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在硬脂酰辅酶A去饱和酶1基因缺失的小鼠中,生脂饮食揭示了甘油三酯合成对内源单不饱和脂肪酸的严格需求。

A lipogenic diet in mice with a disruption of the stearoyl-CoA desaturase 1 gene reveals a stringent requirement of endogenous monounsaturated fatty acids for triglyceride synthesis.

作者信息

Miyazaki M, Kim Y C, Ntambi J M

机构信息

Department of Biochemistry, University of Wisconsin, 433 Babcock Drive, Madison, WI 53706, USA.

出版信息

J Lipid Res. 2001 Jul;42(7):1018-24.

PMID:11441127
Abstract

Stearoyl-CoA desaturase (SCD) catalyzes the de novo biosynthesis of oleate and palmitoleate, which are the major fatty acids found in triglycerides, cholesteryl esters, and phospholipids. A high carbohydrate (lipogenic) diet induces lipogenic gene expression by sterol regulatory element binding protein 1 (SREBP-1c)-mediated gene transcription, leading to an increase in the synthesis of triglycerides. The lipogenic diet fed to mice with a null mutation in the SCD1 gene (SCD-/-) fails to induce the synthesis of triglycerides in liver, despite the induction of expression of SREBP-1 and its target genes, fatty acid synthase and glycerol-3-phosphate acyltransferase. The lipogenic diet led to a decrease in the levels of triglyceride, but an increase in the level of cholesteryl esters of saturated fatty acids. Feeding a lipogenic diet supplemented with high levels of oleate to the SCD-/- mice resulted in incorporation of oleate in the liver of SCD-/- mice, but failed to restore triglycerides to the levels in the normal mouse. Triglyceride synthesis, as measured by the incorporation of [(3)H]glycerol, was dramatically reduced in the liver of SCD-/- mouse fed a lipogenic diet compared with the normal mouse. These observations demonstrate that induction of triglyceride synthesis is highly dependent on SCD1 gene expression.

摘要

硬脂酰辅酶A去饱和酶(SCD)催化从头生物合成油酸和棕榈油酸,这两种是甘油三酯、胆固醇酯和磷脂中发现的主要脂肪酸。高碳水化合物(生脂)饮食通过固醇调节元件结合蛋白1(SREBP-1c)介导的基因转录诱导生脂基因表达,导致甘油三酯合成增加。给SCD1基因无效突变(SCD-/-)的小鼠喂食生脂饮食,尽管诱导了SREBP-1及其靶基因脂肪酸合酶和甘油-3-磷酸酰基转移酶的表达,但未能诱导肝脏中甘油三酯的合成。生脂饮食导致甘油三酯水平降低,但饱和脂肪酸胆固醇酯水平升高。给SCD-/-小鼠喂食补充高水平油酸的生脂饮食导致油酸掺入SCD-/-小鼠肝脏,但未能将甘油三酯恢复到正常小鼠的水平。与正常小鼠相比,喂食生脂饮食的SCD-/-小鼠肝脏中通过[(3)H]甘油掺入测量的甘油三酯合成显著降低。这些观察结果表明,甘油三酯合成的诱导高度依赖于SCD1基因表达。

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