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在给大鼠注射雌激素期间,对其肝脏类固醇代谢酶的性别依赖性活性变化进行的时间研究。

Time-studies of the changes in the sex-dependent activities of enzymes of hepatic steroid metabolism in the rat during oestrogen administration.

作者信息

Lax E R, Kreuzfelder E, Schriefers H

出版信息

Hoppe Seylers Z Physiol Chem. 1979 Dec;360(12):1807-17. doi: 10.1515/bchm2.1979.360.2.1807.

Abstract

This investigation was undertaken to elucidate the amount of oestradiol and duration of its administration necessary to cause complete feminization of the activities of cytoplasmic 3 alpha- and 17 beta-hydroxysteroid dehydrogenase, microsomal 3 alpha- and 3 beta-hydroxysteroid dehydrogenase and microsomal 5 alpha-reductase in male rat liver. With the exception of cytoplasmic 3 alpha-hydroxysteroid dehydrogenase, 5 microgram oestradiol/d for 8 days and less was sufficient to cause complete feminization. The order of oestrogen sensitivity was cytoplasmic 3 alpha-hydroxysteroid dehydrogenase greater than microsomal 3 beta-hydroxysteroid dehydrogenase greater than microsomal 3 alpha-hydroxysteroid dehydrogenase greater than microsomal 5 alpha-reductase greater than cytoplasmic 17 beta-hydroxysteroid dehydrogenase. Although the changes occurring after oestradiol administration are qualitatively the same as after testectomy, they occur more rapidly. This rules out the possibility that oestradiol exerts its effect via androgen deprivation. Diethylstilboestrol administration causes the same changes in cytoplasmic 17 beta- and microsomal 3 beta-hydroxysteroid dehydrogenase activity as oestradiol, although the dosage must be increased 100 fold. The effect of diethylstilboestrol on 5 alpha-reductase activity changes with the dose applied. Doses up to 100 microgram/d partially feminize the activity, but at higher doses the enzyme activity is repressed.

摘要

本研究旨在阐明使雄性大鼠肝脏细胞质3α-和17β-羟基类固醇脱氢酶、微粒体3α-和3β-羟基类固醇脱氢酶以及微粒体5α-还原酶的活性完全雌性化所需的雌二醇量及其给药持续时间。除细胞质3α-羟基类固醇脱氢酶外,每天5微克雌二醇,给药8天及以下就足以导致完全雌性化。雌激素敏感性顺序为:细胞质3α-羟基类固醇脱氢酶>微粒体3β-羟基类固醇脱氢酶>微粒体3α-羟基类固醇脱氢酶>微粒体5α-还原酶>细胞质17β-羟基类固醇脱氢酶。虽然给予雌二醇后发生的变化在性质上与睾丸切除后相同,但变化发生得更快。这排除了雌二醇通过雄激素剥夺发挥作用的可能性。给予己烯雌酚会使细胞质17β-和微粒体3β-羟基类固醇脱氢酶活性产生与雌二醇相同的变化,尽管剂量必须增加100倍。己烯雌酚对5α-还原酶活性的影响随给药剂量而变化。每天剂量达100微克时可使该酶活性部分雌性化,但剂量更高时酶活性受到抑制。

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