Developmental Vitamin D3 deficiency alters the adult rat brain

被引:212
作者
Féron, F
Burne, THJ
Brown, J
Smith, E
McGrath, JJ
Mackay-Sim, A
Eyles, DW [1 ]
机构
[1] Queensland Ctr Mental Hlth Res, Pk Ctr Mental Hlth, Wacol, Qld 4076, Australia
[2] Griffith Univ, Ctr Mol Neurobiol, Sch Biomol & Med Sci, Brisbane, Qld 4111, Australia
[3] Univ Queensland, Sch Biomed Sci, Brisbane, Qld 4072, Australia
[4] Univ Queensland, Dept Psychiat, Brisbane, Qld 4072, Australia
基金
英国医学研究理事会;
关键词
brain development; brain morphology; ventriculomegaly; NGF; schizophrenia;
D O I
10.1016/j.brainresbull.2004.12.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
There is growing evidence that Vitamin D-3 (1,25-dihydroxyvitamin D-3) is involved in brain development. We have recently shown that the brains of newborn rats from Vitamin D-3 deficient dams were larger than controls, had increased cell proliferation, larger lateral ventricles, and reduced cortical thickness. Brains from these animals also had reduced expression of nerve growth factor (NGF) and glial cell line-derived neurotrophic factor. The aim of the current study was to examine if there were any permanent outcomes into adulthood when the offspring of Vitamin D-3 deficient dams were restored to a normal diet. The brains of adult rats were examined at 10 weeks of age after Vitamin D-3 deficiency until birth or weaning. Compared to controls animals that were exposed to transient early Vitamin D-3 deficiency had larger lateral ventricles, reduced NGF protein content, and reduced expression of a number genes involved in neuronal structure, i.e. neurofilament or MAP-2 or neurotransmission, i.e. GABA-(alpha 4). We conclude that transient early life hypovitaminosis D-3 not only disrupts brain development but leads to persistent changes in the adult brain. In light of the high incidence of hypovitammosis D-3 in women of child-bearing age, the public health implications of these findings warrant attention. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:141 / 148
页数:8
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