Maternal obesity affects gene expression and cellular development in fetal brains.

Objectives: Female rat neonates reared on a high carbohydrate (HC) milk formula developed chronic hyperinsulinemia and adult-onset obesity (HC phenotype). Furthermore, we have shown that fetal development in the HC intrauterine environment (maternal obesity complicated with hyperinsulinemia, hyperle...

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Publicado en:Nutritional Neuroscience Vol. 16; no. 3; pp. 96 - 104
Autores principales: Stachowiak, Ewa K, Oommen, Saji, Vasu, Vihas T, Srinivasan, Malathi, Stachowiak, Michal, Gohil, Kishorchandra, Patel, Mulchand S
Formato: Journal Article
Publicado: Taylor & Francis Ltd Mar2013
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Mar2013
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      pub: Taylor & Francis Ltd
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        atl: Maternal obesity affects gene expression and cellular development in fetal brains.
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          Stachowiak, Ewa K
          Oommen, Saji
          Vasu, Vihas T
          Srinivasan, Malathi
          Stachowiak, Michal
          Gohil, Kishorchandra
          Patel, Mulchand S
        affil: Department of Pathology and Anatomic SciencesSchool of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, NY, USA
      sug:
      ab: Objectives: Female rat neonates reared on a high carbohydrate (HC) milk formula developed chronic hyperinsulinemia and adult-onset obesity (HC phenotype). Furthermore, we have shown that fetal development in the HC intrauterine environment (maternal obesity complicated with hyperinsulinemia, hyperleptinemia, and increased levels of proinflammatory markers) resulted in increased levels of serum insulin and leptin in term HC fetuses and the spontaneous transfer of the HC phenotype to the adult offspring. The objectives of this study are to identify changes in global gene expression pattern and cellular development in term HC fetal brains in response to growth in the adverse intrauterine environment of the obese HC female rat. Methods: GeneChip analysis was performed on total RNA obtained from fetal brains for global gene expression studies and immunohistochemical analysis was performed on fetal brain slices for investigation of cellular development in term HC fetal brains. Results: Gene expression profiling identified changes in several clusters of genes that could contribute to the transfer of the maternal phenotype (chronic hyperinsulinemia and adult-onset obesity) to the HC offspring. Immunohistochemical analysis indicated diminished proliferation and neuronal maturation of stem-like cells lining the third ventricle, hypothalamic region, and the cerebral cortex in HC fetal brains. Discussion: These results suggest that maternal obesity during pregnancy could alter the developmental program of specific fetal brain cell-networks. These defects could underlie pathologies such as metabolic syndrome and possibly some neurological disorders in the offspring at a later age.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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