GNRHR公司
全氟辛烷
受体
内科学
内分泌学
雄激素受体
促黄体激素
激素受体
激素
生物
下丘脑-垂体-性腺轴
促卵泡激素
化学
促性腺激素释放激素
医学
磺酸盐
癌症
有机化学
乳腺癌
钠
前列腺癌
作者
S. López-Doval,R. Salgado,A. Lafuente
出处
期刊:Chemosphere
[Elsevier]
日期:2016-05-02
卷期号:155: 488-497
被引量:28
标识
DOI:10.1016/j.chemosphere.2016.04.081
摘要
This study was undertaken to evaluate the possible role of several reproductive hormone receptors on the disruption of the hypothalamic-pituitary-testis (HPT) axis activity induced by perfluorooctane sulfonate (PFOS). The studied receptors are the gonadotropin-releasing hormone receptor (GnRHr), luteinizing hormone receptor (LHr), follicle-stimulating hormone receptor (FSHr), and the androgen receptor (Ar). Adult male rats were orally treated with 1.0; 3.0 and 6.0 mg of PFOS kg(-1) d(-1) for 28 days. In general terms, PFOS can modify the relative gene and protein expressions of these receptors in several tissues of the reproductive axis. At the testicular level, apart from the expected inhibition of both gene and protein expressions of FSHr and Ar, PFOS also stimulates the GnRHr protein and the LHr gene expression. The receptors of the main hormones involved in the HPT axis may have an important role in the disruption exerted by PFOS on this axis.
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