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Tetrahydrogestrinone is a Potent Androgen and Progestin.

机译:四氢孕酮是有效的雄激素和孕激素。

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摘要

Tetrahydrogestrinone (THG) is a recently discovered steroid that has never been marketed and is used unlawfully to enhance sports performance. Structurally, THG resembles trenbolone, a veterinary androgen. Using a yeast-based in vitro bioassay, the investigators examined the biologic interactions of THG with the human androgen receptor (AR), progesterone receptor (PR), and estrogen receptor (ER). THG agonist activity in the AR bioassay was compared with that of gestrinone, its parent compound, the structurally similar steroid trenbolone, and nandrolone, used as a positive androgen control.THG strongly activated AR transactivation when compared with the other steroids. THG exhibited progestin activity that was 7-fold greater than that of progesterone. In contrast, gestrinone and trenbolone had much less progestin activity than progesterone. THG did not inhibit activation of the androgen receptor by testosterone or activation of the progesterone receptor by progesterone. No ER agonist or antagonist activity was observed. None of the steroids caused cellular toxicity.These findings indicate that THG is a potent androgen and progestin. It does not alter ER action and has no antagonistic effects against any of the sex steroid receptors. The discovery of this designer androgen prompts concern that a range of novel androgens might be produced from marketed progestins and other synthetic sex steroids.
机译:四氢孕酮(THG)是最近发现的类固醇,从未上市,可非法用于增强运动表现。 THG在结构上类似于群勃龙,一种兽医雄激素。研究人员使用基于酵母的体外生物测定法检查了THG与人类雄激素受体(AR),孕激素受体(PR)和雌激素受体(ER)的生物学相互作用。将AR生物测定中的THG激动剂活性与孕激素,其母体化合物,结构相似的类固醇群勃龙和nandrolone用作雄激素阳性对照进行了比较。与其他类固醇相比,THG强烈激活了AR反式激活。 THG的孕激素活性比孕酮高7倍。相反,孕酮和群勃龙的孕激素活性远低于孕酮。 THG不会抑制睾丸激素对雄激素受体的激活,也不会抑制黄体酮对孕激素受体的激活。没有观察到ER激动剂或拮抗剂活性。这些类固醇均未引起细胞毒性。这些发现表明THG是有效的雄激素和孕激素。它不会改变ER作用,对任何性类固醇受体也没有拮抗作用。该雄激素的设计者的发现引起了人们的关注,即可能从市售的孕激素和其他合成性类固醇中产生一系列新型雄激素。

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