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大鼠肝微粒体对辛伐他汀代谢的性别差异。

Sex difference in metabolism of simvastatin by rat hepatic microsomes.

作者信息

Ohtawa M, Uchiyama N

机构信息

Department of Drug Metabolism, Banyu Pharmaceutical Co Ltd, Tokyo, Japan.

出版信息

Eur J Drug Metab Pharmacokinet. 1992 Jul-Sep;17(3):175-81. doi: 10.1007/BF03190142.

Abstract

Metabolism of simvastatin (SV), a new cholesterol-lowering agent, by hepatic microsomes from male and female rats was investigated. After incubation of [14C]-SV with hepatic microsomes, radioactive metabolites were detected by HPLC. The main metabolite was 3' alpha-hydroxy-SV in male rats and the hydroxy open acid form of SV (SVA) in females. The 3"-hydroxy-SV and 3',3"-dihydroxy-SV which were observed in male rats were hardly detected in females. Specific activity for the metabolism of SV in male rats (3.97 nmol/mg protein/min) was about 9-times higher than that in females. Metabolic activity of hepatic microsomes in male rats was essentially unchanged with increase in age, whereas that in females decreased age-dependently and was very low or negligible after 7 weeks of age. Formation of 3"-hydroxy-SV and 3',3"-dihydroxy-SV in male rats was markedly increased with age, and that in females was negligible at all ages examined.

摘要

研究了新型降胆固醇药物辛伐他汀(SV)在雄性和雌性大鼠肝脏微粒体中的代谢情况。将[14C] - SV与肝脏微粒体孵育后,通过高效液相色谱法检测放射性代谢产物。雄性大鼠的主要代谢产物是3'α - 羟基 - SV,雌性大鼠的主要代谢产物是SV的羟基开环酸形式(SVA)。在雄性大鼠中观察到的3'' - 羟基 - SV和3',3'' - 二羟基 - SV在雌性大鼠中几乎检测不到。雄性大鼠中SV代谢的比活性(3.97 nmol/mg蛋白/分钟)约为雌性大鼠的9倍。雄性大鼠肝脏微粒体的代谢活性随年龄增长基本不变,而雌性大鼠的代谢活性则随年龄依赖性降低,7周龄后非常低或可忽略不计。雄性大鼠中3'' - 羟基 - SV和3',3'' - 二羟基 - SV的形成随年龄显著增加,而在所有检查年龄的雌性大鼠中均可忽略不计。

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