Pharmacological Reports, 2013, 65, 271-278 ISSN 1734-1140
Matgorzata Wrzosek1, Jacek tukaszkiewicz2, Michat Wrzosek3, Andrzej Jakubczyk4, Halina Matsumoto4, Pawet Piatkiewicz3, Maria Radziwoh-Zaleska4, Marcin Wojnar4,5, Grazyna Nowicka1
department of Pharmacogenomics, department of Biochemistry and Clinical Chemistry,
department of Internal Medicine and Diabetology, department of Psychiatry, Medical University of Warsaw, Zwirki i Wigury 61, PL 02-091 Warszawa, Poland
department of Psychiatry, University of Michigan, 4250 Plymouth Rd., Ann Arbor, MI 48109, USA Correspondence: Grazyna Nowicka, e-mail: grazyna.nowicka at wum.edu.p
Vitamin D is formed in human epithelial cells via photochemical synthesis and is also acquired from dietary sources. The so-called classical effect of this vitamin involves the regulation of calcium homeostasis and bone metabolism. Apart from this, non-classical effects of vitamin D have recently gained renewed attention. One important yet little known of the numerous functions of vitamin D is the regulation of nervous system development and function. The neuroprotective effect of vitamin D is associated with its influence on neurotrophic production and release, neuromediator synthesis, intracellular calcium homeostasis, and prevention of oxidative damage to nervous tissue. Clinical studies suggest that vitamin D deficiency may lead to an increased risk of disease of the central nervous system (CNS), particularly schizophrenia and multiple sclerosis. Adequate intake of vitamin D during pregnancy and the neonatal period seems to be crucial in terms of prevention of these diseases.
Abbreviations: CNS - central nervous system, DBP - vitamin D binding protein, DVD - developmental vitamin D, GDNF -glial cell line-derived neurotrophic factor, iNOS - inducible nitric oxide synthase, MARRS receptor - membrane associated, rapid response steroid-binding receptor, NGF - nerve growth factor, SOCE - store-operated calcium entry, TH - tyrosine hydroxylase, 25(OH)D - 25-hydroxyvitamin D3
Table of contents
- Overview MS and vitamin D
- Alzheimers-Cognition - Overview
- Dementia associated with low vitamin D in two thirds of studies – systematic review May 2013
- Alzheimer’s and Parkinson’s diseases associated with low vitamin D – meta-analysis June 2013
- Vitamin D reduces Alzheimer’s disease in at least 11 ways – Jan 2013
- Overview Schizophrenia and Vitamin D
- Dementia 19X more likely if low vitamin D – Jan 2012
- 98 pcnt of genes that Vitamin D activates to reduce MS are also activated by Interferon -May 2013
PDF is attached at the bottom of this page
The discovery of the systemic role of vitamin D opened a new area of research on the role of this vitamin in the modulation of physiological and pathological processes, as well as the prevention and treatment of many diseases. While a number of reports exist describing the pleiotropic effects of vitamin D and its role in the development of cardiovascular disease, diabetes, and various cancers, less attention has been paid to the effects of vitamin D on the development and function of the nervous system. This paper seeks to highlight the neuroprotective and neurohormonal effects of this vitamin.
The major role of vitamin D in the human body is commonly related to calcium metabolism and bone structure, and vitamin D deficiency is associated with the development of rickets in children and osteoporosis in adults. However, scientific evidence clearly indicates that the biological importance of this vitamin greatly exceeds these aspects. Currently, there is no doubt that vitamin D is involved in a number of processes, that it constitutes an important factor in maintaining health, and that its deficiency is associated with the development of various pathological processes. Low levels of vitamin D are considered to be an important factor contributing to the development of cardiovascular diseases, metabolic syndrome and type 2 diabetes mellitus, inflammatory or immune disorders, as well as common cancers [8, 50, 64].
In humans, a natural source of vitamin D is its synthesis in the skin upon exposure to sunlight [ultraviolet B (UVB) radiation with a wavelength of 290-315 nm]. The level of exposure to sunlight determines the rate of synthesis of vitamin D in the skin. This depends on such environmental factors as geographic latitude, season, time of day, cloud coverage as well as personal characteristics, such as skin pigmentation, age, clothing, typical amount of time spent outdoors, and the use of anti-UV protection. Low exposure to sunlight is associated with a low rate of vitamin D biosynthesis. However, excessive exposure does not result in a further increase in synthesis of vitamin D due to its rapid photodegradation into a variety of biologically inactive photoproducts [29, 68]. Vitamin D is also obtained from the diet. The main dietary sources of cholecalciferol are fatty fish (such as eel, herring, salmon, mackerel), fish oil, and egg yolk, as well as margarines and other products fortified with vitamin D. The presence of vitamin D in foods other than these is limited.
A specific protein that binds vitamin D, vitamin D binding protein (DBP), transfers it through the circulatory system primarily to the liver, where the first step in the metabolic activation of vitamin D takes place. This involves the enzymatic hydroxylation of carbon 25. The resulting 25-hydroxyvitamin D (25(OH)D) is the main circulating metabolite of vitamin D, with a typical half life of 2 to 3 weeks. This is why the level of 25(OH)D is considered to be an indicator of vitamin D status in the body. Next, 25(OH)D is transported to the kidneys (and to some other tissues, e.g., the skin, and cells of the immune system), where calcitriol (1a,25-(OH)2D3) is formed via the enzyme 1a- hydroxylase (CYP27B1). This is a biologically active form of vitamin D , considered a hormone. Calcitriol molecules are transported to the cells of various organs, where they influence a number of biological processes by activating receptors for the active form of vitamin D. Moreover, some organs have the ability to produce locally the steroid hormone 1 a,25-(OH) D, which generates cell-specific actions, e.g., proliferation, differentiation or immune regulation .
An active metabolite of vitamin D, 1,25-dihydroxy-cholecalciferol, affects target cell function by regulating gene expression and via non-genomic action. In the former, an intracellular vitamin D receptor (VDR), belonging to the family of nuclear receptors, acts as a transcription factor, modifying the expression of a number of genes associated with various metabolic pathways . The other, non-genomic effect of 1,25-(OH) D involves membrane-associated rapid response steroid-binding (MARRS) receptors for vitamin D located in plasma membrane caveolae [38, 49]. Via these receptors, the hormonal form of vitamin D regulates cytosolic calcium concentration by releasing calcium (Ca ) ions from intracellular stores and the influx of calcium ions through calcium channels. It also affects the activity of phospholipase C (PLC), adenylate cyclase as well as Raf and MAP kinase pathways [18, 65]. Vitamin D receptors have been found in cells of various tissues, not only those directly responsible for calcium metabolism. These include pancreas ft cells, stomach cells, the ovaries, the testes, the thymus, white blood cell precursors, parathyroid tissue, and brain cells . These findings indicate an important role for these receptors, and for vitamin D itself, in regulating various metabolic processes, and underscore the vitamin's pleiotropic effects.
The vitamin D receptor gene (VDR) is located on the long arm of chromosome 12 (12q13.1), and has several polymorphisms, for example FokI, BsmI, Tru9I, EcoRV, ApaI, TaqI, and Cdx2, which might have biological effects resulting in susceptibility to different diseases. Currently, data are available describing an association between VDR gene variants and risk of diabetes, cancer (cancer of the prostate, colon), osteoporosis, autoimmune disorders (lupus, cirrhosis, hepatitis, Crohn's disease, Graves' disease), and kidney diseases [62, 63]. Specific VDR polymorphisms have also been considered as possible risk factors for developing schizophrenia as well as multiple sclerosis, but this relation still awaits confirmation [26, 33, 42].
There is evidence indicating the role of vitamin D in regulating the development and function of nerve cells and the potential ramifications of vitamin D deficiency in this respect.
The involvement of vitamin D in the function of the central nervous system is supported by the presence of the enzyme 25(OH)D3-1a-hydroxylase, responsible for the formation of the active form of vitamin D, as well as the presence of vitamin D receptors in the brain, mainly in the hypothalamus and dopa-minergic neurons of the substantia nigra . Vitamin D is believed to play a similar role to that of neu-rosteroids. Due to its interaction with the MARRS receptors, the hormonal form of vitamin D affects various intracellular metabolic pathways [38, 49]. Moreover, the enzyme 1 a-hydroxylase and the nuclear VDRs are also present in the microglia, i.e., non-neuronal cells of the central nervous system (CNS). This suggests both autocrine and paracrine effects for calcitriol on nerve cells .
The influence of the active form of vitamin D on the nervous system is associated with modifying the production and release of neurotrophic factors such as nerve growth factor (NGF), which is essential for neuron differentiation, as well as increasing the levels of glial cell line-derived neurotrophic factor (GDNF). In addition, vitamin D has been shown to significantly increase the rate of neurite outgrowth when added to hippocampal explants . Moreover, 1,25-(OH)2 D3 is an important factor modifying the synthesis of such neuromediators as acetylcholine via increased gene expression ofthe enzyme choline acetyltransferase (CAT) [24, 60]. Vitamin D has also been found to affect the expression of genes associated with GABA-ergic neu-rotransmission  and to stimulate the expression of tyrosine hydroxylase (TH), responsible for catecholamine biosynthesis [52, 56].
The neuroprotective role of vitamin D involves the synthesis of proteins binding calcium (Ca ) ions (e.g., parvoalbumin) and thus maintaining cellular calcium homeostasis, which is very important for brain cell function [9, 20, 61]. Moreover, 1,25-(OH) D administration was shown to down-regulate L-type voltage-sensitive Ca channel expression in rat hippocampal cultures. This indicates the protective effect of the hormonal form of vitamin D on the brain via a reduction in the influx of calcium ions into neurons . It has also been shown, based on studies on immature rats, that vitamin D modulates L-type calcium channel opening via nongenomic effects through various kinase pathways and enzyme activities in the cerebral cortex . It is worth emphasizing that maintaining the appropriate level of calcium ions in nerve cells is especially important for their normal function. Physiologically, an increase in calcium (Ca ) ions in nerve cells contributes to an increased release of glutamic and asparaginic acids that stimulate the N-methyl-D-aspartate (NMDA) receptors to open the calcium channels, which results in nerve cell depolarization and increased influx of Ca ions through the voltage-dependent calcium channels. Increased levels of these ions in cytosol lead to the fusion of synaptic vesicles with the presynaptic membrane and the release of transmitters. Excess calcium in nerve cells can contribute to excitotoxicity because it leads to an increased release of stimulating amino acids and other neurotransmitters, the activation of nitric oxide synthase (NOS), and the formation of reactive oxygen species (ROS), as well as the activation of proteases and lipases, leading to plasmic and mitochondrial membrane damage. A disruption in calcium ion transport and high calcium levels triggers the arachidonic acid cascade and enhances lipid peroxidation .
Vitamin D also stimulates the influx of Ca ions through store-operated calcium entry (SOCE) channels, located in cells such as skeletal muscle cells or lymphocytes. This involves stromal interaction molecule (STIM) proteins that play the role of calcium level sensors in these cells and regulate the SOCE process [40, 65]. Recently published data by Grusz-czynska-Biegala et al.  indicate that neurons replenish their internal calcium stores with this mechanism. It has not been established yet whether vitamin D's involvement in the regulation of these recently discovered paths of calcium influx extends to the nerve cells.
Rat neuron culture studies showed that 1,25-(OH) D increases glutathione levels in these cells. The reduced form of glutathione (GSH), supplied into nerve cells by astrocytes, is a fundamental antioxidant protecting cells against ROS and apoptosis caused by oxidation. This suggests an important neuroprotective effect for the active form of vitamin D , by counteracting oxidative damage to the CNS [27, 58]. In addition, vitamin D inhibits the synthesis of inducible nitric oxide synthase (iNOS). In a hypoxic environment, this enzyme becomes activated in neurons, which yields a substantial amount of nitric oxide (NO), high levels of which initiate a cascade of neurotoxicity and neuron death. This is due to the fact that NO is a precursor of peroxynitrite ONOO , which in turn leads to the deactivation of a series of enzymes by reacting, for example, with sulfhydryl (-SH) groups as well as by injuring mitochondria and disturbing cellular energy processes [51, 54]. As an iNOS inhibitor, vitamin D protects the brain from peroxynitrite-mediated neuronal damage. Limiting this enzyme's activity may play a role in nerve tissue protection from such neurodegenerative conditions as Parkinson's, Alzheimer's, or Huntington's disease .
The results of many studies suggest an impact of vitamin D on immune system function as well as on the development of inflammation. Suppressive effects of calcitriol on interferon y (IF-y) or interleukin-2 (IL-2) production by stimulating the synthesis of interleukin-10 (IL-10), also known as the cytokine synthesis inhibitory factor (CSIF), have been demonstrated [1, 13, 50]. Additionally, administration of 1,25(OH) D was shown to inhibit the production of tumor necrosis factor-a, interleukin-6, and NO in the EOC13 microglial cell line, indicating direct anti-inflammatory properties for calcitriol on microglia . At the same time, depression and autoimmune diseases, including multiple sclerosis, are believed to be associated with overproduction ofpro-inflammatory cytokines that disrupt normal brain cell metabolism. Thus, vitamin D, with its immunomodulating effects, may decrease the risk of these processes .
There has been growing interest in the potential effect of calcitriol on human glioma cells. Induction of steroidogenic genes by vitamin D was observed in human GI-1 cells . In glioblastoma multiforme (GBM) cell lines (Tx3095, Tx3868, U87, U118,
U373), no influence of vitamin D on cell growth regulation was found indicating resistance of these cells against antiproliferative effect of calcitriol . However, multidirectional action of calcitriol in glio-blastoma multiforme, depending on cell environment, and possibly depending on the various molecular profiles involved in metabolizing vitamin D , was suggested . Therefore, the potential role of vitamin D in human glioma therapeutical concept is still under discussion.
Animal studies have shown that vitamin D deficiency may increase the risk of brain dysfunction. It was reported that vitamin D deficiency significantly affects brain cell differentiation and proliferation during the neonatal period. The timing of correction of vitamin D intake and levels was found to influence persistence of some of these changes and animal behavior [for review see 16]. At this point, it is worth mentioning the studies by Harms et al.  conducted on rat dams fed a diet depleted in vitamin D and exposed to no UVB radiation for 6 weeks prior to conception, and then throughout the entire pregnancy. Ten weeks after birth and already receiving a diet enriched with vitamin D, the young rats underwent a series of behavioral tests that measured social behaviors, anxiety levels, behavior during a forced swimming test, and motor activity. In comparison to control animals, those deprived of vitamin D during the prenatal period were shown to exhibit a more pronounced hyperlocomotor behavior after being introduced to a new environment. The symptoms observed in these animals are consistent with animal models of schizophrenia. This is supported by a positive response to antipsychotic drugs (haloperidol) in enhanced locomotor activity induced by developmental vitamin D (DVD) depletion, as demonstrated by Kesby et al. . In a similar study, conducted by Fernandes de Abreu et al. , the offspring of dams fed a diet deficient in vitamin D underwent an olfactory learning test. In comparison to control animals, the mice with DVD deficiency exhibited learning disability at week 30 after birth. Moreover, magnetic resonance imaging scans revealed that the cerebral lateral ventricles were reduced in size (which is, in fact, inconsistent with reports of an increased lateral ventricular volume in patients with schizophrenia). Furthermore, a significant loss in hippocampal volume in DVD-deficient mice was observed as late as at week 70 after birth. This confirms the hypothesis that the effect of vitamin D on brain function takes place mainly at the molecular, rather than cellular, level. The authors suggest that the learning disability found in the tested animals may be a result of vitamin D deficiency altering the expression of factors involved in neurotransmission and syn-aptic plasticity.
In 1999, McGrath stipulated that low prenatal vitamin D (especially during the third trimester) may be a risk factor for development of schizophrenia in offspring . This assumption was based on the fact that the majority of people who develop this condition were born in winter or spring, i.e., in the period when there is typically insufficient sun exposure to induce vitamin D synthesis in the skin. Among those suffering from schizophrenia, a relatively large proportion is made up of people of dark complexion who have migrated to regions of high latitude, as well as people who live in great metropolises, where the duration of sun exposure and outdoor activity are limited by lifestyle [27, 47]. Studies in African Americans showed a relationship between low levels of vitamin D in mothers during the third trimester of pregnancy and an increased risk of schizophrenia in their children . Similarly, a lack of vitamin D supplementation during the first year of life in Finnish boys correlated with an increased risk of developing schizophrenia . However, both low and high concentrations of neonatal vitamin D in Danish studies were associated with an increased risk of schizophrenia .
Apart from risk of schizophrenia, there is evidence, coming from human studies, linking vitamin D deficiency to increased risk of developing major depression . The US NHANES III study, conducted in 7,970 subjects aged 15 through 39, showed that the risk of depression was higher in those with low vitamin D levels . Moreover, in studies by May et al.  involving 7,358 subjects with cardiovascular disease (coronary artery disease, myocardial infarction, congestive heart failure, stroke, atrial fibrillation, or peripheral vascular disease), low levels of vitamin D were associated with episodes of depression. In a similar study, conducted in a group of elderly subjects (65-95 years old), the severity of depression also correlated with low serum 25(OH)D levels .
Clinical studies indicate a possible association of vitamin D deficiency with the development of Alzheimer's and Parkinson's diseases [12, 14, 20, 61]. In addition, poor vitamin D status has been implicated in the pathogenesis of dementias [5, 19]. It has been shown that 25(OH)D insufficiency (< 20 ng/ml) was associated with a higher risk of all-cause dementia (AD, stroke with dementia, and other) . Recently, it has been demonstrated that vitamin D modulates progesterone protection of the brain from traumatic injury. The protective effect of progesterone was reduced in vitamin D deficient animals, and combined vitamin D and progesterone therapy, more effectively than progesterone alone, increased the extent to which spatial and reference memory were safeguarded following bilateral contusions of the medial frontal cortex . These findings correspond to data reporting that vitamin D induces progesterone synthesis and progesterone-responsive gene expression in cell cultures . This and other lines of evidence suggest that vitamin D treatment might be critically important for preserving neurocognitive functions among the elderly. However, this hypothesis is still under discussion and need to be confirmed by larger studies.
Moreover, a small pilot study investigating vitamin D deficiency and seizure control in epilepsy found that administration of vitamin D in patients with pharmacoresistant epilepsy, and with low (< 30 ng/ml) serum 25(OH)D level, resulted in a median seizure number reduction of 40% . Animal studies also support an anticonvulsant effect for vitamin D, as administration of cholecalciferol enhances the anticonvulsant effect of conventional antiepileptic drugs , and increased seizure severity was present in vitamin D receptor knockout mice .
Adequate vitamin D supply may also lower the risk of multiple sclerosis (MS). This chronic demyelinating disease of the central nervous system leads to multifocal nervous tissue damage (axonal demyelination and disintegration) that may lead to spasticity and motor weakness. Seasonal vitamin D deficiency was observed to lead to symptom exacerbation . On the other hand, it was found that physical activity secondary to outdoor exercise and sunlight exposure in patients with relapsing-remitting MS was positively correlated with 25(OH)D serum levels which were higher than in inactive MS patients . In addition, patients with established MS and lower vitamin D levels are at higher risk for subsequent relapse [7, 48]. The influence of high treatment doses of vitamin D on MS patients was also studied. Twelve patients in an active phase of multiple sclerosis were given progressively increasing doses of vitamin D3: from 700 to 7,000 |ig/week (from 28,000 to 280,000 IU/week) along with 1,200 mg elemental Ca/day . After 28-weeks of treatment, the number of gadolinium-enhancing lesions per patient (assessed with a nuclear magnetic resonance brain scan) was found to decrease significantly. It has been postulated that the neuroprotective effects of vitamin D and its impact on the immune system may inhibit processes that lead to CNS damage, or act indirectly by activating restorative processes .
Adequate vitamin D status may play a very important role in terms of appropriate brain development and function [15, 22]. Therefore, adequate supply of vitamin D in specific periods of life, including the prenatal period, seems to be of particular importance, because it may reduce the risk of CNS diseases whose treatment is difficult and which represent a heavy burden both for the affected individuals and their society . What becomes particularly important in light of these reports is continued study of the effects of vitamin D on CNS function aimed at establishing a recommendation of vitamin D dietary intake, which is a key element in averting its deficiency, and making tests determining serum 25(OH)D concentration [34, 55] generally available.
This work was supported by the Polish Ministry of Science and Higher Education (MNiSW) grant No. NN 405 357 239.
- 1. Bartels LE, J0rgensen SP, Agnholt J, Kelsen J, Hvas CL, Dahlerup JF: 1,25-Dihydroxyvitamin D3 and dex-amethasone increase interleukin-10 production in CD4+ T cells from patients with Crohn's disease. Int Immuno-pharmacol, 2007, 7, 1755-1764.
- 2. Borowicz KK, Morawska M, Furmanek-Karwowska K, Luszczki JJ, Czuczwar SJ: Cholecalciferol enhances the anticonvulsant effect of conventional antiepileptic drugs in the mouse model of maximal electroshock. Eur J Pharmacol, 2007, 573, 111-115.
- 3. Brewer LD, Thibault V, Chen KC, Langub MC, Land-field PW, Porter NM: Vitamin D hormone confers neuro-protection in parallel with downregulation of L-type calcium channel expression in hippocampal neurons. J Neu-rosci, 2001, 21, 98-108.
- 4. Brown J, Bianco JI, McGrath JJ, Eyles DW: 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.
- 5. Buell JS, Dawson-Hughes B, Scott TM, Weiner DE, Dallal GE, Qui WQ, Bergethon P et al.: 25-Hydroxyvitamin D, dementia, and cerebrovascular pathology in elders receiving home services. Neurology, 2010, 74, 18-26.
- 6. Chaudhuri A: Why we should offer routine vitamin D supplementation in pregnancy and childhood to prevent multiple sclerosis. Med Hypotheses, 2005, 64, 608-618.
- 7. Correale J, Ysrraelit MC, Gaitan MI: Immunomodula-tory effects of vitamin D in multiple sclerosis. Brain, 2009, 132, 1146-1160.
- 8. De Luca HF: Overview of general physiologic features and functions of vitamin D. Am J Clin Nutr, 2004, 80, 1689-1696.
- 9. de Viragh PA, Haglid KG, Celio MR: Parvalbumin increases in the caudate putamen of rats with vitamin D hypervitaminosis. Proc Natl Acad Sci USA, 1989, 86, 3887-3890.
- 10. Diesel B, Radermacher J, Bureik M, Bernhardt R, Seifert M, Reichrath J, Fischer U, Meese E: Vitamin D3 metabolism in human glioblastoma multiforme: functionality of CYP27B1 splice variants, metabolism of calcidiol, and effect of calcitriol. Clin Cancer Res, 2005, 11, 5370-5380.
- 11. Dong XX, Wang Y, Qin ZH: Molecular mechanisms of excitotoxicity and their relevance to pathogenesis of neu-rodegenerative diseases. Acta Pharmacol Sin, 2009, 30, 379-387.
- 12. Dursun E, Gezen-Ak D, Yilmazer S: A novel perspective for Alzheimer's disease: Vitamin D receptor suppression by amyloid-P and preventing the amyloid-P induced alterations by vitamin D in cortical neurons. J Alzheimers Dis, 2011, 23, 207-219.
- 13. Dusso AS, Brown AJ, Slatopolsky E: Vitamin D. Am J Physiol Renal Physiol, 2005, 289, F8-28.
- 14. Evatt ML, Delong MR, Khazai N, Rosen A, Triche S, Tangpricha V: Prevalence of vitamin D insufficiency in patients with Parkinson disease and Alzheimer disease. Arch Neurol, 2008, 65, 1348-1352.
- 15. Eyles D, Burne T, McGrath J: Vitamin D in fetal brain development. Semin Cell Dev Biol, 2011, 22, 629-636.
- 16. Eyles DW, Burne TH, McGrath JJ: 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.
- 17. Eyles DW, Smith S, Kinobe R, Hewison M, McGrath JJ: Distribution of the vitamin D receptor and 1 a-hydroxylase in human brain. J Chem Neuroanat, 2005, 29, 21-30.
- 18. Falkenstein E, Tillmann HC, Christ M, Feuring M, Wehling M: Multiple actions of steroid hormones – a focus on rapid, nongenomic effects. Pharmacol Rev, 2000, 52, 513-556.
- 19. Farid K, Volpe-Gillot L, Petras S, Plou C, Caillat-Vigneron N, Blacher J: Correlation between serum 25-hydroxyvitamin D concentrations and regional cerebral blood flow in degenerative dementia. Nucl Med Commun, 2012, 33, 1048-1052.
- 20. Fernandes de Abreu DA, Eyles D, Feron F: Vitamin D, a neuro-immunomodulator: implications for neurodegenerative and autoimmune diseases. Psychoneuroendocrinology, 2009, 34, 265-277.
- 21. Fernandes de Abreu DA, Nivet E, Baril N, Khrestcha-tisky M, Roman F, Feron F: Developmental vitamin D deficiency alters learning in C57Bl/6J mice. Behav Brain Res, 2010, 208, 603-608.
- 22. Feron F, Burne TH, Brown J, Smith E, McGrath JJ, Mackay-Sim A, Eyles DW: Developmental vitamin D3 deficiency alters the adult rat brain. Brain Res Bull, 2005, 65, 141-148.
- 23. Ganji V, Milone C, Cody MM, McCarty F, Wang YT: Serum vitamin D concentrations are related to depression in young adult US population: the Third National Health and Nutrition Examination Survey. Int Arch Med, 2010, 11, 3-29.
- 24. Garcion E, Wion-Barbot N, Montero-Menei CN, Berger F, Wion D: New clues about vitamin D functions in the nervous system. Trends Endocrinol Metab, 2002, 13, 100-105.
- 25. Gruszczynska-Biegala J, Pomorski P, Wisniewska MB, Kuznicki J: Differential roles for STIM1 and STIM2 in store-operated calcium entry in rat neurons. PLoS One, 2011, 6, e19285.
- 26. Handoko HY, Nancarrow DJ, Mowry BJ, McGrath JJ: Polymorphisms in the vitamin D receptor and their associations with risk of schizophrenia and selected anthro-pometric measures. Am J Hum Biol, 2006, 18, 415-417.
- 27. Harms LR, Burne TH, Eyles DW, McGrath JJ: Vitamin D and the brain. Best Pract Res Clin Endocrinol Metab, 2011, 25, 657-669.
- 28. Harms LR, Eyles DW, McGrath JJ, Mackay-Sim A, Burne TH: Developmental vitamin D deficiency alters adult behaviour in 129/SvJ and C57BL/6J mice. Behav Brain Res, 2008, 187, 343-350.
- 29. Holick MF: The vitamin D epidemic and its health consequences. J Nutr, 2005, 135, 2739S-2748S.
- 30. Hollo A, Clemens Z, Kamondi A, Lakatos P, Szucs A: Correction of vitamin D deficiency improves seizure control in epilepsy: a pilot study. Epilepsy Behav, 2012, 24, 131-133.
- 31. Hoogendijk WJ, Lips P, Dik MG, Deeg DJ, Beekman AT, Penninx BW: Depression is associated with decreased 25-hydroxyvitamin D and increased parathyroid hormone levels in older adults. Arch Gen Psychiatry, 2008, 65, 508-512.
- 32. Hua F, Reiss JI, Tang H, Wang J, Fowler X, Sayeed I, Stein DG: Progesterone and low-dose vitamin D hormone treatment enhances sparing of memory following traumatic brain injury. Horm Behav, 2012, 61, 642-651.
- 33. Huang J, Xie ZF: Polymorphisms in the vitamin D receptor gene and multiple sclerosis risk: a meta-analysis of case-control studies. J Neurol Sci, 2012, 313, 79-85.
- 34. Huh SY, Gordon CM: Vitamin D deficiency in children and adolescents: epidemiology, impact and treatment. Rev Endocr Metab Disord, 2008, 9, 161-170.
- 35. Jamilian H, Bagherzadeh K, Nazeri Z, Hassanijirdehi M: Vitamin D, parathyroid hormone, serum calcium and phosphorus in patients with schizophrenia and major depression. Int J Psychiatry Clin Pract, 2013, 17, 30-34.
- 36. Kalueff AV, Minasyan A, Keisala T, Kuuslahti M, Mietti-nen S, Tuohimaa P: Increased severity of chemically induced seizures in mice with partially deleted vitamin D receptor gene. Neurosci Lett, 2006, 394, 69-73.
- 37. Kesby JP, Burne TH, McGrath JJ, Eyles DW: Developmental vitamin D deficiency alters MK 801-induced hy-perlocomotion in the adult rat: an animal model of schizophrenia. Biol Psychiatry, 2006, 60, 591-596.
- 38. Khanal RC, Peters TM, Smith NM, Nemere I: Membrane receptor-initiated signaling in 1,25(OH)2D3-stim-ulated calcium uptake in intestinal epithelial cells. J Cell Biochem, 2008, 105, 1109-1116.
- 39. Kimball SM, Ursell MR, O'Connor P, Vieth R: Safety of vitamin D3 in adults with multiple sclerosis. Am J Clin
- Nutr, 2007, 86, 645-651.
- 40. Kiviluoto S, Decuypere JP, De Smedt H, Missiaen L, Parys JB, Bultynck G: STIM1 as a key regulator for Ca2+ homeostasis in skeletal-muscle development and function. Skelet Muscle, 2011, 4, 1-16.
- 41. Lefebvre d'Hellencourt C, Montero-Menei CN, Bernard R, Couez D : Vitamin D3 inhibits proinflammatory cyto-kines and nitric oxide production by the EOC13 micro-glial cell line. J Neurosci Res, 2003, 71, 575-582.
- 42. Mackay-Sim A, Feron F, Eyles D, Burne T, McGrath J: Schizophrenia, vitamin D, and brain development. Int Rev Neurobiol, 2004, 59, 351-380.
- 43. May HT, Bair TL, Lappe DL, Anderson JL, Horne BD, Carlquist JF, Muhlestein JB: Association of vitamin D levels with incident depression among a general cardiovascular population. Am Heart J, 2010, 159, 1037-1043.
- 44. McGrath J: Hypothesis: is low prenatal vitamin D a risk-modifying factor for schizophrenia? Schizophr Res, 1999, 40, 173-177.
- 45. McGrath J, Eyles D, Mowry B, Yolken R, Buka S: Low maternal vitamin D as a risk factor for schizophrenia: a pilot study using banked sera. Schizophr Res, 2003, 63, 73-78.
- 46. McGrath JJ, Eyles DW, Pedersen CB, Anderson C, Ko P, Burne TH, Norgaard-Pedersen B et al.: Neonatal vitamin D status and risk oof schizophrenia: a population-based case-control study. Arch Gen Psychiatry, 2010, 67, 889-894.
- 47. McGrath J, Saari K, Hakko H, Jokelainen J, Jones P, Jarvelin MR, Chant D, Isohanni M: Vitamin D supplementation during the first year of life and risk of schizophrenia: a Finnish birth cohort study. Schizophr Res, 2004, 67, 237-245.
- 48. Mowry EM. Vitamin D: evidence for its role as a prognostic factor in multiple sclerosis. J Neurol Sci, 2011, 311, 19-22.
- 49. Nemere I, Garbi N, Hammerling GJ, Khanal RC: Intestinal cell calcium uptake and the targeted knockout of the 1,25D3-MARRS (membrane-associated, rapid response steroid-binding) receptor/PDIA3/Erp57. J Biol Chem, 2010, 285, 31859-31866.
- 50. Norman AW: From vitamin D to hormone D: fundamentals of the vitamin D endocrine system essential for good health. Review. Am J Clin Nutr, 2008, 88, 491S-499S.
- 51. Pannu R, Singh I: Pharmacological strategies for the regulation of inducible nitric oxide synthase: neurode-generative versus neuroprotective mechanisms. Neuro-chem Int, 2006, 49, 170-182.
- 52. Puchacz E, Stumpf WE, Stachowiak EK, Stachowiak MK: Vitamin D increases expression of the tyrosine hy-droxylase gene in adrenal medullary cells. Brain Res Mol Brain Res, 1996, 36, 193-196.
- 53. Reichrath S, Miiller CS, Gleissner B, Pfreundschuh M, Vogt T, Reichrath J: Notch- and vitamin D signaling in 1,25(OH)2D3-resistant glioblastoma multiforme (GBM) cell lines. J Steroid Biochem Mol Biol, 2010, 121, 420-424.
- 54. Robin E, Derichard A, Vallet B, Hassoun SM, Neviere R: Nitric oxide scavenging modulates mitochondrial dysfunction induced by hypoxia/reoxygenation. Pharmacol Rep, 2011, 63, 1189-1194.
- 55. Rovner AJ, O'Brien KO: Hypovitaminosis D among healthy children in the United States: a review of the current evidence. Arch Pediatr Adolesc Med, 2008, 162, 513-519.
- 56. Sanchez B, Relova JL, Gallego R, Ben-Batalla I, Perez-Fernandez R: 1,25-Dihydroxyvitamin D3 administration to 6-hydroxydopamine-lesioned rats increases glial cell line-derived neurotrophic factor and partially restores ty-rosine hydroxylase expression in substantia nigra and striatum. J Neurosci Res, 2009, 87, 723-732.
- 57. Schuster I: Cytochromes P450 are essential players in the vitamin D signaling system. Biochim Biophys Acta, 2011, 1814, 186-199.
- 58. Shinpo K, Kikuchi S, Sasaki H, Moriwaka F, Tashiro K: Effect of 1,25-dihydroxyvitamin D3 on cultured mesen-cephalic dopaminergic neurons to the combined toxicity caused by L-buthionine sulfoximine and 1-methyl-4-phenylpyridine. J Neurosci Res, 2000, 62, 374-382.
- 59. Smolders J, Damoiseaux J, Menheere P, Hupperts R: Vitamin D as an immune modulator in multiple sclerosis, a review. J Neuroimmunol, 2008, 194, 7-17.
- 60. Sonnenberg J, Luine VN, Krey LC, Christakos S: 1,25-Dihydroxyvitamin D3 treatment results in increased cho-line acetyltransferase activity in specific brain nuclei. Endocrinology, 1986, 118, 1433-1439.
- 61. Tuohimaa P, Keisala T, Minasyan A, Cachat J, Kalueff A: Vitamin D, nervous system and aging. Psychoneuro-endocrinology, 2009, 34, Suppl 1, 278-286.
- 62. Uitterlinden AG, Fang Y, Van Meurs JB, Pols HA, Van Leeuwen JP: Genetics and biology of vitamin D receptor polymorphisms. Gene, 2004, 338, 143-56.
- 63. Valdivielso JM, Fernandez E: Vitamin D receptor polymorphisms and diseases. Clin Chim Acta, 2006, 371, 1-12.
- 64. Van der Schueren BJ, Verstuyf A, Mathieu C: Straight from D-Heart: vitamin D status and cardiovascular disease. Curr Opin Lipidol, 2012, 23, 17-23.
- 65. Vazquez G, de Boland AR, Boland RL: 1a,25-Dihy-droxy-vitamin-D3-induced store-operated Ca2+ influx in skeletal muscle cells. Modulation by phospholipase C, protein kinase C, and tyrosine kinases. J Biol Chem, 1998, 273, 33954-33960.
- 66. Wang TT, Tavera-Mendoza LE, Laperriere D, Libby E, MacLeod NB, Nagai Y, Bourdeau V et al.: Large-scale in silieo and microarray-based identification of direct 1,25-dihydroxyvitamin D3 target genes. Mol Endocrinol, 2005, 19, 2685-2695.
- 67. Waschbisch A, Wenny I, Tallner A, Schwab S, Pfeifer K, Maurer M: Physical activity in multiple sclerosis: a comparative study of vitamin D, brain-derived neurotrophic factor and regulatory T cell populations. Eur Neurol, 2012, 68, 122-128.
- 68. Webb AR: Who, what, where and when - influences on cutaneous vitamin D synthesis. Prog Biophys Mol Biol, 2006, 92, 17-25.
- 69. Yagishita T, Kushida A, Tamura H: Vitamin D3 enhances all-trans retinoic acid (ATRA)-mediated neurosteroid biosynthesis in human glioma GI-1 cells. J Biochem 2012, 152, 285-292.
- 70. Zanatta L, Goulart PB, Goncalves R, Pierozan P, Winkelmann-Duarte EC, Woehl VM, Pessoa-Pureur R et al.: 1 a,25-Dihydroxyvitamin D3 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.