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多不饱和脂肪酸和胆固醇对硬脂酰辅酶A去饱和酶的调节作用。

Regulation of stearoyl-CoA desaturase by polyunsaturated fatty acids and cholesterol.

作者信息

Ntambi J M

机构信息

Departments of Biochemistry and Nutritional Sciences, University of Wisconsin-Madison, Madison, WI 53706, USA.

出版信息

J Lipid Res. 1999 Sep;40(9):1549-58.

Abstract

The lipid composition of cellular membranes is regulated to maintain membrane fluidity. A key enzyme involved in this process is the membrane-bound stearoyl-CoA desaturase (SCD) which is the rate-limiting enzyme in the cellular synthesis of monounsaturated fatty acids from saturated fatty acids. A proper ratio of saturated to monounsaturated fatty acids contributes to membrane fluidity. Alterations in this ratio have been implicated in various disease states including cardiovascular disease, obesity, non-insulin-dependent diabetes mellitus, hypertension, neurological diseases, immune disorders, and cancer. The regulation of stearoyl-CoA desaturase is therefore of considerable physiological importance and its activity is sensitive to dietary changes, hormonal imbalance, developmental processes, temperature changes, metals, alcohol, peroxisomal proliferators, and phenolic compounds. Two mouse and rat SCD genes (SCD1 and SCD2) and a single human SCD gene have been cloned and characterized. In the past several years we have studied the dietary influences on the genetic expression of the mouse stearoyl-CoA desaturase. The expression of the mouse SCD genes is regulated by polyunsaturated fatty acids and cholesterol at the levels of transcription and mRNA stability. Promoter elements that are responsible for the polyunsaturated fatty acid repression colocalize with the promoter elements for SREBP-mediated regulation of the SCD genes. It is the goal of this review to provide an overview of the genetic regulation of the stearoyl-CoA desaturase in response to dietary polyunsaturated fatty acids and cholesterol.

摘要

细胞膜的脂质组成受到调控以维持膜的流动性。参与这一过程的关键酶是膜结合的硬脂酰辅酶A去饱和酶(SCD),它是细胞从饱和脂肪酸合成单不饱和脂肪酸过程中的限速酶。饱和脂肪酸与单不饱和脂肪酸的适当比例有助于维持膜的流动性。这种比例的改变与多种疾病状态有关,包括心血管疾病、肥胖症、非胰岛素依赖型糖尿病、高血压、神经疾病、免疫紊乱和癌症。因此,硬脂酰辅酶A去饱和酶的调控具有相当重要的生理意义,其活性对饮食变化、激素失衡、发育过程、温度变化、金属、酒精、过氧化物酶体增殖剂和酚类化合物敏感。已经克隆并鉴定了两个小鼠和大鼠的SCD基因(SCD1和SCD2)以及一个人类SCD基因。在过去的几年里,我们研究了饮食对小鼠硬脂酰辅酶A去饱和酶基因表达的影响。小鼠SCD基因的表达在转录和mRNA稳定性水平上受多不饱和脂肪酸和胆固醇的调控。负责多不饱和脂肪酸抑制作用的启动子元件与SREBP介导的SCD基因调控的启动子元件共定位。这篇综述的目的是概述硬脂酰辅酶A去饱和酶在响应饮食多不饱和脂肪酸和胆固醇时的基因调控情况。

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