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3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂MK-733(辛伐他汀)对兔肠道酰基辅酶A:胆固醇酰基转移酶活性的影响。

Effects of MK-733 (simvastatin), an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase, on intestinal acylcoenzyme A:cholesterol acyltransferase activity in rabbits.

作者信息

Ishida F, Sato A, Iizuka Y, Kitani K, Sawasaki Y, Kamei T

机构信息

Central Research Laboratories, Banyu Pharmaceutical Co., Ltd., Tokyo, Japan.

出版信息

Biochim Biophys Acta. 1989 Jul 17;1004(1):117-23. doi: 10.1016/0005-2760(89)90221-x.

Abstract

MK-733 (simvastatin), a potent 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor, was found to inhibit the absorption of cholesterol from the gastrointestinal tract in cholesterol-fed rabbits (Ishida et al. (1988) Biochim. Biophys. Acta 963, 35-41). To clarify the mechanism of action, the effects of MK-733 on acyl coenzyme A:cholesterol acyltransferase (ACAT) and cholesterol esterase activities, which are thought to participate in the absorption of cholesterol, were examined. Dietary administration (0.03% in a 1% cholesterol diet for 7 days, approx. 10 mg/kg) of MK-733 to cholesterol-fed rabbits was found to inhibit the increase in serum total cholesterol levels, and caused a 70% reduction in ACAT activity in microsomes of intestinal mucosa relative to those observed in concurrent control rabbits. MK-733 did not affect cholesterol esterase activity in the cytosol of the intestinal mucosa. The inhibitory effect of MK-733 on cholesterol absorption in cholesterol-fed rabbits is though to be related to a reduction in microsomal ACAT activity in the intestinal mucosa.

摘要

MK-733(辛伐他汀)是一种强效的3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂,研究发现它能抑制胆固醇喂养的兔子胃肠道对胆固醇的吸收(Ishida等人,(1988年)《生物化学与生物物理学报》963卷,第35 - 41页)。为了阐明其作用机制,研究了MK-733对酰基辅酶A:胆固醇酰基转移酶(ACAT)和胆固醇酯酶活性的影响,这两种酶被认为参与了胆固醇的吸收过程。给胆固醇喂养的兔子进行膳食给药(在1%胆固醇饮食中添加0.03%,持续7天,约10毫克/千克)MK-733,结果发现它能抑制血清总胆固醇水平的升高,并使肠黏膜微粒体中的ACAT活性相对于同期对照兔子降低了70%。MK-733对肠黏膜细胞质中的胆固醇酯酶活性没有影响。MK-733对胆固醇喂养兔子胆固醇吸收的抑制作用被认为与肠黏膜微粒体ACAT活性的降低有关。

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