Tunn S, Haumann R, Hey J, Flüchter S H, Krieg M
Institute of Clinical Chemistry and Laboratory Medicine, University Clinic Bergmannsheil, Bochum, West Germany.
J Clin Endocrinol Metab. 1990 Sep;71(3):732-9. doi: 10.1210/jcem-71-3-732.
The accumulation of 5 alpha-dihydrotestosterone (DHT), particularly in stroma, is a possible etiological factor in regard of the age-dependent development of benign prostatic hyperplasia (BPH). In this context, we have recently demonstrated age-dependent alterations of 5 alpha-reductase, which is responsible for the irreversible conversion of testosterone to DHT. Therefore, it was also of interest to study possible age-dependent alterations of those enzymes mainly involved in the reversible metabolism of DHT to 5 alpha-androstanediols. Thus, we determined, in the presence of NADPH/NADP+, kinetic parameters [Km and maximum velocity (Vmax)] of 3-hydroxysteroid oxidoreductases (3 alpha-HSORred, 3 beta-HSORred, and 3 alpha-HSORox) in separated epithelium and stroma of 10 normal (NPR) and 20 hyperplastic prostates (BPH) and correlated the data with the age of the donors (15-86 yr). The mean Km (nanomolar concentrations +/- SEM) of 3 alpha-HSORred was significantly (P less than 0.01) higher in epithelium (NPR, 1391 +/- 181; BPH, 2150 +/- 157) than in stroma (NPR, 778 +/- 22; BPH, 749 +/- 62), indicating the presence of epithelial and stromal enzymes. The mean Km values of 3 beta-HSORred and 3 alpha-HSORox were similar. Concerning 3 alpha-HSORred, the mean potential capacity, i.e. the quotient of Vmax/Km (+/- SEM), was significantly (P less than 0.01) higher in epithelium (0.56 +/- 0.08) than in stroma (0.19 +/- 0.02) of NPR, while in BPH nearly identical mean potential capacities were found in epithelium (0.33 +/- 0.04) and stroma (0.26 +/- 0.02). The respective Vmax/Km of 3 beta-HSORred and 3 alpha-HSORox were significantly (P less than 0.05) lower. In addition, the potential capacity of all three enzymes was distinctly lower than the potential DHT-forming capacity of 5 alpha-reductase. With advancing age, the Vmax/Km decreased significantly (P less than 0.001; 3 alpha-HSORred and 3 beta-HSORred) or tendentiously (3 alpha-HSORox) in epithelium, while in stroma a significant (P less than 0.001; 3 alpha-HSORred and 3 alpha-HSORox) or tendentious (3 beta-HSORred) increase with age was found. Our results indicate that aging has a significant impact on DHT-removing enzymes. However, these enzymes counterbalance only in part the strong potential capacity of 5 alpha-reductase.
5α - 二氢睾酮(DHT)的蓄积,尤其是在基质中的蓄积,可能是良性前列腺增生(BPH)随年龄发展的一个病因。在这种情况下,我们最近证实了5α - 还原酶存在年龄依赖性改变,该酶负责睾酮向DHT的不可逆转化。因此,研究那些主要参与DHT可逆代谢生成5α - 雄甾二醇的酶可能存在的年龄依赖性改变也很有意义。于是,我们在存在NADPH/NADP⁺的情况下,测定了10例正常前列腺(NPR)和20例增生性前列腺(BPH)的分离上皮和基质中3 - 羟基类固醇氧化还原酶(3α - HSORred、3β - HSORred和3α - HSORox)的动力学参数[米氏常数(Km)和最大速度(Vmax)],并将数据与供体年龄(15 - 86岁)相关联。3α - HSORred的平均Km(纳摩尔浓度±标准误)在上皮中(NPR,1391±181;BPH,2150±157)显著高于基质(NPR,778±22;BPH,749±62)(P<0.01),表明存在上皮和基质酶。3β - HSORred和3α - HSORox的平均Km值相似。关于3α - HSORred,平均潜在能力,即Vmax/Km(±标准误),在NPR的上皮中(0.56±0.08)显著高于基质(0.19±0.02)(P<0.01),而在BPH中,上皮(0.33±0.04)和基质(0.26±0.02)的平均潜在能力几乎相同。3β - HSORred和3α - HSORox各自的Vmax/Km显著更低(P<0.05)。此外,这三种酶的潜在能力明显低于5α - 还原酶的潜在DHT生成能力。随着年龄增长,上皮中Vmax/Km显著降低(P<0.001;3α - HSORred和3β - HSORred)或呈趋势性降低(3α - HSORox),而在基质中,随着年龄增长发现显著增加(P<0.001;3α - HSORred和3α - HSORox)或呈趋势性增加(3β - HSORred)。我们的结果表明,衰老对DHT去除酶有显著影响。然而,这些酶仅部分抵消了5α - 还原酶强大的潜在能力。