These authors contributed equally to this work.
Animal Proteomics
Developmental vitamin D deficiency alters brain protein expression in the adult rat: Implications for neuropsychiatric disorders
Article first published online: 13 FEB 2007
DOI: 10.1002/pmic.200600392
Copyright © 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Almeras, L., Eyles, D., Benech, P., Laffite, D., Villard, C., Patatian, A., Boucraut, J., Mackay-Sim, A., McGrath, J. and Féron, F. (2007), Developmental vitamin D deficiency alters brain protein expression in the adult rat: Implications for neuropsychiatric disorders. PROTEOMICS, 7: 769–780. doi: 10.1002/pmic.200600392
Publication History
- Issue published online: 5 MAR 2007
- Article first published online: 13 FEB 2007
- Manuscript Received: 26 MAY 2006
Funded by
- “Association pour la Recherche sur la Sclérose en Plaques” (ARSEP)
- Stanley Medical Research Institute
- National Health and Medical Research Council of Australia
- LFSEP/CNRS
Keywords:
- Mitochondria;
- Multiple sclerosis;
- Schizophrenia;
- Synapse;
- Vitamin D
Abstract
An increased risk for multiple sclerosis and schizophrenia is observed at increasing latitude and in patients born in winter or spring. To explore a possible link between maternal vitamin D deficiency and these brain disorders, we examined the impact of prenatal hypovitaminosis D on protein expression in the adult rat brain. Vitamin D-deficient female rats were mated with vitamin D normal males. Pregnant females were kept vitamin D-deficient until birth whereupon they were returned to a control diet. At week 10, protein expression in the progeny's prefrontal cortex and hippocampus was compared with control animals using silver staining 2-D gels associated with MS and newly devised data mining software. Developmental vitamin D (DVD) deficiency caused a dysregulation of 36 brain proteins involved in several biological pathways including oxidative phosphorylation, redox balance, cytoskeleton maintenance, calcium homeostasis, chaperoning, PTMs, synaptic plasticity and neurotransmission. A computational analysis of these data revealed that (i) nearly half of the molecules dysregulated in our animal model have also been shown to be misexpressed in either schizophrenia and/or multiple sclerosis and (ii) an impaired synaptic network may be a consequence of mitochondrial dysfunction.

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