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  • Title: Effects of primary exposure to environmental and natural estrogens on vitellogenin production in carp (Cyprinus carpio) hepatocytes.
    Author: Rankouhi TR, van Holsteijn I, Letcher R, Giesy JP, van Den Berg M.
    Journal: Toxicol Sci; 2002 May; 67(1):75-80. PubMed ID: 11961218.
    Abstract:
    Vitellogenin (vtg) is a precursor of the yolk proteins lipovitelline and phosvitin and is synthesized as a consequence of estrogen-dependent gene expression in female and male hepatocytes of egg-laying vertebrates. Freshly isolated carp hepatocytes of a genetically uniform strain of adult male carp (Cyprinus carpio) were used to investigate the effects of primary exposure to estrogenic compounds on the vitellogenic response to xenoestrogens. Isolated carp hepatocytes were first exposed (primary exposure) to 50 or 100 microM of either methoxychlor (MXCL) or bisphenol A (BPA), different concentrations of estrone (E1; 1 or 10 nM) or 17beta-estradiol (E2; 0.1 or 1 nM) for 2 days. Hepatocytes were exposed to xenoestrogens (secondary exposure) at both 2 and 5 days after isolation. Hepatocytes were cultured for a total period of 8 days. A competitive indirect ELISA was used to determine the level of vtg after 8 days. The concentration of chemicals used for the primary exposure induced vtg to a level that was less than 10% of the response elicited by E2 (1000 nM). A cytotoxic response, measured by MTT, was not observed after primary exposure to any of the xenoestrogens. After primary exposure to MXCL, vtg production in response to E2 was increased by 4-fold, and vitellogenesis in response to E1 treatment was doubled compared with vitellogenesis without pretreatment. No significant differences were observed between primary exposure to 50 and 100 microM MXCL. Primary exposure to 50 and 100 microM BPA increased the maximum vtg production in response to secondary E2 exposure by about 5- and 7-fold, respectively. Primary exposure to BPA (50 and 100 microM) followed by secondary exposure to E1 showed a 4- and 5-fold increase of the vtg synthesis in comparison to E1 exposure alone. Primary exposure to the endogenous estrogens had no significant influence on the vtg synthesis in response to secondary exposure to E1 or E2. Compared to hepatocytes exposed only to MXCL or BPA, primary exposure to E2 increased the vtg synthesis in hepatocytes induced by MXCL or BPA by almost a factor of 2. Primary exposure to E1 increased vitellogenesis after secondary exposure to MXCL only marginally. The present results indicate that weakly estrogenic environmental chemicals such as MXCL and BPA can increase the sensitivity of carp hepatocytes towards endogenous estrogens with respect to VTG synthesis.
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