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达那唑抑制类固醇生成。

Danazol inhibits steroidogenesis.

作者信息

Barbieri R L, Canick J A, Makris A, Todd R B, Davies I J, Ryan K J

出版信息

Fertil Steril. 1977 Aug;28(8):809-13.

PMID:885271
Abstract

Danazol was found to inhibit multiple enzymes of steroidogenesis directly in the pregnant mare serum (PMS)-treated hamster ovary and the rat testis and adrenal in vitro. In the PMS-treated hamster ovary, danazol inhibited 17alpha-hydroxylase, 17,20-lyase, and 3beta-hydroxysteroid dehydrogenase. In the rat testis, danazol inhibited 17alpha-hydroxylase, 17,20-lyase, 3beta-hydroxysteroid dehydrogenase, and 17beta-hydroxysteroid dehydrogenase. In the rat adrenal, danazol inhibited 3beta-hydroxysteroid dehydrogenase, 21-hydroxylase, and 11beta-hydroxylase. Two hours after a subcutaneous injection of 5 mg/kg of danazol to adult male rats, serum luteinizing hormone levels were significantly increased and serum testosterone levels were significantly suppressed. These findings suggest that in the rodent one of danazol's major pharmacologic effects is the direct inhibition of steroidogenesis.

摘要

已发现达那唑在体外可直接抑制经孕马血清(PMS)处理的仓鼠卵巢、大鼠睾丸及肾上腺中的多种甾体生成酶。在经PMS处理的仓鼠卵巢中,达那唑可抑制17α-羟化酶、17,20-裂解酶及3β-羟类固醇脱氢酶。在大鼠睾丸中,达那唑可抑制17α-羟化酶、17,20-裂解酶、3β-羟类固醇脱氢酶及17β-羟类固醇脱氢酶。在大鼠肾上腺中,达那唑可抑制3β-羟类固醇脱氢酶、21-羟化酶及11β-羟化酶。给成年雄性大鼠皮下注射5mg/kg达那唑两小时后,血清促黄体生成素水平显著升高,血清睾酮水平显著降低。这些发现表明,在啮齿动物中,达那唑的主要药理作用之一是直接抑制甾体生成。

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