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Protein Expression in the Nucleus Accumbens of Rats Exposed to Developmental Vitamin D Deficiency
INTRODUCTION: Developmental vitamin D (DVD) deficiency is a candidate risk factor for schizophrenia. Animal models have confirmed that DVD deficiency is associated with a range of altered genomic, proteomic, structural and behavioural outcomes in the rat. Because the nucleus accumbens has been impli...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2396486/ https://www.ncbi.nlm.nih.gov/pubmed/18545652 http://dx.doi.org/10.1371/journal.pone.0002383 |
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author | McGrath, John Iwazaki, Takeshi Eyles, Darryl Burne, Thomas Cui, Xiaoying Ko, Pauline Matsumoto, Izuru |
author_facet | McGrath, John Iwazaki, Takeshi Eyles, Darryl Burne, Thomas Cui, Xiaoying Ko, Pauline Matsumoto, Izuru |
author_sort | McGrath, John |
collection | PubMed |
description | INTRODUCTION: Developmental vitamin D (DVD) deficiency is a candidate risk factor for schizophrenia. Animal models have confirmed that DVD deficiency is associated with a range of altered genomic, proteomic, structural and behavioural outcomes in the rat. Because the nucleus accumbens has been implicated in neuropsychiatric disorders, in the current study we examined protein expression in this region in adult rats exposed to DVD deficiency METHODS: Female Sprague Dawley rats were maintained on a vitamin D deficient diet for 6 weeks, mated and allowed to give birth, after which a diet containing vitamin D was reintroduced. Male adult offspring (n = 8) were compared to control male (n = 8). 2-D gel electrophoresis-based proteomics and mass spectroscopy were used to investigate differential protein expression. RESULTS: There were 35 spots, mapped to 33 unique proteins, which were significantly different between the two groups. Of these, 22 were down-regulated and 13 up-regulated. The fold changes were uniformly small, with the largest FC being −1.67. Within the significantly different spots, three calcium binding proteins (calbindin1, calbindin2 and hippocalcin) were altered. Other proteins associated with DVD deficiency related to mitochondrial function, and the dynamin-like proteins. CONCLUSIONS: Developmental vitamin D deficiency was associated with subtle changes in protein expression in the nucleus accumbens. Disruptions in pathways related to calcium-binding proteins and mitochondrial function may underlie some of the behavioural features associated with animal models of developmental vitamin D deficiency |
format | Text |
id | pubmed-2396486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-23964862008-06-11 Protein Expression in the Nucleus Accumbens of Rats Exposed to Developmental Vitamin D Deficiency McGrath, John Iwazaki, Takeshi Eyles, Darryl Burne, Thomas Cui, Xiaoying Ko, Pauline Matsumoto, Izuru PLoS One Research Article INTRODUCTION: Developmental vitamin D (DVD) deficiency is a candidate risk factor for schizophrenia. Animal models have confirmed that DVD deficiency is associated with a range of altered genomic, proteomic, structural and behavioural outcomes in the rat. Because the nucleus accumbens has been implicated in neuropsychiatric disorders, in the current study we examined protein expression in this region in adult rats exposed to DVD deficiency METHODS: Female Sprague Dawley rats were maintained on a vitamin D deficient diet for 6 weeks, mated and allowed to give birth, after which a diet containing vitamin D was reintroduced. Male adult offspring (n = 8) were compared to control male (n = 8). 2-D gel electrophoresis-based proteomics and mass spectroscopy were used to investigate differential protein expression. RESULTS: There were 35 spots, mapped to 33 unique proteins, which were significantly different between the two groups. Of these, 22 were down-regulated and 13 up-regulated. The fold changes were uniformly small, with the largest FC being −1.67. Within the significantly different spots, three calcium binding proteins (calbindin1, calbindin2 and hippocalcin) were altered. Other proteins associated with DVD deficiency related to mitochondrial function, and the dynamin-like proteins. CONCLUSIONS: Developmental vitamin D deficiency was associated with subtle changes in protein expression in the nucleus accumbens. Disruptions in pathways related to calcium-binding proteins and mitochondrial function may underlie some of the behavioural features associated with animal models of developmental vitamin D deficiency Public Library of Science 2008-06-11 /pmc/articles/PMC2396486/ /pubmed/18545652 http://dx.doi.org/10.1371/journal.pone.0002383 Text en Mc Grath et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article McGrath, John Iwazaki, Takeshi Eyles, Darryl Burne, Thomas Cui, Xiaoying Ko, Pauline Matsumoto, Izuru Protein Expression in the Nucleus Accumbens of Rats Exposed to Developmental Vitamin D Deficiency |
title | Protein Expression in the Nucleus Accumbens of Rats Exposed to Developmental Vitamin D Deficiency |
title_full | Protein Expression in the Nucleus Accumbens of Rats Exposed to Developmental Vitamin D Deficiency |
title_fullStr | Protein Expression in the Nucleus Accumbens of Rats Exposed to Developmental Vitamin D Deficiency |
title_full_unstemmed | Protein Expression in the Nucleus Accumbens of Rats Exposed to Developmental Vitamin D Deficiency |
title_short | Protein Expression in the Nucleus Accumbens of Rats Exposed to Developmental Vitamin D Deficiency |
title_sort | protein expression in the nucleus accumbens of rats exposed to developmental vitamin d deficiency |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2396486/ https://www.ncbi.nlm.nih.gov/pubmed/18545652 http://dx.doi.org/10.1371/journal.pone.0002383 |
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