Altwein J E, Orestano F
Urol Res. 1975;2(4):143-8. doi: 10.1007/BF00257262.
An in vitro system for testing steroids which might be effective in treating benign prostatic hypertrophy (BPH) has been developed based upon the transformation of H-3-testosterone into the 5-alpha-reduction products dihydrotestosterone and 3-alpha-androstanediol. In scrutinizing the influence of the amount of BPH-tissue, time, and pH, 300 mg of tissue incubated for 2 h at the physiological pH of 7.4 were used in the standard experiment. -The H-3-testosterone concentration was varied from 0.17-100 times 10-8 M. Plotting the resulting 5-alpha-reduction products as a function of testosterone concentration a hyperbolic pattern of enzyme kinetics ensued. Performing a double reciprocal plot of 4 experiments with double determination of each value regression lines could be computed. Those two regression lines most different in their slopes were considered "normal" limits. The rate of H-3-testosterone metabolism could not be enhanced after the endogenous testosterone content within the prostate glands had been used up by means of a preincubation. Scrutinizing the effect of heparin, a weak non-specific enzyme inhibitor, no suppression of the appearance of 5-alpha-reduction products was found. Damaging the BPH-cells, however, by repetitive freezing and thawing lead to an almost complete inhibition of H-3-testosterone turnover.
基于将H-3-睾酮转化为5-α-还原产物二氢睾酮和3-α-雄烷二醇,已开发出一种体外系统来测试可能对治疗良性前列腺增生(BPH)有效的类固醇。在研究BPH组织量、时间和pH值的影响时,标准实验使用300mg组织在生理pH值7.4下孵育2小时。H-3-睾酮浓度在0.17至100×10-8M之间变化。将所得的5-α-还原产物绘制为睾酮浓度的函数,呈现出酶动力学的双曲线模式。对4次实验进行双倒数作图,每次值进行双份测定,可以计算出回归线。斜率差异最大的两条回归线被视为“正常”范围。通过预孵育耗尽前列腺内源性睾酮含量后,H-3-睾酮的代谢速率无法提高。研究弱非特异性酶抑制剂肝素的作用时,未发现对5-α-还原产物出现的抑制作用。然而,通过反复冻融破坏BPH细胞会导致H-3-睾酮周转几乎完全抑制。