节点文献

PPARs与心血管疾病

PPARs and Cardiovascular Disease

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 付燕王嘉陵向继洲

【Author】 FU Yan,WANG Jialing,XIANG Jizhou Department of Pharmacology,School of Basic Medical Sciences,Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030,China

【机构】 华中科技大学同济医学院药理学系华中科技大学同济医学院药理学系 武汉市430030武汉市430030

【摘要】 PPAR是核受体超家族成员之一 ,它可以促进脂肪细胞分化 ,在脂质代谢中起着重要的作用。随着对胰岛素增敏剂尤其是噻唑烷二酮类 (TZDs)药物作用机制的深入研究 ,人们发现PPAR就是这类药物的主要作用靶点。PPAR不仅与胰岛素抵抗关系密切 ,在动脉粥样硬化、高血压、心肌肥厚和心肌炎的发生、发展及防治过程中也起着重要的作用。进一步探讨PPAR与心血管疾病的关系 ,可能为TZDs类药物治疗糖尿病心血管并发症提供新的理论基础 ,也可能为心血管药物治疗提供新的治疗靶点。

【Abstract】 Peroxisome proliferator-activated receptors (PPARs) were classified as orphan members of the nuclear receptor superfamily. It may induce adipocyte differentiation and regulate the metabolism of lipids. Recently, with further study of the mechanism of insulin sensitizer such as TZDs, it has been realized that PPARs are the main target of these drugs. PPARs not only are linked to insulin resistance, but play an important role in the development of human cardiovascular diseases such as atherosclerosis, hypertension, cardiac hypertrophy and myocarditis. This article reviews the relationship between PPARs and cardiovascular diseases, in order to provide important insight into the roles of TZDs in treating diabetic complications and find new targets of cardiovascular drugs in the future.

【关键词】 PPAR噻唑烷二酮类心血管疾病
【Key words】 PPARTZDscardiovascular desease
【基金】 国家自然科学基金 (No .3 0 17115 1)
  • 【文献出处】 医学分子生物学杂志 ,Foreign Medical Sciences , 编辑部邮箱 ,2004年06期
  • 【分类号】R54
  • 【被引频次】6
  • 【下载频次】343
节点文献中: 

本文链接的文献网络图示:

本文的引文网络