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大鼠肝脏3-羟基-3-甲基戊二酰辅酶A还原酶的体内调节。胆固醇喂食后该酶的磷酸化作为早期调节反应。

The in vivo regulation of rat liver 3-hydroxy-3-methylglutaryl coenzyme A reductase. Phosphorylation of the enzyme as an early regulatory response following cholesterol feeding.

作者信息

Arebalo R E, Hardgrave J E, Scallen T J

出版信息

J Biol Chem. 1981 Jan 25;256(2):571-4.

PMID:6256360
Abstract

Although substantial evidence supports the conclusion that 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase is the major regulatory enzyme in cholesterol biosynthesis, the molecular events involved in the in vivo regulation of this enzyme have remained obscure. In order to study this problem, rats received a single meal consisting of either rat chow or rat chow containing 2% cholesterol. The rats were killed 60 or 120 min after the beginning of feeding, and liver microsomes were prepared by ultracentrifugation. Two phases of inhibition of microsomal HMG-CoA reductase were observed. The first phase of inhibition, observed 60 min after the beginning of cholesterol feeding, was completely reversed by preincubation of the microsomes with purified phosphoprotein phosphatase. The second phase of inhibition, observed 120 min after the beginning of cholesterol feeding, was not reversed by phosphoprotein phosphatase. These results are consistent with the conclusion that phosphorylation of HMG-CoA reductase is the first step in a series of in vivo regulatory events which produce inactivation and ultimately degradation of the enzyme.

摘要

尽管大量证据支持这样的结论,即3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶是胆固醇生物合成中的主要调节酶,但该酶在体内调节所涉及的分子事件仍不清楚。为了研究这个问题,给大鼠喂食一顿由普通大鼠饲料或含2%胆固醇的大鼠饲料组成的餐食。在开始喂食后60或120分钟处死大鼠,通过超速离心制备肝微粒体。观察到微粒体HMG-CoA还原酶受到两个阶段的抑制。在开始喂食胆固醇60分钟后观察到的第一阶段抑制,通过将微粒体与纯化的磷蛋白磷酸酶预孵育可完全逆转。在开始喂食胆固醇120分钟后观察到的第二阶段抑制,不能被磷蛋白磷酸酶逆转。这些结果与以下结论一致,即HMG-CoA还原酶的磷酸化是一系列体内调节事件的第一步,这些事件导致该酶失活并最终降解。

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