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Syst Biol Reprod Med. 2012 Feb;58(1):57-62. doi: 10.3109/19396368.2011.648820.

4-vinylcyclohexene diepoxide: a model chemical for ovotoxicity.

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  • 1Department of Physiology, College of Medicine, The University of Arizona, Tucson, AZ 85724, USA. hoyer@email.arizona.edu

Abstract

The occupational chemical 4-vinylcyclohexene diepoxide (VCD) has been shown to cause selective destruction of ovarian small pre-antral (primordial and primary) follicles in rats and mice by accelerating the natural, apoptotic process of atresia. Chemicals that destroy primordial follicles are of concern to women because exposure can result in premature ovarian failure (early menopause). Initial studies using in vivo exposure of rats determined that VCD specifically targets primordial and primary (small pre-antral) follicles and that repeated dosing is required. Through a method of isolation of ovarian small follicles, biochemical and molecular studies determined that intracellular pro-apoptotic pathways are activated following VCD dosing in rats. Subsequently an in vitro system using cultured whole neonatal rat ovaries was developed to provide more mechanistic information. That approach was used to demonstrate that the cell survival c-kit/kit ligand signaling pathway is the direct target for VCD-induced ovotoxicity. Specifically, VCD directly interacts with the oocyte-associated c-kit receptor to inhibit its autophosphorylation, and thereby impair oocyte viability. The cellular and molecular approach developed to determine these findings is described in this article.

PMID:
22239082
[PubMed - indexed for MEDLINE]
PMCID:
PMC3307534
Free PMC Article
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