Molecular Endocrinology Laboratory, Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee 247 667, Uttarakhand, India.
J Steroid Biochem Mol Biol. 2010 May;120(1):22-9. doi: 10.1016/j.jsbmb.2010.02.032. Epub 2010 Mar 6.
The present work describes the screening and characterization of some common endocrine disrupting chemicals for their (anti)androgenic activities. Various chemicals (mostly pesticides and pharmaceuticals) were screened with the NIH3T3 cell line stably expressing human androgen receptor (hAR) and luciferase reporter gene for their ability to stimulate luciferase activity or inhibit the response that was evoked by 0.4nM testosterone. The most potent anti-androgenic compounds identified in our assay included chlorpyrifos, endosulfan and piperophos. Finally, the chemicals were analyzed for their effects on steriodogenesis in rat Leydig cells. Piperophos and chlorpyrifos showed a significant decrease in testosterone biosynthesis by Leydig cells. RT-PCR studies showed decrease in the expression of key steroidogenic enzymes: cytochrome P450scc, 3beta-HSD and 17beta-HSD and immunoblot analysis demonstrated a decrease in steroidogenic acute regulatory (StAR) protein expression by both these chemicals. Chlorpyrifos also showed a decrease in LH receptor stimulated cAMP production. In conclusion, we demonstrate that commonly used pesticides like chlorpyrifos and piperophos pose serious threat to male reproductive system by interfering at various levels of androgen biosynthesis.
本工作描述了一些常见的内分泌干扰化学物质的筛选和特性,以研究它们的(抗)雄激素活性。使用稳定表达人雄激素受体(hAR)和荧光素酶报告基因的 NIH3T3 细胞系,筛选各种化学物质(主要是农药和药物),以研究它们刺激荧光素酶活性或抑制 0.4nM 睾丸酮引起的反应的能力。在我们的测定中,鉴定出的最有效的抗雄激素化合物包括氯蜱磷、硫丹和哌虫磷。最后,分析了这些化学物质对大鼠睾丸间质细胞类固醇生成的影响。哌虫磷和氯蜱磷显著降低了睾丸间质细胞的睾丸酮生物合成。RT-PCR 研究表明,关键类固醇生成酶的表达减少:细胞色素 P450scc、3β-HSD 和 17β-HSD,免疫印迹分析表明这两种化学物质均降低了类固醇生成急性调节蛋白(StAR)的表达。氯蜱磷还降低了 LH 受体刺激的 cAMP 产生。总之,我们证明了像氯蜱磷和哌虫磷这样常用的农药通过干扰雄激素生物合成的各个水平,对男性生殖系统构成严重威胁。