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人良性前列腺增生(BPH)基质和上皮中的5α-雄甾烷-3β,17β-二醇羟化酶

5 alpha-androstane-3 beta,17 beta-diol hydroxylating enzymes in stroma and epithelium of human benign prostatic hyperplasia (BPH).

作者信息

Tunn S, Claus S, Schulze H, Braun B E, Krieg M

机构信息

Institute of Clinical Chemistry, University Clinic Bergmannsheil, Bochum, F.R.G.

出版信息

J Steroid Biochem. 1987 Sep;28(3):257-65. doi: 10.1016/0022-4731(87)91016-8.

Abstract

As enzymatic hydroxylation of 5 alpha-androstane-3 beta,17 beta-diol (3 beta-diol) may be a factor in controlling the 5 alpha-dihydrotestosterone (DHT) content in the prostate, we were interested in activity and distribution of these enzymes in epithelium and stroma of human benign prostatic hyperplasia (BPH). The enzyme activities were measured after mechanical separation of BPH tissue from 15 patients of various ages into stroma and epithelium, and optimization of the in vitro transformation of 3 beta-diol to hydroxylated products, which were analyzed by HPLC. The main results were: (1) 3 beta-diol was hydroxylated at C-7 alpha, C-7 beta, C-6 alpha, and C-6 beta. (2) The mean Michaelis constant Km (nM +/- SEM) for hydroxylation at C-7 alpha(beta) (168 +/- 21) was significantly lower than at C-6 alpha(beta) (601 +/- 43) without differences between stroma and epithelium. (3) Hydroxylation at alpha position dominated significantly over that at beta. (4) The mean maximal metabolic rate Vmax (pmol . mg protein-1 . h-1) of hydroxylation at C-6 alpha was about 7-fold lower in stroma (3.4 +/- 0.2) than in epithelium (23.8 +/- 4.1), concerning the other hydroxylations, Vmax was about 1.6-fold lower in stroma. (5) With increasing age of the patients there was a significant decrease of the 3 beta-diol hydroxylation in stroma and epithelium. It is discussed that the significantly lower activity of 3 beta-diol hydroxylation in stroma compared to epithelium and the decrease of activity with increasing age might potentiate the DHT accumulation in stroma of BPH.

摘要

由于5α-雄甾烷-3β,17β-二醇(3β-二醇)的酶促羟基化可能是控制前列腺中5α-双氢睾酮(DHT)含量的一个因素,我们对这些酶在人类良性前列腺增生(BPH)上皮和基质中的活性及分布感兴趣。在将15名不同年龄患者的BPH组织机械分离成基质和上皮后,测定酶活性,并优化3β-二醇向羟基化产物的体外转化,这些产物通过高效液相色谱法进行分析。主要结果如下:(1)3β-二醇在C-7α、C-7β、C-6α和C-6β位发生羟基化。(2)C-7α(β)位羟基化的平均米氏常数Km(nM±SEM)(168±21)显著低于C-6α(β)位(601±43),基质和上皮之间无差异。(3)α位的羟基化明显多于β位。(4)C-6α位羟基化的平均最大代谢速率Vmax(pmol·mg蛋白-1·h-1)在基质(3.4±0.2)中比在上皮(23.8±4.1)中低约7倍,对于其他羟基化反应,Vmax在基质中低约1.6倍。(5)随着患者年龄的增加,基质和上皮中3β-二醇的羟基化显著降低。讨论了与上皮相比,基质中3β-二醇羟基化活性显著较低以及活性随年龄增加而降低可能会增强BPH基质中DHT的积累。

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