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Endocrine Disrupting Effects of Triclosan on the Placenta in Pregnant Rats

机译:三氯生对孕鼠胎盘的内分泌干扰作用

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摘要

Triclosan (TCS) is a broad-spectrum antimicrobial agent that is frequently used in pharmaceuticals and personal care products. Reports have shown that TCS is a potential endocrine disruptor; however, the potential effects of TCS on placental endocrine function are unclear. The aim of this study was to investigate the endocrine disrupting effects of TCS on the placenta in pregnant rats. Pregnant rats from gestational day (GD) 6 to GD 20 were treated with 0, 30, 100, 300 and 600 mg/kg/d TCS followed by analysis of various biochemical parameters. Of the seven tissues examined, the greatest bioaccumulation of TCS was observed in the placenta. Reduction of gravid uterine weight and the occurrence of abortion were observed in the 600 mg/kg/d TCS-exposed group. Moreover, hormone detection demonstrated that the serum levels of progesterone (P), estradiol (E2), testosterone (T), human chorionic gonadotropin (hCG) and prolactin (PRL) were decreased in groups exposed to higher doses of TCS. Real-time quantitative reverse transcriptase-polymerase chain reaction (Q-RT-PCR) analysis revealed a significant increase in mRNA levels for placental steroid metabolism enzymes, including UDP-glucuronosyltransferase 1A1 (UGT1A1), estrogen sulfotransferase 1E1 (SULT1E1), steroid 5α-reductase 1 (SRD5A1) and steroid 5α-reductase 2 (SRD5A2). Furthermore, the transcriptional expression levels of progesterone receptor (PR), estrogen receptor (ERα) and androgen receptor (AR) were up-regulated. Taken together, these data demonstrated that the placenta was a target tissue of TCS and that TCS induced inhibition of circulating steroid hormone production might be related to the altered expression of hormone metabolism enzyme genes in the placenta. This hormone disruption might subsequently affect fetal development and growth.
机译:三氯生(TCS)是一种广谱抗菌剂,经常用于药物和个人护理产品中。报告显示,TCS是潜在的内分泌干扰物。但是,TCS对胎盘内分泌功能的潜在影响尚不清楚。这项研究的目的是研究TCS对妊娠大鼠胎盘的内分泌干扰作用。用0、30、100、300和600 mg / kg / d TCS处理妊娠第6天至GD 20的妊娠大鼠,然后分析各种生化参数。在检查的七个组织中,在胎盘中观察到最大的TCS生物蓄积。在暴露于600 mg / kg / d TCS的组中,观察到子宫重量的减轻和流产的发生。此外,激素检测表明,暴露于较高剂量TCS的组中,孕酮(P),雌二醇(E2),睾丸激素(T),人绒毛膜促性腺激素(hCG)和催乳激素(PRL)的血清水平降低。实时定量逆转录聚合酶链反应(Q-RT-PCR)分析显示胎盘类固醇代谢酶(包括UDP-葡萄糖醛酸转移酶1A1(UGT1A1),雌激素磺基转移酶1E1(SULT1E1),类固醇5α-还原酶1(SRD5A1)和类固醇5α-还原酶2(SRD5A2)。此外,孕激素受体(PR),雌激素受体(ERα)和雄激素受体(AR)的转录表达水平上调。综上所述,这些数据表明胎盘是TCS的靶组织,TCS诱导的循环类固醇激素产生的抑制作用可能与胎盘中激素代谢酶基因表达的改变有关。这种激素破坏可能随后影响胎儿的发育和生长。

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