Imamura Y, Uchida A, Takada H, Otagiri M, Tsuchiya K
Faculty of Pharmaceutical Sciences, Kumamoto University, 5-1, Oe-honmachi, Kumamoto 862-0973, Japan.
Yakugaku Zasshi. 2001 Jan;121(1):85-91. doi: 10.1248/yakushi.121.85.
We examined physiological and genetic factors affecting acetohexamide reductase (AHR) and 20 beta-hydroxysteroid dehydrogenase (20 beta-HSD) activities in liver microsomes of experimental animals. Pronounced strain-related differences were found in both activities of AHR and 20 beta-HSD present in liver microsomes of male rats. Among rat strains tested in this study, even though a Wistar-Imamichi (WIM) rat strain was taken to lack AHR activity, it exhibited a significant 20 beta-HSD activity. These findings appeared to be in conflict with our conclusion reported so far, which AHR and 20 beta-HSD present in liver microsomes of male rats are identical enzymes. Thus the reason for this discrepancy was discussed. Furthermore, AHR and 20 beta-HSD activities were little or not observed in liver microsomes of female rats or male experimental animals other than the rat, indicating the existence of sex- and species-related differences in these two enzyme activities.
我们研究了影响实验动物肝脏微粒体中醋磺环己脲还原酶(AHR)和20β-羟基类固醇脱氢酶(20β-HSD)活性的生理和遗传因素。在雄性大鼠肝脏微粒体中,AHR和20β-HSD的活性均存在明显的品系相关差异。在本研究测试的大鼠品系中,尽管Wistar-Imamichi(WIM)大鼠品系被认为缺乏AHR活性,但它仍表现出显著的20β-HSD活性。这些发现似乎与我们迄今为止报道的结论相矛盾,即雄性大鼠肝脏微粒体中的AHR和20β-HSD是相同的酶。因此,讨论了这种差异的原因。此外,在雌性大鼠或除大鼠外的雄性实验动物的肝脏微粒体中,几乎未观察到AHR和20β-HSD活性,这表明这两种酶活性存在性别和物种相关差异。