Niwa T, Naritomi Y, Kawano M, Ueda-Shimohira Y, Takeshita K, Shiraga T, Iwasaki K, Noda K
Pharmaceutical and Pharmacokinetic Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Osaka, Japan.
Res Commun Chem Pathol Pharmacol. 1994 Mar;83(3):341-8.
The effect of somatomedin C on the hepatic drug-metabolizing enzyme system in rat liver after sc injection, a clinically applicable dosing route, was studied. Although liver weight was slightly increased after somatomedin C (1 mg/kg) was injected for 7 days, no significant changes were observed in other dosing group (0.1 and 10 mg/kg). There were no significant effects of somatomedin C on cytochrome P-450 and b5 contents, and NADPH-cytochrome c reductase, aminopyrine demethylase, aniline hydroxylase, and ethoxyresorufin deethylase. Additionally, somatomedin C treatment did not affect the activities of 2 alpha-, 2 beta-, 6 beta- and 16 alpha-hydroxytestosterone and androstenedione formation from testosterone. Changes relation to dosing period were also examined with 1 mg/kg of somatomedin C. In this case, hepatic levels of cytochrome P-450 and b5, NADPH-cytochrome c reductase and drug oxidations did not differ significantly among groups treated for 3, 7, or 14 days. These results suggest that somatomedin C has no effect on the hepatic mixed-function oxidase system.
研究了生长调节素C经皮下注射(一种临床适用的给药途径)后对大鼠肝脏药物代谢酶系统的影响。尽管生长调节素C(1mg/kg)注射7天后肝脏重量略有增加,但其他给药组(0.1mg/kg和10mg/kg)未观察到明显变化。生长调节素C对细胞色素P-450和b5含量、NADPH-细胞色素c还原酶、氨基比林脱甲基酶、苯胺羟化酶和乙氧基试卤灵脱乙基酶均无显著影响。此外,生长调节素C处理不影响睾酮生成2α-、2β-、6β-和16α-羟基睾酮以及雄烯二酮的活性。还使用1mg/kg的生长调节素C研究了与给药期相关的变化。在这种情况下,细胞色素P-450和b5的肝脏水平、NADPH-细胞色素c还原酶和药物氧化在接受3天、7天或14天治疗的组之间没有显著差异。这些结果表明生长调节素C对肝脏混合功能氧化酶系统没有影响。