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人类附睾的研究:3α-和3β-羟基类固醇脱氢酶的部分特性、5α-还原酶的区域分布以及4δ-3-氧代类固醇对5α-还原酶的抑制作用

Studies on the human epididymis: partial characterization of 3 alpha- and 3 beta-hydroxysteroid dehydrogenase, regional distribution of 5 alpha-reductase and inhibitory effect of 4 delta-3-oxosteroids on 5 alpha-reductase.

作者信息

Kinoshita Y

出版信息

Endocrinol Jpn. 1981 Aug;28(4):499-513. doi: 10.1507/endocrj1954.28.499.

Abstract

When [4-14C]-5 alpha-dihydrotestosterone was incubated with the homogenate of human epididymis, 5 alpha-androstane-3 alpha, 17 beta-diol and 5 alpha-androstane-3 beta, 17 beta-diol were identified as major metabolites. The ratio of 3 alpha- to 3 beta-epimer in androstanediol formation was approximately 2.4. 5 alpha-Androstane-3, 17-dione was also identified as a minor metabolite. Among the subcellular fractions, both the human epididymal 3 alpha- and 3 beta-hydroxysteroid dehydrogenases were localized almost exclusively in the cytosol fraction (105,000 X g supernatant). Both enzymes had optimum pH at 7.5 and optimum temperature at 46 degrees C. NADPH was a more preferable cofactor than NADH for both dehydrogenases. The Michaelis constants (Km) of 3 alpha- and 3 beta-hydroxysteroid dehydrogenase for 5 alpha-dihydrotestosterone were similar and estimated as 8 X 10(-5) M, but the enzymes were unsaturable with the substrate under the conditions investigated, indicating low affinity and high capacity of both dehydrogenases for 5 alpha-dihydrotestosterone. The human epididymal 5 alpha-reductase revealed a regional difference in activity. The 5 alpha-reductase activity in the most proximal part of the head (ductuli efferentes) was one seventh to one tenth the activity in the remaining part of the epididymis which was constructed of ductus epididymis. Except for this finding, the activity of 5 alpha-reductase was highest in the head, then declined along the course to the tail portion. The 5 alpha-reductase for testosterone was competitively inhibited by delta 4-3-oxosteroids such as progesterone, 20 alpha-dihydroprogesterone, 17 alpha-hydroxyprogesterone, 4-androstenedione, 11-deoxycorticosterone, corticosterone and 11-deoxycortisol, which had inhibition constants (Ki) of 3.3 X 10(-9) M, 2.2 X 10(-9) M, 1.8 X 10(-8) M, 1.3 X 10(-8) M, 8.3 X 10(-9) M, 1.5 X 10(-7) M and 8.7 X 10(-8) M, respectively, suggesting the possibility that the 5 alpha-reduction of testosterone is regulated by other delta 4-3-oxosteroids.

摘要

当用[4-¹⁴C]-5α-双氢睾酮与人附睾匀浆一起温育时,5α-雄甾烷-3α,17β-二醇和5α-雄甾烷-3β,17β-二醇被鉴定为主要代谢产物。雄甾二醇形成过程中3α-差向异构体与3β-差向异构体的比例约为2.4。5α-雄甾烷-3,17-二酮也被鉴定为次要代谢产物。在亚细胞组分中,人附睾的3α-和3β-羟基类固醇脱氢酶几乎都定位于胞质溶胶组分(105,000×g上清液)。两种酶的最适pH均为7.5,最适温度为46℃。对于两种脱氢酶来说,NADPH是比NADH更合适的辅因子。3α-和3β-羟基类固醇脱氢酶对5α-双氢睾酮的米氏常数(Km)相似,估计为8×10⁻⁵M,但在所研究的条件下,底物不能使酶饱和,这表明两种脱氢酶对5α-双氢睾酮的亲和力低、容量高。人附睾5α-还原酶的活性存在区域差异。头部最近端部分(输出小管)的5α-还原酶活性是由附睾管构成的附睾其余部分活性的七分之一到十分之一。除了这一发现外,5α-还原酶的活性在头部最高,然后沿附睾向尾部逐渐下降。睾酮的5α-还原酶受到δ⁴-3-氧代类固醇如孕酮、20α-二氢孕酮、17α-羟基孕酮、4-雄烯二酮、11-脱氧皮质酮、皮质酮和11-脱氧皮质醇的竞争性抑制,它们的抑制常数(Ki)分别为3.3×10⁻⁹M、2.2×10⁻⁹M、1.8×10⁻⁸M、1.3×10⁻⁸M、8.3×10⁻⁹M、1.5×10⁻⁷M和8.7×10⁻⁸M,这表明睾酮的5α-还原可能受其他δ⁴-3-氧代类固醇调节。

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