首页> 外文期刊>Diabetes >Overexpression of Carnitine Palmitoyltransferase-1 in Skeletal Muscle Is Sufficient to Enhance Fatty Acid Oxidation and Improve High-Fat Diet-Induced Insulin Resistance
【24h】

Overexpression of Carnitine Palmitoyltransferase-1 in Skeletal Muscle Is Sufficient to Enhance Fatty Acid Oxidation and Improve High-Fat Diet-Induced Insulin Resistance

机译:骨骼肌中肉碱棕榈酰转移酶-1的过表达足以增强脂肪酸氧化并改善高脂饮食诱导的胰岛素抵抗

获取原文
获取原文并翻译 | 示例
           

摘要

Skeletal muscle insulin resistance is associated with lipid accumulation, but whether insulin resistance is due to reduced or enhanced flux of long-chain fatty acids into the mitochondria is both controversial and unclear. We hypothesized that skeletal muscle-specific overexpression of the muscle isoform of carnitine palmitoyltransferase 1 (CPT1), the enzyme that controls the entry of long-chain fatty acyl CoA into mitochondria, would enhance rates of fatty acid oxidation and improve insulin action in muscle in high-fat diet insulin-resistant rats.
机译:骨骼肌胰岛素抵抗与脂质蓄积有关,但胰岛素抵抗是由于长链脂肪酸进入线粒体的通量减少还是增加是有争议的,也不清楚。我们假设肉碱棕榈酰转移酶1(CPT1)是控制长链脂肪酰基辅酶A进入线粒体的酶的骨骼肌特异性过表达,会提高脂肪酸氧化速率并改善胰岛素在肌肉中的作用。高脂饮食对胰岛素抵抗的大鼠。

著录项

  • 来源
    《Diabetes》 |2009年第3期|p.550-558|共9页
  • 作者单位

    Clinton R. Bruce,1,2 Andrew J. Hoy,2 Nigel Turner,2 Matthew J. Watt,3,4 Tamara L. Allen,1 Kevin Carpenter,5,6 Gregory J. Cooney,2 Mark A. Febbraio,1 and Edward W. Kraegen2From the 1 Cellular and Molecular Metabolism Laboratory, Baker IDI Heart and Diabetes Institute, Melbourne, Victoria, Australia, the 2 Diabetes and Obesity Program, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia, 3 St. Vincent's Institute of Medical Research and Department of Medicine, University of Melbourne, Fitzroy, Victoria, Australia, the 4 Department of Physiology, Monash University, Clayton, Victoria Australia, the 5 Department of Biochemical Genetics, The Children's Hospital at Westmead, Sydney, New South Wales, Australia, and the 6 Discipline of Genetic Medicine, University of Sydney, New South Wales, AustraliaCorresponding author: Clinton R. Bruce, clinton.bruce@baker.edu.au.Received 5 August 2008 and accepted 2 December 2008.Published ahead of print at http://diabetes.diabetesjournals.org on 10 December 2008. DOI: 10.2337/db08-1078.© 2009 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by -nc-nd/3.0/ for details.The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.,;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号