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消胆胺和洛伐他汀对大鼠肝脏3-羟基-3-甲基戊二酰辅酶A还原酶昼夜周期的影响。

The effect of cholestyramine and Mevinolin on the diurnal cycle of rat hepatic 3-hydroxy-3-methylglutaryl coenzyme A reductase.

作者信息

Tanaka R D, Edwards P A, Lan S F, Knöppel E M, Fogelman A M

出版信息

J Lipid Res. 1982 Sep;23(7):1026-31.

PMID:6923909
Abstract

Rats were fed powdered rat chow or a rat chow diet containing 5% cholestyramine or 5% cholestyramine with Mevinolin (112 mg/100 g food, 200 mg/kg body weight per day). The specific activity of hepatic 3-hydroxy-3-methylglutaryl coenzyme A reductase was determined at different times during the diurnal cycle of the enzyme. Animals fed cholestyramine had higher specific activities of HMG-CoA reductase at all time points tested when compared to controls. The specific activity at the peak in the diurnal cycle was approximately 8-fold higher in cholestyramine-treated animals. Rats administered the cholestyramine-Mevinolin diet had higher specific activities of the enzyme than either cholestyramine-treated or control animals. In the cholestyramine-Mevinolin-treated animals the peak in the diurnal cycle was shifted to D-12 (12th hour of the dark cycle) and the specific activity at this point was approximately 133-fold greater than the basal (L-6) activity in control animals. Optimal conditions for immunotitration studies were determined such that valid conclusions could be drawn from these data. Based on immunotitration experiments, the increased hepatic HMG-CoA reductase activity in cholestyramine-treated animals resulted in part from a 3-fold activation of the enzyme, while the increased specific activity in the cholestyramine-Mevinolin-treated animals was due solely to increased enzyme mass. Hence the administration of Mevinolin blocked the activation of the enzyme induced by feeding cholestyramine alone. This was confirmed by purifying the enzyme to apparent homogeneity from cholestyramine-Mevinolin-treated animals; the specific activity of this enzyme was 4,000-7,700 nmol NADPH oxidized/min per mg protein. Cholestyramine-Mevinolin treatment affords a novel system for generating milligram quantities of rat hepatic HMG-CoA reductase.-Tanaka, R. D., P. A. Edwards, S. Lan, E. M. Knöppel, and A. M. Fogelman. The effect of cholestyramine and Mevinolin on the diurnal cycle of rat hepatic 3-hydroxy-3-methylglutaryl coenzyme A reductase.

摘要

给大鼠喂食大鼠饲料粉末,或喂食含5%消胆胺的大鼠饲料,或喂食含5%消胆胺与美伐他汀(112毫克/100克食物,每天200毫克/千克体重)的大鼠饲料。在肝脏3-羟基-3-甲基戊二酰辅酶A还原酶昼夜循环的不同时间测定其比活性。与对照组相比,喂食消胆胺的动物在所有测试时间点的HMG-CoA还原酶比活性均较高。消胆胺处理组动物在昼夜循环峰值时的比活性比对照组高约8倍。喂食消胆胺-美伐他汀饲料的大鼠,该酶的比活性高于消胆胺处理组或对照组动物。在消胆胺-美伐他汀处理的动物中,昼夜循环峰值移至D-12(黑暗周期的第12小时),此时的比活性比对照组动物的基础(L-6)活性高约133倍。确定了免疫滴定研究的最佳条件,以便能从这些数据得出有效结论。基于免疫滴定实验,消胆胺处理组动物肝脏HMG-CoA还原酶活性增加部分是由于该酶3倍的激活,而消胆胺-美伐他汀处理组动物比活性增加仅归因于酶量增加。因此,美伐他汀的给药阻断了单独喂食消胆胺诱导的酶激活。从消胆胺-美伐他汀处理的动物中纯化该酶至表观均一性证实了这一点;该酶的比活性为4000 - 7700纳摩尔NADPH氧化/分钟/毫克蛋白质。消胆胺-美伐他汀处理提供了一种产生毫克量大鼠肝脏HMG-CoA还原酶的新系统。——田中,R.D.,P.A.爱德华兹,S.兰,E.M.克诺佩尔,和A.M.福格尔曼。消胆胺和美伐他汀对大鼠肝脏3-羟基-3-甲基戊二酰辅酶A还原酶昼夜循环的影响

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