Vitamin D and the brain: Key questions for future research

被引:80
作者
Cui, Xiaoying [1 ]
Gooch, Helen [1 ]
Groves, Natalie J. [1 ]
Sah, Pankaj [1 ]
Burne, Thomas H. [1 ,2 ]
Eyles, Darryl W. [1 ,2 ]
McGrath, John J. [1 ,2 ,3 ]
机构
[1] Univ Queensland, Queensland Brain Inst, Brisbane, Qld 4072, Australia
[2] Queensland Ctr Mental Hlth Res, Wacol, Qld 4076, Australia
[3] Univ Queensland, Discipline Psychiat, Brisbane, Qld 4072, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
25?Hydroxyvitamin D; Neuroscience; Psychiatry; Schizophrenia; Calcium channels; D DEFICIENCY ALTERS; CALCIUM-CHANNEL; 1,25-DIHYDROXYVITAMIN D-3; MULTIPLE-SCLEROSIS; D-RECEPTOR; RAT; RISK; SCHIZOPHRENIA; EXPRESSION; RESPONSES;
D O I
10.1016/j.jsbmb.2014.11.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Over the last decade a convergent body of evidence has emerged from epidemiology, animal experiments and clinical trials which links low vitamin D status with a range of adverse neuropsychiatric outcomes. This research demonstrates that the timing of exposure to low vitamin D influences the nature of brain phenotypes, as exposures during gestation versus adulthood result in different phenotypes. With respect to early life exposures, there is robust evidence from rodent experiments indicating that transient developmental vitamin D (DVD) deficiency is associated with changes in brain structure, neurochemistry, gene and protein expression and behavior. In particular, DVD deficiency is associated with alterations in the dopaminergic neurotransmitter systems. In contrast, recently published animal experiments indicate that adult vitamin D (AVD) deficiency is associated with more subtle neurochemical and behavioral phenotypes. This paper explores key issues that need to be addressed in future research. There is a need to define the timing and duration of the 'critical window' during which low vitamin D status is associated with differential and adverse brain outcomes. We discuss the role for 'two-hit hypotheses', which propose that adult vitamin D deficiency leaves the brain more vulnerable to secondary adverse exposures, and thus may exacerbate disease progression. Finally, we explore the evidence implicating a role for vitamin D in rapid, non-genomic mechanisms that may involve L-type calcium channels and brain function. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:305 / 309
页数:5
相关论文
共 74 条
  • [1] L-type voltage-gated calcium channel blockade with isradipine as a therapeutic strategy for Alzheimer's disease
    Anekonda, Thimmappa S.
    Quinn, Joseph F.
    Harris, Christopher
    Frahler, Kate
    Wadsworth, Teri L.
    Woltjer, Randall L.
    [J]. NEUROBIOLOGY OF DISEASE, 2011, 41 (01) : 62 - 70
  • [2] Vitamin D deficiency and depression in adults: systematic review and meta-analysis
    Anglin, Rebecca E. S.
    Samaan, Zainab
    Walter, Stephen D.
    McDonald, Sarah D.
    [J]. BRITISH JOURNAL OF PSYCHIATRY, 2013, 202 (02) : 100 - 107
  • [3] Vitamin D and cognitive performance in adults: a systematic review
    Annweiler, C.
    Allali, G.
    Allain, P.
    Bridenbaugh, S.
    Schott, A. -M.
    Kressig, R. W.
    Beauchet, O.
    [J]. EUROPEAN JOURNAL OF NEUROLOGY, 2009, 16 (10) : 1083 - 1089
  • [4] Low Serum Vitamin D Concentrations in Alzheimer's Disease: A Systematic Review and Meta-Analysis
    Annweiler, Cedric
    Llewellyn, David J.
    Beauchet, Olivier
    [J]. JOURNAL OF ALZHEIMERS DISEASE, 2013, 33 (03) : 659 - 674
  • [5] Vitamin D Deficiency Exacerbates Experimental Stroke Injury and Dysregulates Ischemia-Induced Inflammation in Adult Rats
    Balden, Robyn
    Selvamani, Amutha
    Sohrabji, Farida
    [J]. ENDOCRINOLOGY, 2012, 153 (05) : 2420 - 2435
  • [6] Vitamin D, cognition, and dementia A systematic review and meta-analysis
    Balion, Cynthia
    Griffith, Lauren E.
    Strifler, Lisa
    Henderson, Matthew
    Patterson, Christopher
    Heckman, George
    Llewellyn, David J.
    Raina, Parminder
    [J]. NEUROLOGY, 2012, 79 (13) : 1397 - 1405
  • [7] Osteoblast Ca2+ permeability and voltage-sensitive Ca2+ channel expression is temporally regulated by 1,25-dihydroxyvitamin D3
    Bergh, JJ
    Shao, Y
    Puente, E
    Duncan, RL
    Farach-Carson, MC
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2006, 290 (03): : C822 - C831
  • [8] CACNA1C (Cav1.2) in the pathophysiology of psychiatric disease
    Bhat, Shambhu
    Dao, David T.
    Terrillion, Chantelle E.
    Arad, Michal
    Smith, Robert J.
    Soldatov, Nikolai M.
    Gould, Todd D.
    [J]. PROGRESS IN NEUROBIOLOGY, 2012, 99 (01) : 1 - 14
  • [9] Genetic Variation in CACNA1C Affects Brain Circuitries Related to Mental Illness
    Bigos, Kristin L.
    Mattay, Venkata S.
    Callicott, Joseph H.
    Straub, Richard E.
    Vakkalanka, Radhakrishna
    Kolachana, Bhaskar
    Hyde, Thomas M.
    Lipska, Barbara K.
    Kleinman, Joel E.
    Weinberger, Daniel R.
    [J]. ARCHIVES OF GENERAL PSYCHIATRY, 2010, 67 (09) : 939 - 945
  • [10] Vitamin D and cancer
    Bouillon, Roger
    Eelen, Guy
    Verlinden, Lieve
    Mathieu, Chantal
    Carmeliet, Geert
    Verstuyf, Annemieke
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2006, 102 (1-5) : 156 - 162