.W.; Wale, C.; Crew, R.C.; Wharfe, M.; Whitehouse, A.J.; Wyrwoll, C.S. Vitamin D is crucial for maternal care and offspring social behaviour in rats. J. Endocrinol. 2018, 237, 73-85. [CrossRef]
81. Ali, A.A.; Cui, X.; Pertile, R.A.N.; Li, X.; Medley, G.; Alexander, S.A.; Whitehouse, A.J.O.; McGrath, J.J.; Eyles, D.W. Developmental vitamin D deficiency increases foetal exposure to testosterone. Mol. Autism. 2020,11, 96. [CrossRef]
82. Xu, X.J.; Shou, X.J.; Li, J.; Jia, M.X.; Zhang, J.S.; Guo, Y.; Wei, Q.Y.; Zhang, X.T.; Han, S.P.; Zhang, R.; et al. Mothers of autistic children: Lower plasma levels of oxytocin and Arg-vasopressin and a higher level of testosterone. PLoS ONE 2013, 8, e74849. [CrossRef]
83. Burne, T.H.; Becker, A.; Brown, J.; Eyles, D.W.; Mackay-Sim, A.; McGrath, J.J. Transient prenatal Vitamin D deficiency is associated with hyperlocomotion in adult rats. Behav. Brain Res. 2004,154, 549-555. [CrossRef]
84. Kesby, J.P.; Burne, T.H.; McGrath, J.J.; Eyles, D.W. Developmental vitamin D deficiency alters MK 801-induced hyperlocomotion in the adult rat: An animal model of schizophrenia. Biol. Psychiatry 2006, 60, 591-596. [CrossRef]
85. Kesby, J.P.; O'Loan, J.C.; Alexander, S.; Deng, C.; Huang, X.F.; McGrath, J.J.; Eyles, D.W.; Burne, T.H. Developmental vitamin D deficiency alters MK-801-induced behaviours in adult offspring. Psychopharmacology 2012, 220, 455-463. [CrossRef]
86. O'Loan, J.; Eyles, D.W.; Kesby, J.; Ko, P.; McGrath, J.J.; Burne, T.H. Vitamin D deficiency during various stages of pregnancy in the rat; its impact on development and behaviour in adult offspring. Psychoneuroendocrinology 2007, 32, 227-234. [CrossRef]
87. Kesby, J.P.; Cui, X.; O'Loan, J.; McGrath, J.J.; Burne, T.H.; Eyles, D.W. Developmental vitamin D deficiency alters dopaminemediated behaviors and dopamine transporter function in adult female rats. Psychopharmacology 2010,208,159-168. [CrossRef]
88. Becker, A.; Grecksch, G. Pharmacological treatment to augment hole board habituation in prenatal Vitamin D-deficient rats. Behav. Brain Res. 2006,166,177-183. [CrossRef]
89. Grecksch, G.; Ruthrich, H.; Hollt, V.; Becker, A. Transient prenatal vitamin D deficiency is associated with changes of synaptic plasticity in the dentate gyrus in adult rats. Psychoneuroendocrinology 2009, 34, S258-S264. [CrossRef]
90. Becker, A.; Eyles, D.W.; McGrath, J.J.; Grecksch, G. Transient prenatal vitamin D deficiency is associated with subtle alterations in learning and memory functions in adult rats. Behav. Brain Res. 2005,161, 306-312. [CrossRef]
91. Turner, K.M.; Young, J.W.; McGrath, J.J.; Eyles, D.W.; Burne, T.H.J. Cognitive performance and response inhibition in developmentally vitamin D (DVD)-deficient rats. Behav. Brain Res. 2013, 242, 47-53. [CrossRef]
92. Overeem, K.; Alexander, S.; Burne, T.H.J.; Ko, P.; Eyles, D.W. Developmental Vitamin D Deficiency in the Rat Impairs Recognition Memory, but Has No Effect on Social Approach or Hedonia. Nutrients 2019,11, 2713. [CrossRef]
93. Vuillermot, S.; Luan, W.; Meyer, U.; Eyles, D. Vitamin D treatment during pregnancy prevents autism-related phenotypes in a mouse model of maternal immune activation. Mol. Autism. 2017, 8, 9. [CrossRef]
94. Kazemi, F.; Babri, S.; Keyhanmehr, P.; Farid-Habibi, M.; Rad, S.N.; Farajdokht, F. Maternal vitamin D supplementation and treadmill exercise attenuated vitamin D deficiency-induced anxiety-and depressive-like behaviors in adult male offspring rats. Nutr. Neurosci. 2022,1-13. [CrossRef] [PubMed]
95. Schoenrock, S.A.; Tarantino, L.M. Deveopmental vitamin D deficiency and schizophrenia: The role of animal models. Genes Brain Behav. 2016,15, 45-61. [CrossRef] [PubMed]
96. Harms, L.H.; Turner, K.M.; Eyles, D.W.; Young, J.W.; McGrath, J.J.; BUrne, T.H.J. Attentional processing in C57BL/6J mice exposed to developmental vitamin D deficiency. PLoS ONE 2012, 7, e35896.
97. Harms, L.R.; Eyles, D.W.; McGrath, J.J.; Mackay-Sim, A.; Burne, T.H. Developmental vitamin D deficiency alters adult behaviour in 129/SvJ and C57BL/6J mice. Behav. Brain Res. 2008,187, 343-350. [CrossRef] [PubMed]
98. Harms, L.H.; Cowin, G.; Eyles, D.W.; Kurniawan, N.; McGrath, J.J.; Burne, T.H.J. Neuroanatomy and psychomimetic-induced locomotion in C57BL/6J and 129/X1SvJ mice exposed to developmental vitamin D deficiency. Behav. Brain Res. 2012, 230,125-131. [CrossRef]
99. Hart, P.H.; Lucas, R.M.; Walsh, J.P.; Zosky, G.R.; Whitehouse, A.J.; Zhu, K.; Allen, K.L.; Kusel, M.M.; Anderson, D.; Mountain, J.A. Vitamin D in fetal development: Findings from a birth cohort study. Pediatrics 2015,135, e167-e173. [CrossRef]
100. Voltas, N.; Canals, J.; Hernandez-Martinez, C.; Serrat, N.; Basora, J.; Arija, V. Effect of Vitamin D Status during Pregnancy on Infant Neurodevelopment: The ECLIPSES Study. Nutrients 2020,12, 3196. [CrossRef]
101. Mutua, A.M.; Mogire, R.M.; Elliott, A.M.; Williams, T.N.; Webb, E.L.; Abubakar, A.; Atkinson, S.H. Effects of vitamin D deficiency on neurobehavioural outcomes in children: A systematic review. Wellcome Open Res. 2020, 5, 28. [CrossRef]
102. Arrhenius, B.; Upadhyaya, S.; Hinkka-Yli-Salomaki, S.; Brown, A.S.; Cheslack-Postava, K.; Ohman, H.; Sourander, A. Prenatal Vitamin D Levels in Maternal Sera and Offspring Specific Learning Disorders. Nutrients 2021,13, 3321. [CrossRef]
103. Wicklow, B.; Gallo, S.; Majnemer, A.; Vanstone, C.; Comeau, K.; Jones, G.; L'Abbe, M.; Khamessan, A.; Sharma, A.; Weiler, H.; et al. Impact of Vitamin D Supplementation on Gross Motor Development of Healthy Term Infants: A Randomized Dose-Response Trial. Phys. Occup. Ther. Pediatr. 2016, 36, 330-342. [CrossRef] [PubMed]
104. Whitehouse, A.J.; Holt, B.J.; Serralha, M.; Holt, P.G.; Kusel, M.M.; Hart, P.H. Maternal serum vitamin D levels during pregnancy and offspring neurocognitive development. Pediatrics 2012,129, 485-493. [CrossRef] [PubMed]
105. Hanieh, S.; Ha, T.T.; Simpson, J.A.; Thuy, T.T.; Khuong, N.C.; Thoang, D.D.; Tran, T.D.; Tuan, T.; Fisher, J.; Biggs, B.A. Maternal vitamin D status and infant outcomes in rural Vietnam: A prospective cohort study. PLoS ONE 2014, 9, e99005. [CrossRef] [PubMed]
106. Schmidt, R.J.; Niu, Q.; Eyles, D.W.; Hansen, R.L.; Iosif, A.M. Neonatal vitamin D status in relation to autism spectrum disorder and developmental delay in the CHARGE case-control study. Autism. Res. 2019,12, 976-988. [CrossRef] [PubMed]
107. Lopez-Vicente, M.; Sunyer, J.; Lertxundi, N.; Gonzalez, L.; Rodriguez-Dehli, C.; Espada Saenz-Torre, M.; Vrijheid, M.; Tardon, A.; Llop, S.; Torrent, M.; et al. Maternal circulating Vitamin D3 levels during pregnancy and behaviour across childhood. Sci. Rep. 2019, 9,14792. [CrossRef]
108. Sass, L.; Vinding, R.K.; Stokholm, J.; Bjarnadottir, E.; Noergaard, S.; Thorsen, J.; Sunde, R.B.; McGrath, J.; Bonnelykke, K.; Chawes, B.; et al. High-Dose Vitamin D Supplementation in Pregnancy and Neurodevelopment in Childhood: A Prespecified Secondary Analysis of a Randomized Clinical Trial. JAMA Netw. Open 2020, 3, e2026018. [CrossRef]
109. Li, B.; Xu, Y.; Zhang, X.; Zhang, L.; Wu, Y.; Wang, X.; Zhu, C. The effect of vitamin D supplementation in treatment of children with autism spectrum disorder: A systematic review and meta-analysis of randomized controlled trials. Nutr. Neurosci. 2022, 25, 835-845. [CrossRef]
110. Dehbokri, N.; Noorazar, G.; Ghaffari, A.; Mehdizadeh, G.; Sarbakhsh, P.; Ghaffary, S. Effect of vitamin D treatment in children with attention-deficit hyperactivity disorder. World J. Pediatr. 2019,15, 78-84. [CrossRef]
111. Elshorbagy, H.H.; Barseem, N.F.; Abdelghani, W.E.; Suliman, H.A.I.; Al-Shokary, A.H.; Abdulsamea, S.E.; Elsadek, A.E.; Abdel Maksoud, Y.H.; Nour El Din, D. Impact of Vitamin D Supplementation on Attention-Deficit Hyperactivity Disorder in Children. Ann. Pharmacother. 2018, 52,623-631. [CrossRef]
112. Miller, M.C.; Pan, X.; Eugene Arnold, L.; Mulligan, A.; Connor, S.; Bergman, R.; deBeus, R.; Roley-Roberts, M.E. Vitamin D levels in children with attention deficit hyperactivity disorder: Association with seasonal and geographical variation, supplementation, inattention severity, and theta:beta ratio. Biol. Psychol. 2021,162,108099. [CrossRef]
113. Mohammadpour, N.; Jazayeri, S.; Tehrani-Doost, M.; Djalali, M.; Hosseini, M.; Effatpanah, M.; Davari-Ashtiani, R.; Karami, E. Effect of vitamin D supplementation as adjunctive therapy to methylphenidate on ADHD symptoms: A randomized, double blind, placebo-controlled trial. Nutr. Neurosci. 2018, 21, 202-209. [CrossRef] [PubMed]
114. Zhou, P.; Wolraich, M.L.; Cao, A.H.; Jia, F.Y.; Liu, B.; Zhu, L.; Liu, Y.; Li, X.; Li, C.; Peng, B.; et al. Adjuvant effects of vitamin A and vitamin D supplementation on treatment of children with attention-deficit/hyperactivity disorder: A study protocol for a randomised, double-blinded, placebo-controlled, multicentric trial in China. BMJ Open 2021,11, e050541. [CrossRef] [PubMed]
115. Pilz, S.; Trummer, C.; Theiler-Schwetz, V.; Grubler, M.R.; Verheyen, N.D.; Odler, B.; Karras, S.N.; Zittermann, A.; Marz, W. Critical Appraisal of Large Vitamin D Randomized Controlled Trials. Nutrients 2022,14, 303. [CrossRef] [PubMed]
116. Suzuki, M.; Yoshioka, M.; Hashimoto, M.; Murakami, M.; Noya, M.; Takahashi, D.; Urashima, M. Randomized, double-blind, placebo-controlled trial of vitamin D supplementation in Parkinson disease. Am. J. Clin. Nutr. 2013, 97,1004-1013. [CrossRef]
117. Kang, J.H.; Vyas, C.M.; Okereke, O.I.; Ogata, S.; Albert, M.; Lee, I.M.; D'Agostino, D.; Buring, J.E.; Cook, N.R.; Grodstein, F.; et al. Effect of vitamin D on cognitive decline: Results from two ancillary studies of the VITAL randomized trial. Sci. Rep. 2021, 11, 23253. [CrossRef]
118. Feige, J.; Moser, T.; Bieler, L.; Schwenker, K.; Hauer, L.; Sellner, J. Vitamin D Supplementation in Multiple Sclerosis: A Critical Analysis of Potentials and Threats. Nutrients 2020,12, 783. [CrossRef]
119. Lieberherr, M. Effects of vitamin D3 metabolites on cytosolic free calcium in confluent mouse osteoblasts. J. Biol. Chem. 1987, 262,13168-13173. [CrossRef]
120. Caffrey, J.M.; Farach-Carson, M.C. Vitamin D3 metabolites modulate dihydropyridine-sensitive calcium currents in clonal rat osteosarcoma cells. J. Biol. Chem. 1989,264, 20265-20274. [CrossRef]
121. Ibi, M.; Sawada, H.; Nakanishi, M.; Kume, T.; Katsuki, H.; Kaneko, S.; Shimohama, S.; Akaike, A. Protective effects of 1 alpha,25- (OH)(2)D-3 against the neurotoxicity of glutamate and reactive oxygen species in mesencephalic culture. Neuropharmacology 2001, 40, 761-771. [CrossRef]
122. Brewer, L.D.; Thibault, V.; Chen, K.C.; Langub, M.C.; Landfield, P.W.; Porter, N.M. Vitamin D hormone confers neuroprotection in parallel with downregulation of L-type calcium channel expression in hippocampal neurons. J. Neurosci. 2001, 21, 98-108. [CrossRef]
123. Gezen-Ak, D.; Dursun, E.; Yilmazer, S. Vitamin D inquiry in hippocampal neurons: Consequences of vitamin D-VDR pathway disruption on calcium channel and the vitamin D requirement. Neurol. Sci. 2013, 34,1453-1458. [CrossRef] [PubMed]
124. Zanatta, L.; Goulart, P.B.; Gongalves, R.; Pierozan, P.; Winkelmann-Duarte, E.C.; Woehl, V.M.; Pessoa-Pureur, R.; Silva, F.R.; Zamoner, A. 1 a,25-dihydroxyvitamin D(3) mechanism of action: Modulation of L-type calcium channels leading to calcium uptake and intermediate filament phosphorylation in cerebral cortex of young rats. Biochim. Biophys. Acta 2012,1823,1708-1719. [CrossRef] [PubMed]
125. Gooch, H.; Cui, X.; Anggono, V.; Trzaskowski, M.; Tan, M.C.; Eyles, D.W.; Burne, T.H.J.; Jang, S.E.; Mattheisen, M.; Hougaard, D.M.; et al. 1,25-Dihydroxyvitamin D modulates L-type voltage-gated calcium channels in a subset of neurons in the developing mouse prefrontal cortex. Transl. Psychiatry 2019, 9, 281. [CrossRef]
126. Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nature 2014, 511, 421-427. [CrossRef] [PubMed]
127. Long, W.; Fatehi, M.; Soni, S.; Panigrahi, R.; Philippaert, K.; Yu, Y.; Kelly, R.; Boonen, B.; Barr, A.; Golec, D.; et al. Vitamin D is an endogenous partial agonist of the transient receptor potential vanilloid 1 channel. J. Physiol. 2020, 598, 4321-4338. [CrossRef] [PubMed]
128. Holick, M.F. Vitamin D deficiency. N. Engl. J. Med. 2007, 357, 266-281. [CrossRef]
129. Almeida Moreira Leal, L.K.; Lima, L.A.; Alexandre de Aquino, P.E.; Costa de Sousa, J.A.; Jatai Gadelha, C.V.; Felicio Calou, I.B.; Pereira Lopes, M.J.; Viana Lima, F.A.; Tavares Neves, K.R.; Matos de Andrade, G.; et al. Vitamin D (VD3) antioxidative and anti-inflammatory activities: Peripheral and central effects. Eur. J. Pharmacol. 2020, 879,173099. [CrossRef]
130. Uberti, F.; Morsanuto, V.; Bardelli, C.; Molinari, C. Protective effects of 1 a,25-Dihydroxyvitamin D3 on cultured neural cells exposed to catalytic iron. Physiol. Rep. 2016, 4, e12769. [CrossRef]
131. Chen, K.B.; Lin, A.M.; Chiu, T.H. Systemic vitamin D3 attenuated oxidative injuries in the locus coeruleus of rat brain. Ann. N. Y. Acad. Sci. 2003, 993, 313-324; discussion 345-349. [CrossRef]
132. Lin, A.M.; Fan, S.F.; Yang, D.M.; Hsu, L.L.; Yang, C.H. Zinc-induced apoptosis in substantia nigra of rat brain: Neuroprotection by vitamin D3. Free Radic. Biol. Med. 2003, 34,1416-1425. [CrossRef]
133. Kasatkina, L.A.; Tarasenko, A.S.; Krupko, O.O.; Kuchmerovska, T.M.; Lisakovska, O.O.; Trikash, I.O. Vitamin D deficiency induces the excitation/inhibition brain imbalance and the proinflammatory shift. Int. J. Biochem. Cell Biol. 2020, 119,105665. [CrossRef] [PubMed]
134. Garcion, E.; Nataf, S.; Berod, A.; Darcy, F.; Brachet, P. 1,25-Dihydroxyvitamin D3 inhibits the expression of inducible nitric oxide synthase in rat central nervous system during experimental allergic encephalomyelitis. Brain Res. Mol. Brain Res. 1997, 45, 255-267. [CrossRef]
135. Garcion, E.; Sindji, L.; Montero-Menei, C.; Andre, C.; Brachet, P.; Darcy, F. Expression of inducible nitric oxide synthase during rat brain inflammation: Regulation by 1,25-dihydroxyvitamin D3. Glia 1998, 22, 282-294. [CrossRef]
136. Lefebvre d'Hellencourt, C.; Montero-Menei, C.N.; Bernard, R.; Couez, D. Vitamin D3 inhibits proinflammatory cytokines and nitric oxide production by the EOC13 microglial cell line. J. Neurosci. Res. 2003, 71, 575-582. [CrossRef] [PubMed]
137. Hur, J.; Lee, P.H.; Kim, M.J.; Cho, Y.-W. Regulatory effect of 25-hydroxyvitamin D3 on nitric oxide production in activated microglia. Korean J. Physiol. Pharmacol. 2014,18, 397-402. [CrossRef]
138. Huang, Y.; Ho, Y.; Lai, C.; Chiu, C.; Wang, Y. 1,25-dihydroxyvitamin D3 attenuates endotoxin-induced production of inflammatory mediators by inhibiting MAPK activation in primary cortical neuron-glia cultures. J. Neuroinflammation 2015,12,147. [CrossRef]
139. Loginova, M.; Mishchenko, T.; Savyuk, M.; Guseva, S.; Gavrish, M.; Krivonosov, M.; Ivanchenko, M.; Fedotova, J.; Vedunova, M. Double-Edged Sword of Vitamin D3 Effects on Primary Neuronal Cultures in Hypoxic States. Int. J. Mol. Sci. 2021, 22,5417. [CrossRef]
140. Ali, A.; Cui, X.; Alexander, S.; Eyles, D. The placental immune response is dysregulated developmentally vitamin D deficient rats: Relevance to autism. J. Steroid. Biochem. Mol. Biol. 2018,180, 73-80. [CrossRef]
141. Alessio, N.; Belardo, C.; Trotta, M.C.; Paino, S.; Boccella, S.; Gargano, F.; Pieretti, G.; Ricciardi, F.; Marabese, I.; Luongo, L.; et al. Vitamin D Deficiency Induces Chronic Pain and Microglial Phenotypic Changes in Mice. Int. J. Mol. Sci. 2021, 22,3604. [CrossRef]
142. Rastegar-Moghaddam, S.H.; Hosseini, M.; Alipour, F.; Rajabian, A.; Ebrahimzadeh Bideskan, A. The effects of vitamin D on learning and memory of hypothyroid juvenile rats and brain tissue acetylcholinesterase activity and oxidative stress indicators. Naunyn-Schmiedeberg's Arch. Pharmacol. 2022, 395,337-351. [CrossRef]
143. Mokhtari-Zaer, A.; Hosseini, M.; Salmani, H.; Arab, Z.; Zareian, P. Vitamin D3 attenuates lipopolysaccharide-induced cognitive impairment in rats by inhibiting inflammation and oxidative stress. Life Sci. 2020,253,117703. [CrossRef] [PubMed]
144. Xu, M.L.; Yu, X.J.; Zhao, J.Q.; Du, Y.; Xia, W.J.; Su, Q.; Du, M.M.; Yang, Q.; Qi, J.; Li, Y.; et al. Calcitriol ameliorated autonomic dysfunction and hypertension by down-regulating inflammation and oxidative stress in the paraventricular nucleus of SHR. Toxicol. Appl. Pharmacol. 2020, 394,114950. [CrossRef] [PubMed]
145. Khassafi, N.; Zahraei, Z.; Vahidinia, Z.; Karimian, M.; Azami Tameh, A. Calcitriol Pretreatment Attenuates Glutamate Neurotoxicity by Regulating NMDAR and CYP46A1 Gene Expression in Rats Subjected to Transient Middle Cerebral Artery Occlusion. J. Neuropathol. Exp. Neurol. 2022, 81, 252-259. [CrossRef]
146. Vahidinia, Z.; Khassafi, N.; Tameh, A.A.; Karimian, M.; Zare-Dehghanani, Z.; Moradi, F.; Joghataei, M.T. Calcitriol Ameliorates Brain Injury in the Rat Model of Cerebral Ischemia-Reperfusion Through Nrf2/HO-1 Signalling Axis: An in Silico and in Vivo Study. J. Stroke Cerebrovasc. Dis. 2022, 31,106331. [CrossRef] [PubMed]
147. Filomeni, G.; De Zio, D.; Cecconi, F. Oxidative stress and autophagy: The clash between damage and metabolic needs. Cell Death Differ. 2015, 22, 377-388. [CrossRef] [PubMed]
148. Bhowmick, S.; D'Mello, V.; Caruso, D.; Abdul-Muneer, P.M. Traumatic brain injury-induced downregulation of Nrf2 activates inflammatory response and apoptotic cell death. J. Mol. Med. 2019, 97,1627-1641. [CrossRef] [PubMed]
149. Cui, C.; Wang, C.; Jin, F.; Yang, M.; Kong, L.; Han, W.; Jiang, P. Calcitriol confers neuroprotective effects in traumatic brain injury by activating Nrf2 signaling through an autophagy-mediated mechanism. Mol. Med. 2021, 27,118. [CrossRef]
150. Hosseinirad, H.; Shahrestanaki, J.K.; Moosazadeh Moghaddam, M.; Mousazadeh, A.; Yadegari, P.; Afsharzadeh, N. Protective Effect of Vitamin D3 Against Pb-Induced Neurotoxicity by Regulating the Nrf2 and NF-kappaB Pathways. Neurotox. Res. 2021, 39, 687-696. [CrossRef]
151. Jiang, H.; Zhang, S. Therapeutic effect of acute and chronic use of different doses of vitamin D3 on seizure responses and cognitive impairments induced by pentylenetetrazole in immature male rats. Iran. J. Basic Med. Sci. 2022, 25, 84-95. [CrossRef]
152. Bayo-Olugbami, A.; Nafiu, A.B.; Amin, A.; Ogundele, O.M.; Lee, C.C.; Owoyele, B.V. Vitamin D attenuated 6-OHDA-induced behavioural deficits, dopamine dysmetabolism, oxidative stress, and neuro-inflammation in mice. Nutr. Neurosci. 2022, 25, 823-834. [CrossRef]
153. Lima, L.A.R.; Lopes, M.J.P.; Costa, R.O.; Lima, F.A.V.; Neves, K.R.T.; Calou, I.B.F.; Andrade, G.M.; Viana, G.S.B. Vitamin D protects dopaminergic neurons against neuroinflammation and oxidative stress in hemiparkinsonian rats. J. Neuroinflammation 2018, 15, 249. [CrossRef] [PubMed]
154. Hu, J.; Wu, J.; Wan, F.; Kou, L.; Yin, S.; Sun, Y.; Li, Y.; Zhou, Q.; Wang, T. Calcitriol Alleviates MPP(+)- and MPTP-Induced Parthanatos Through the VDR/PARP1 Pathway in the Model of Parkinson's Disease. Front. Aging Neurosci. 2021,13, 657095. [CrossRef] [PubMed]
155. Fan, Y.G.; Pang, Z.Q.; Wu, T.Y.; Zhang, Y.H.; Xuan, W.Q.; Wang, Z.; Yu, X.; Li, Y.C.; Guo, C.; Wang, Z.Y. Vitamin D deficiency exacerbates Alzheimer-like pathologies by reducing antioxidant capacity. Free Radic. Biol. Med. 2020,161,139-149. [CrossRef] [PubMed]
156. Mehrabadi, S.; Sadr, S.S. Administration of Vitamin D3 and E supplements reduces neuronal loss and oxidative stress in a model of rats with Alzheimer's disease. Neurol. Res. 2020, 42, 862-868. [CrossRef] [PubMed]
157. Grimm, M.O.W.; Lauer, A.A.; Grosgen, S.; Thiel, A.; Lehmann, J.; Winkler, J.; Janitschke, D.; Herr, C.; Beisswenger, C.; Bals, R.; et al. Profiling of Alzheimer's disease related genes in mild to moderate vitamin D hypovitaminosis. J. Nutr. Biochem. 2019, 67,123-137. [CrossRef]
158. Lin, F.Y.; Lin, Y.F.; Lin, Y.S.; Yang, C.M.; Wang, C.C.; Hsiao, Y.H. Relative D3 vitamin deficiency and consequent cognitive impairment in an animal model of Alzheimer's disease: Potential involvement of collapsin response mediator protein-2. Neuropharmacology 2020,164,107910. [CrossRef]
159. Lin, C.I.; Chang, Y.C.; Kao, N.J.; Lee, W.J.; Cross, T.W.; Lin, S.H. 1,25(OH)2D3 Alleviates Abeta(25-35)-Induced Tau Hyperphosphorylation, Excessive Reactive Oxygen Species, and Apoptosis Through Interplay with Glial Cell Line-Derived Neurotrophic Factor Signaling in SH-SY5Y Cells. Int. J. Mol. Sci. 2020,21, 4215. [CrossRef] [PubMed]
160. De Oliveira, L.R.C.; Mimura, L.A.N.; Fraga-Silva, T.F.C.; Ishikawa, L.L.W.; Fernandes, A.A.H.; Zorzella-Pezavento, S.F.G.; Sartori, A. Calcitriol Prevents Neuroinflammation and Reduces Blood-Brain Barrier Disruption and Local Macrophage/Microglia Activation. Front. Pharmacol. 2020,11,161. [CrossRef]
161. Shirazi, H.A.; Rasouli, J.; Ciric, B.; Wei, D.; Rostami, A.; Zhang, G.X. 1,25-Dihydroxyvitamin D3 suppressed experimental autoimmune encephalomyelitis through both immunomodulation and oligodendrocyte maturation. Exp. Mol. Pathol. 2017, 102,515-521. [CrossRef]
162. Nystad, A.E.; Wergeland, S.; Aksnes, L.; Myhr, K.M.; Bo, L.; Torkildsen, O. Effect of high-dose 1.25 dihydroxyvitamin D3 on remyelination in the cuprizone model. APMIS 2014,122,1178-1186. [CrossRef]
163. Paintlia, M.K.; Singh, I.; Singh, A.K. Effect of vitamin D3 intake on the onset of disease in a murine model of human Krabbe disease. J. Neurosci. Res. 2015, 93, 28-42. [CrossRef] [PubMed]
164. Sapolsky, R.M. Stress, Glucocorticoids, and Damage to the Nervous System: The Current State of Confusion. Stress 1996,1,1-19. [CrossRef] [PubMed]
165. Chen, T.L.; Cone, C.M.; Morey-Holton, E.; Feldman, D. Glucocorticoid regulation of 1,25(OH)2-vitamin D3 receptors in cultured mouse bone cells. J. Biol. Chem. 1982,257,13564-13569. [CrossRef]
166. Chen, T.L.; Cone, C.M.; Morey-Holton, E.; Feldman, D. 1 alpha,25-dihydroxyvitamin D3 receptors in cultured rat osteoblast-like cells. Glucocorticoid treatment increases receptor content. J. Biol. Chem. 1983, 258, 4350-4355. [CrossRef]
167. Neveu, I.; Barbot, N.; Jehan, F.; Wion, D.; Brachet, P. Antagonistic effects of dexamethasone and 1,25-dihydroxyvitamin D3 on the synthesis of nerve growth factor. Mol. Cell. Endocrinol. 1991, 78, R1-R6. [CrossRef]
168. Neveu, I.; Jehan, F.; Wion, D. Alteration in the levels of 1,25-(OH)2D3 and corticosterone found in experimental diabetes reduces nerve growth factor (NGF) gene expression in vitro. Life Sci. 1992, 50,1769-1772. [CrossRef]
169. Lundqvist, J.; Norlin, M.; Wikvall, K. 1alpha,25-Dihydroxyvitamin D3 affects hormone production and expression of steroidogenic enzymes in human adrenocortical NCI-H295R cells. Biochim. Biophys. Acta 2010,1801,1056-1062. [CrossRef]
170. Obradovic, D.; Gronemeyer, H.; Lutz, B.; Rein, T. Cross-talk of vitamin D and glucocorticoids in hippocampal cells. J. Neurochem. 2006, 96, 500-509. [CrossRef]
171. Jiang, P.; Xue, Y.; Li, H.D.; Liu, Y.P.; Cai, H.L.; Tang, M.M.; Zhang, L.H. Dysregulation of vitamin D metabolism in the brain and myocardium of rats following prolonged exposure to dexamethasone. Psychopharmacology 2014, 231, 3345-3351. [CrossRef] [PubMed]
172. Camargo, A.; Dalmagro, A.P.; Platt, N.; Rosado, A.F.; Neis, V.B.; Zeni, A.L.B.; Kaster, M.P.; Rodrigues, A.L.S. Cholecalciferol abolishes depressive-like behavior and hippocampal glucocorticoid receptor impairment induced by chronic corticosterone administration in mice. Pharmacol. Biochem. Behav. 2020,196,172971. [CrossRef]
173. Camargo, A.; Dalmagro, A.P.; Rikel, L.; da Silva, E.B.; Simao da Silva, K.A.B.; Zeni, A.L.B. Cholecalciferol counteracts depressive- like behavior and oxidative stress induced by repeated corticosterone treatment in mice. Eur. J. Pharmacol. 2018, 833, 451-461. [CrossRef] [PubMed]
174. Koshkina, A.; Dudnichenko, T.; Baranenko, D.; Fedotova, J.; Drago, F. Effects of Vitamin D3 in Long-Term Ovariectomized Rats Subjected to Chronic Unpredictable Mild Stress: BDNF, NT-3, and NT-4 Implications. Nutrients 2019,11,1726. [CrossRef] [PubMed]
175. Sedaghat, K.; Yousefian, Z.; Vafaei, A.A.; Rashidy-Pour, A.; Parsaei, H.; Khaleghian, A.; Choobdar, S. Mesolimbic dopamine system and its modulation by vitamin D in a chronic mild stress model of depression in the rat. Behav. Brain Res. 2019, 356,156-169. [CrossRef] [PubMed]
176. Sedaghat, K.; Naderian, R.; Pakdel, R.; Bandegi, A.R.; Ghods, Z. Regulatory effect of vitamin D on pro-inflammatory cytokines and anti-oxidative enzymes dysregulations due to chronic mild stress in the rat hippocampus and prefrontal cortical area. Mol. Biol. Rep. 2021, 48, 7865-7873. [CrossRef]
177. Neis, V.B.; Werle, I.; Moretti, M.; Rosa, P.B.; Camargo, A.; de, O. Dalsenter, Y.; Platt, N.; Rosado, A.F.; Engel, W.D.; de Almeida, G.R.L.; et al. Involvement of serotonergic neurotransmission in the antidepressant-like effect elicited by cholecalciferol in the chronic unpredictable stress model in mice. Metab. Brain Dis. 2022, 37,1597-1608. [CrossRef]
178. Kaneko, I.; Sabir, M.S.; Dussik, C.M.; Whitfield, G.K.; Karrys, A.; Hsieh, J.C.; Haussler, M.R.; Meyer, M.B.; Pike, J.W.; Jurutka, P.W. 1,25-Dihydroxyvitamin D regulates expression of the tryptophan hydroxylase 2 and leptin genes: Implication for behavioral influences of vitamin D. FASEB J. 2015, 29, 4023-4035. [CrossRef]
179. Da Silva Souza, S.V.; da Rosa, P.B.; Neis, V.B.; Moreira, J.D.; Rodrigues, A.L.S.; Moretti, M. Effects of cholecalciferol on behavior and production of reactive oxygen species in female mice subjected to corticosterone-induced model of depression. Naunyn- Schmiedeberg's Arch. Pharmacol. 2020, 393,111-120. [CrossRef]
180. Eyles, D.W.; Rogers, F.; Buller, K.; McGrath, J.J.; Ko, P.; French, K.; Burne, T.H. Developmental vitamin D (DVD) deficiency in the rat alters adult behaviour independently of HPA function. Psychoneuroendocrinology 2006, 31, 958-964. [CrossRef]
181. Tesic, D.; Hawes, J.E.; Zosky, G.R.; Wyrwoll, C.S. Vitamin D Deficiency in BALB/c Mouse Pregnancy Increases Placental Transfer of Glucocorticoids. Endocrinology 2015,156, 3673-3679. [CrossRef]
182. Meaney, M.J. Maternal care, gene expression, and the transmission of individual differences in stress reactivity across generations. Annu. Rev. Neurosci. 2001, 24,1161-1192. [CrossRef]
183. Rajabi-Naeeni, M.; Dolatian, M.; Qorbani, M.; Vaezi, A.A. Effect of omega-3 and vitamin D co-supplementation on psychological distress in reproductive-aged women with pre-diabetes and hypovitaminosis D: A randomized controlled trial. Brain Behav. 2021 e2342. [CrossRef] [PubMed]
184. Tebben, P.J.; Singh, R.J.; Kumar, R. Vitamin D-Mediated Hypercalcemia: Mechanisms, Diagnosis, and Treatment. Endocr. Rev. 2016, 37, 521-547. [CrossRef] [PubMed]
185. Tuohimaa, P.; Keisala, T.; Minasyan, A.; Cachat, J.; Kalueff, A. Vitamin D, nervous system and aging. Psychoneuroendocrinology 2009, 34, S278-S286. [CrossRef] [PubMed]
186. Lima, G.O.; Menezes da Silva, A.L.; Azevedo, J.E.C.; Nascimento, C.P.; Vieira, L.R.; Hamoy, A.O.; Oliveira Ferreira, L.; Bahia, V.; Muto, N.A.; Lopes, D.C.F.; et al. 100 YEARS of VITAMIN D: Supraphysiological doses of vitamin D changes brainwave activity patterns in rats. Endocr. Connect. 2022,11, e210457. [CrossRef] [PubMed]
187. Lam, V.; Takechi, R.; Mano, J. Vitamin D, Cerebrocapillary Integrity and Cognition in Murine Model of Accelerated Ageing. Alzheimer's Dement. 2017,13,1304. [CrossRef]
188. Razzaque, M.S.; Sitara, D.; Taguchi, T.; St-Arnaud, R.; Lanske, B. Premature aging-like phenotype in fibroblast growth factor 23 null mice is a vitamin D-mediated process. FASEB J. 2006, 20, 720-722. [CrossRef]
189. Momen, N.C.; Plana-Ripoll, O.; Agerbo, E.; Benros, M.E.; Borglum, A.D.; Christensen, M.K.; Dalsgaard, S.; Degenhardt, L.; de Jonge, P.; Debost, J.P.G.; et al. Association between Mental Disorders and Subsequent Medical Conditions. N. Engl. J. Med. 2020, 382,1721-1731. [CrossRef]
190. Revez, J.A.; Lin, T.; Qiao, Z.; Xue, A.; Holtz, Y.; Zhu, Z.; Zeng, J.; Wang, H.; Sidorenko, J.; Kemper, K.E.; et al. Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Nat. Commun. 2020,11,1647. [CrossRef]
191. Wu, D.M.; Wen, X.; Han, X.R.; Wang, S.; Wang, Y.J.; Shen, M.; Fan, S.H.; Zhuang, J.; Li, M.Q.; Hu, B.; et al. Relationship between Neonatal Vitamin D at Birth and Risk of Autism Spectrum Disorders: The NBSIB Study. J. Bone Miner. Res. 2018, 33, 458-466. [CrossRef]
192. Windham, G.C.; Pearl, M.; Anderson, M.C.; Poon, V.; Eyles, D.; Jones, K.L.; Lyall, K.; Kharrazi, M.; Croen, L.A. Newborn vitamin D levels in relation to autism spectrum disorders and intellectual disability: A case-control study in california. Autism. Res. 2019, 989-998. [CrossRef]
193. Saraf, R.; Morton, S.M.B.; Camargo, C.A.J.; Grant, C.C. Global summary of maternal and newborn vitamin D status—A systematic review. Matern. Child Nutr. 2016,12, 647-668. [CrossRef] [PubMed]

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Brain and Vitamin D chart - 2023

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Microglia and Brain Disorders: The Role of Vitamin D and Its Receptor - July 2023

Int J Mol Sci. 2023 Jul 25;24(15):11892. doi: 10.3390/ijms241511892.
Alessandra Mirarchi 1, Elisabetta Albi 2, Tommaso Beccari 2, Cataldo Arcuri 1

Accounting for 5-20% of the total glial cells present in the adult brain, microglia are involved in several functions: maintenance of the neural environment, response to injury and repair, immunesurveillance, cytokine secretion, regulation of phagocytosis, synaptic pruning, and sculpting postnatal neural circuits.
Microglia contribute to some neurodevelopmental disorders, such as

• Nasu-Hakola disease (NHD),
• Tourette syndrome (TS),
• autism spectrum disorder (ASD), and
• schizophrenia.

Moreover, microglial involvement in neurodegenerative diseases, such as

• Alzheimer's (AD) and
• Parkinson's (PD) diseases,

has also been well established. During the last two decades, epidemiological and research studies have demonstrated the involvement of vitamin D3 (VD3) in the brain's pathophysiology. VD3 is a fat-soluble metabolite that is required for the proper regulation of many of the body's systems, as well as for normal human growth and development, and shows neurotrophic and neuroprotective actions and influences on neurotransmission and synaptic plasticity, playing a role in various neurological diseases. In order to better understand the exact mechanisms behind the diverse actions of VD3 in the brain, a large number of studies have been performed on isolated cells or tissues of the central nervous system (CNS). Here, we discuss the involvement of VD3 and microglia on neurodegeneration- and aging-related diseases.

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Conclusions

Microglia have long been considered to be a key player in the health of the CNS and, to a lesser extent, of other non-parenchymal immune cells 148. Microglia are directly and indirectly involved in the onset of many CNS diseases (Scheme 1), and treatments modulat­ing microglial function could be performed as new complementary therapeutic strategies in CNS diseases. However, since microglia are able to take different phenotypes—not only pro-inflammatory M1 and anti-inflammatory M2, but also a multitude of intermediate states—this goal is complex.
During aging, the loss of microglial functions is progressive, and this phenomenon causes a de facto increasing inflammatory state. If the microglial phenotypes control these processes in the brain, it is reasonable to think that the modulation of microglial activity, by limiting inflammation, could generate positive effects for brain functions. In this context, the administration of nutrients with an anti-inflammatory action in the diet makes sense.
As regards the role of calcitriol in the brain, some data are now consolidated. This role involves microglia, inter alia, and appears to be a clear anti-inflammatory role, re­ducing the production of inflammatory cytokines (which could have a protective effect in preventing inflammation and excessive inflammatory reactions), but also playing a role in neuroprotection. Activated microglia produce inflammatory mediator species that can damage neurons. VD3 may reduce the production of these harmful substances and promote neuronal function and survival. Furthermore, in vitro studies have suggested that VD3 promotes the differentiation of precursor cells in mature microglia, influencing their activation state. This could be important in the immune responses and outcomes of inflammation in the CNS.
While the roles of microglia in various CNS diseases are known (Scheme 1), the role of VD3 in the treatment of these pathologies is less clear. In the brain, VD3 has been involved in multiple sclerosis, sleep disorders, autism spectrum disorder, Parkinson's disease, and Alzheimer's disease. It should be noted that microglia are involved in all of these pathologies.
Unfortunately, treatments for these diseases with VD3 have not been conclusive, and other trials are required to fully understand its role.
The question of whether the continuous administration of VD3 in the diet can prevent the onset of CNS pathologies remains to be considered. For example, a recent study [149] demonstrated that high VD3 levels in multiple sclerosis (MS) patients reduced the risk of relapses. Since, most MS patients present low levels of VD3, VD3 supplementation is now a common practice. However, the question of whether VD3 administration prevents the onset of MS or is beneficial to patients remains unresolved. More generally, VD3 can play a complementary role in the prevention and management of neurological diseases.
Additional investigations will be necessary to evaluate the neuroprotective and thera­peutic potential of VD3 in promoting healthy brain aging and preventing neurodegeneration.
 Download the PDF from Vitamin D Life

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It appears that a fetus with adequate Vitamin D will have fewer brain problems

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It appears that an adult with adequate Vitamin D will have fewer brain problems

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Vitamin D Life - Brain development needs Vitamin D from week 3 thru 39

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Vitamin D Life - How Vitamin D fights Alzheimer’s, Parkinson’s, Multiple Sclerosis and Epilepsy – June 2023

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Vitamin D Life - Central Nervous System protection by Vitamin D - Dec 2023

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Vitamin D Life - Cerebral Palsy and Vitamin D - many studies has

Vitamin D Life - Ensure a healthy pregnancy and baby - take Vitamin D before conception has:

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Vitamin D Life - Overview Alzheimer's-Cognition and Vitamin D contains

• FACT: Cognitive decline is 19X more likely if low vitamin D
• FACT: Dementia is associated with low vitamin D levels.
• FACT: Alzheimer’s Dementia 2.3X more likely in elderly if low vitamin D – Dec 2022
• FACT: Dementia is associated with low vitamin D - many studies
• FACT: Alzheimer's Disease is 4X less likely if high vitamin D
• FACT: Every single risk factor listed for Alzheimer's Disease is also a risk factor for low vitamin D levels
• FACT: Elderly cognition gets worse as the elderly vitamin D levels get even lower (while in senior homes)
• OBSERVATION: Reports of increased vitamin D levels result in improved cognition
• OBSERVATION: Alzheimer’s patients 3X more likely to have a malfunctioning vitamin D receptor gene – 2012
• OBSERVATION: Alzheimer's Disease has been seen to halt when vitamin D was added.
• OBSERVATION: Alzheimer’s is associated with all 7 of the genes which restrict vitamin D
• OBSERVATION: 39 vitamin D and Alz. or Cognition intervention trials as of Sept 2018
• OBSERVATION: 2 Meta-analysis in 2012 agreed that Alzheimer's Disease. associated with low vitamin D
• OBSERVATION: 50X increase in Alzheimer's while decrease in vitamin D
• OBSERVATION: Vitamin D reduces Alzheimer’s disease in 11 ways
• OBSERVATION: Alzheimer’s cognition improved by 4,000 IU of vitamin D
• OBSERVATION: Plaque removed in mice by equiv. of 14,000 IU daily
• OBSERVATION: DDT (which decreases Vit D) increases risk of Alzheimer's by up to 3.8X
• OBSERVATION: 2% of people have 2 copies of the poor gene reference: Alz Org
• OBSERVATION: Genes do not change rapidly enough to account for the huge increase in incidence
• OBSERVATION: End of Alzheimer's videos, transcripts and many studies protocol has been very successful
  • It adjusts Vitamin D, B-12, Iron, Omega-3, food, etc, and can now be done at home.
• FACT: Vitamin D is extremely low cost and has very very few side effects
• CONCLUSION: Everyone concerned about cognitive decline or Alzheimer's Disease should take vitamin D
• PREDICTION MET: By 2024 Omega-3 and high dose Vitamin D will be found to reverse Alzheimer's in humans
  There are 13+ Alzheimer’s meta-analyses in Vitamin D Life
  There are 97+ Alzheimer’s studies in Vitamin D Life
  Dementia is associated with low vitamin D - many studies 50+ studies
  16+ studies in both categories Cognitive and Omega-3

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Vitamin D Life - Cognitive category contains

Very brief summary of Cognitive decline
Treatment : Vitamin D intervention slows or stops progression
Prevention : Many observational studies - perhaps Vitamin D prevents
Omega-3 both prevents and treats cognition
Wonder the benefits if both Vitamin D AND Omega-3 were to be used
Dementia page - 50 items

373 items in Cognition category

see also Overview Alzheimer's-Cognition and Vitamin D
Overview Parkinson's and Vitamin D

Studies in both categories of Cognition and:
Cardiovascular (7 studies), Genetics (9 studies), Vitamin D Receptor (16 studies), Omega-3 (49 studies), Intervention (19 studies), Meta-analyses (22 studies), Depression (23 studies), Parkinson's (22 studies)
Click here for details

Poor cognition 26 percent more likely if low Vitamin D (29 studies) – meta-analysis July 2017
Every schizophrenia measure was improved when vitamin D levels were normalized – June 2021
Cognitive Impairment and Dementia often associated with low Vitamin D – April 2020
IQ levels around the world are falling (perhaps lower Vitamin D, Iodine, or Omega-3)
Search Vitamin D Life for "WHITE MATTER" 325 items as of March 2023

Types of evidence that Vitamin D helps brain problems - 2014

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Vitamin D Life - Overview MS and vitamin D contains

Clinical interventions have shown that Vitamin D can prevent, treat, and even cure Multiple Sclerosis, at a tiny fraction of the cost of the drugs now used to treat it, and without side effects.

• Fact: Low Vitamin D results in higher risk of getting MS
  Increase latitude leads to decreased Vitamin D, which leads to increased risk of MS
  
  
  There is less of an effect recently - air conditioning now allows people to stay indoors

  
  
  Dark skinned people are far more likely to get MS (dark skin people typically have low vitamin D)
  Elderly (who typically have low vitamin D) are more likely to get MS
  Is there increased risk in people who already have diseases associated with low vitamin D - TB, for example ? ? ?
  Women typically have 3X increased MS risk then men (note: women typically have 20% lower levels of vitamin D than men)
     Exception: women in very sunny climates and dark-skinned women have the same MS risk as men
  Obese are 60% more likely to get MS
  Multiple Sclerosis 42X more likely if light brown skin and smoke (both associated with low vitamin D) – July 2020
  MS recurrence is much higher in spring - the lowest time of the year for vitamin D
  increase in clouds/rainfall (which reduces available Vitamin D) is associated with increased risk of MS (Scotland, Western Washington)
  MS incidence has increased 70% in a decade while the incidence of vitamin D deficiency doubled
  Less MS in those with outdoor occupations PDF file, not a web page
• Fact: MS uses up Vitamin D
• Fact: Lower vitamin D (due to MS using up Vitamin D while fighting the disease) results in many other health problems (such as broken bones), so depleted vitamin D levels must be restored.
  
  Fact: Increasing levels of Vitamin D is associated with lower MS risk, as well as lower risk of many other diseases

  
• Fact: Vitamin D looks so promising for preventing and treating MS that there were 25 INTERVENTION clinical trials as of Feb 2014
• Fact: Vitamin D reduced the MS relapse rate far better than Fingolimod which is now used for that purpose.
  • Note: Fingolimod costs $25,000/year while vitamin D, which works better and has no side effects is 1000 times less expensive.
• Fact: 98% of the genes affected by Interferon are also affected by Vitamin D
  • Note: 1 week of Interferon = $4,700, 1 week of vitamin D 10,000X lower cost
• Fact: MS Doctors in Brazil recommending 40-100 ng/mL of Vitamin D
• Fact: Many MS forums are recommending vitamin D to treat MS, with some taking 5,000 to 10,000 IU daily
  Observation: Risk of going from pre-MS to MS reduced 68 percent with 7100 IU vitamin D – RCT Dec 2012
  • This is an observation instead of a fact - it has not yet been confirmed.
• Fact: VERY LARGE doses of vitamin D have CURED 2,000 people of MS in Brazil
• Controversy: UVB fron sunlight or UVB bulb may be BETTER than Vitamin D for reducing the risk of getting MS
• Hypothesis: In addition to Vitamin D there are many other photoproducts produced by UVB that may promote health.

Summary: lack of consensus on how much to prevent, treat, or cure MS.

• How much Vitamin D to prevent many diseases - such as MS
• How much Vitamin D is needed to treat MS? There is currently no agreement
     The recommendations range from 40 to 100 ng - which can result of a dose ranging from 3,000 to 20,000 IU/day
• How Vitamin D is needed to Cure MS?: It appears that 20,000-140,000 IU daily may be needed to CURE the disease
     You must be under the supervision of a doctor who knows what to watch for in your individual situation.
     High doses of Vitamin D cannot be used as a monotherapy.
     You will need to adjust the cofactors: Typically increasing Magnesium and Vitamin K2, and reducing Calcium intake.
     Your doctor will monitor these and might increase your intake of Vitamins B2, C, as well as Omega-3899
• Epstein-Barr virus increases risk of Multiple Sclerosis by 32X - Jan 2022
• Multiple Sclerosis treated by Vitamin D, recommends investigating high dose Coimbra - Oct 2021
• Multiple Sclerosis patients had fewer COVID-19 problems (Note: many MSers take Vitamin D) – April 30, 2021
• Vitamin D Resistance hypothesis confirmed by Coimbra high-dose vitamin D protocol – April 2021
• Multiple Sclerosis relapses cut in half by 100,000 IU of Vitamin D every 2 weeks– RCT 2019

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Vitamin D Life - Cerebral Palsy and Vitamin D - many studies

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Vitamin D Life - Autism category contains

Autism category has 155 items

 - see also Overview Autism and vitamin D,  Autoimmune ,   Cognitive,    ADHD
Interesting Autistic studies
Autism associated with low Vitamin D

• Most Autism Risk factors are associated with low vitamin D - March 2014
• Rickets – 26 percent had autism: no rickets, no autism (both associated with low vitamin D) – June 2015
• Premature birth 2.5X more likely if mother had low vitamin D and was having twins – July 2013
• Autism 3X more likely after closely spaced pregnancy vs 3 year apart– Jan 2011
• Having twins takes more vitamin D - May 2011

Autism treated by Vitamin D

• Autism treated by Vitamin D (monthly injection of 150,000 IU) – June 2017
• Autism decreased in 8 out of 10 children supplemented with vitamin D – April 2015

Autism reduced by vitamins before and during pregnancy

• Autism reduced 24% for each 4 ng more Vitamin D while pregnant ( ADHD 12%) – Feb 2024
• Low maternal Vitamin D results in larger portion of brain associated with autism – Jan 2020
• Autism risk reduced 2X by prenatal vitamins (Vitamin D or Folic) – Feb 2019
• Low Vitamin D decreases fertility and increases subsequent autism, ADHD, etc – Feb 2018
• Women who had supplemented with any vitamins were 6 X less likely to have autistic offspring – Jan 2018
• Autism rate cut in half when multivitamins (including vitamin D) used during pregnancy – Oct 2017
• Autism rate in siblings reduced 4X by vitamin D: 5,000 IU during pregnancy, 1,000 IU to infants – Feb 2016

Autism and Vitamin D Receptor (not enough Vit D gets to the cells)
This list is automatically updated

Autism - other risk factors

• Autistic symptoms reduced by Vitamin D and or Omega-3 – RCT March 2019
• Omega-3 probably can decrease Autism and ADHD – March 2019
• Autism risk increased if infant had antibiotics (2X), acetaminophen (3X), or no vitamin D drops (1.5X) – June 2018
• 20 X more Parkinson's and 100X more Autism with GMO soy in China
  • Note >100X increase in Autism while having GMO soy in the US

Autism and Virus/Vaccines
This list is automatically updated

Dr. Cannell on Autism and Vitamin D in Vitamin D Life

• Autism treated by Vitamin D (80 – 120 ng) – Cannell update May 2018
• Autism Causes, Prevention and Treatment: Vitamin D Deficiency etc. – Book April 2015 Cannell
• Autism cured in a child with Vitamin D, Dr. Cannell comments and cofactor recommendations – March 2015
• Autism and Vitamin D - Dr. Cannell in Life Extension Mag - Jan 2014
• Autism treated by Vitamin D: Dr. Cannell - video June 2013
  • includes his list of 27 reasons to associate Vitamin D with Autism in 2013

Autism and Omega-3
This list is automatically updated

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Vitamin D Life - Overview Parkinson's and Vitamin D contains

• Vitamin D associated with Parkinson’s Disease in 55 studies, more studies needed- March 2022
• Parkinson's category has 112 studies
• Parkinson’s Disease and Vitamin D – review of 52 studies – May 2022
• Parkinson patients: 60 % taking Vitamin D – Dec 2019
• Low Vitamin D increases Parkinson's by 3X– July 2010 "only" a 30 year test, need more study
• Parkinson's disease prevented by Vitamin D, but small doses do not treat it - Aug 2023
• 10 clinical trials for PD with vitamin D intervention as of June 2023
• Parkinson’s Disease Summer School – alternative therapies included 60-80 ng of Vitamin D – Sept 2019
• Associated with PD are: Meta-analyses (12 ), Cognition (22 studies), Multiple Sclerosis (17 studies), VIRUS (4 studies), Omega-3 (3 studies), Vitamin D Receptor (11 studies)
• Note by the Founder of Vitamin D Life: I have twice recommended lots of Vitamin D to treat PD. Both got much better, but one had his doctor him cut back to just 2,000 IU. All of his recovery got reversed. With lots of vitamin D he could sing and bike, but now he can barely talk or walk

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104+ Vitamin D Life pages with BRAIN in the title

This list is automatically updated

• Perhaps drugs such as inhaled vitamin D can get directly to the brain – March 2018

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7+ Vitamin D Life pages with CNS in the title

This list is automatically updated

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Vitamin D Life - Variety of evidence that Vitamin D helps the brain – July 2014

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Study fails to mention that Vitamin D levels in cells can be much less than that in blood (gene problems)

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Vitamin D Life - Genetics category listing contains:

332 articles in the Genetics category

see also

• Vitamin D Receptor has 512 items
• Vitamin D Binding Protein = GC has 176 items
• CYP27B1 has 60 items
• CYP24A1 in title of 34+ items
• CYP2R1 25+ items
• Calcidiol has 46 items
• Calcitriol has 56 items
• Topical Vitamin D
• Nanoemulsion Vitamin D may be a substantially better form
• 1289 genes changed with higher doses of Vitamin D - RCT Dec 2019
• CYP3A4 (7 as of Dec 2022)
• Getting Vitamin D into your body
• 

Vitamin D blood test misses a lot

• Vitamin D from coming from tissues (vs blood) was speculated to be 50% in 2014, and by 2017 was speculated to be 90%
• Note: Good blood test results (> 40 ng) does not mean that a good amount of Vitamin D actually gets to cells
• A Vitamin D test in cells rather than blood was feasible (2017 personal communication)   Commercially available 2019
  • However, test results would vary in each tissue due to multiple genes
• Good clues that Vitamin D is being restricted from getting to the cells
  1) A vitamin D-related health problem runs in the family

    especially if it is one of 51+ diseases related to Vitamin D Receptor

+2) Slightly increasing Vitamin D shows benefits (even if conventional Vitamin D test shows an increase)+3) DNA and VDR tests - 120 to 200 dollars $100 to $250+4) PTH bottoms out ( shows that parathyroid cells are getting Vitamin d)

   Genes are good, have enough Magnesium, etc.

+4) Back Pain

   probably want at least 2 clues before taking adding vitamin D, Omega-3, Magnesium, Resveratrol, etc

• The founder of Vitamin D Life took action with clues #3&4

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