Dansette P M, Jaoen M, Pons C
Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, URA 400 CNRS, Université Rene Descartes, Paris, France.
Exp Toxicol Pathol. 2000 May;52(2):145-8. doi: 10.1016/S0940-2993(00)80107-4.
The aim of this study was to compare a number of vastatins, HMG-CoA reductase inhibitors, in human liver microsomes. HMG-CoA reductase activity was four times lower than the activity in untreated rat liver microsomes. Vastatins could be classified in this in vitro assay in three classes both in human and rat microsomes: the first one including cerivastatin with an IC50 of 6 nM, the second one with atorvastatin and fluvastatin (IC50) between 40 and 100 nM) and the third one containing pravastatin, simvastatin and lovastatin (IC50 between 100 and 300 nM).
本研究的目的是在人肝微粒体中比较多种他汀类药物(HMG-CoA还原酶抑制剂)。HMG-CoA还原酶活性比未处理的大鼠肝微粒体中的活性低四倍。在该体外试验中,他汀类药物在人和大鼠微粒体中均可分为三类:第一类包括西立伐他汀,IC50为6 nM;第二类包括阿托伐他汀和氟伐他汀(IC50在40至100 nM之间);第三类包括普伐他汀、辛伐他汀和洛伐他汀(IC50在100至300 nM之间)。