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Title: Maternal exposure to low doses of DES altered mRNA expression of hepatic microsomal enzymes in male rat offspring. Author: Nishikawa O, Arishima K, Kobayashi T, Shirai M, Murakami M, Sakaue M, Yamamoto M. Journal: J Vet Med Sci; 2012 Feb; 74(2):247-53. PubMed ID: 21959891. Abstract: Our previous studies demonstrated that prenatal diethylstilbestrol (DES) treatment disrupts steroidogenesis but induces high-level expression of androgen receptor (AR) mRNA to inhibit the disruption of spermatogenesis. This study examined which prenatal DES treatment influenced hepatic microsomal enzymes, CYP3A1, CYP2B1/2, CYP2C11, UGT2B1 (UDP-glucuronosyltransferase 2B1), and IGF-1 (insulin-like growth factor-1), in male rat offspring. DES treatment decreased the mRNA expression levels of CYP3A1 and CYP2B1/2, but did not alter the expression of CYP2C11. At 6 weeks, DES treatment increasd the mRNA expression levels of UGT2B1 and IGF-1. These results suggest that prenatal DES treatment alters two hepatic enzymes (CYP3A1 and CYP2B1/2) and IGF-1 mRNA expression levels to counteract the low level of testosterone, but this disrupted UGT2B1 mRNA expression reduces the testosterone level.[Abstract] [Full Text] [Related] [New Search]