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开蓬和灭蚁灵对Y-1细胞类固醇合成的抑制作用。

Inhibitory effect of chlordecone and mirex on steroid synthesis in Y-1 cells.

作者信息

Warner W

出版信息

J Environ Pathol Toxicol Oncol. 1987 Mar-Apr;7(4):47-54.

PMID:2439679
Abstract

Chlordecone is known to bring about alterations in the endocrine systems of a variety of animals. The present study was undertaken to investigate the possibility of a direct effect of the insecticide on steroid-secreting tissues. Technical grade chlordecone produced a dose-dependent inhibition of steroidogenesis in cultured mouse adrenal tumor cells (Y-1 cells) when stimulated with ACTH (IC50 = 4 X 10(-5) M), cAMP (IC50 = 2.3 X 10(-5) M), or pregnenolone (IC50 3.5 X 10(-5) M). Similar values were obtained with 99% pure chlordecone. These data suggest that chlordecone inhibited the conversion of pregnenolone into 20 alpha-dihydroprogesterone. Additional sites of action cannot be ruled out. Mirex failed to inhibit steroidogenesis which was supported by exogenous pregnenolone. At a concentration of 3 X 10(-6) M mirex inhibited cAMP induced steroidogenesis, but higher concentrations did not produce a more pronounced effect.

摘要

已知开蓬会引起多种动物内分泌系统的改变。本研究旨在调查该杀虫剂对类固醇分泌组织的直接影响。当用促肾上腺皮质激素(ACTH,半数抑制浓度[IC50]=4×10⁻⁵M)、环磷酸腺苷(cAMP,IC50 = 2.3×10⁻⁵M)或孕烯醇酮(IC50 = 3.5×10⁻⁵M)刺激时,工业级开蓬对培养的小鼠肾上腺肿瘤细胞(Y-1细胞)的类固醇生成产生剂量依赖性抑制。使用99%纯开蓬也获得了类似数值。这些数据表明,开蓬抑制了孕烯醇酮向20α-二氢孕酮的转化。不能排除其他作用位点。灭蚁灵未能抑制由外源性孕烯醇酮支持的类固醇生成。在浓度为3×10⁻⁶M时,灭蚁灵抑制了cAMP诱导的类固醇生成,但更高浓度并未产生更明显的效果。

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