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糖尿病中新的过氧化物酶体增殖物激活受体激动剂的开发策略。

Strategies for the development of new PPAR agonists in diabetes.

作者信息

Cavender Matthew A, Nicholls Stephen J, Lincoff A Michael

机构信息

Department of Cardiovascular Medicine, The Cleveland Clinic, Cleveland, Ohio 44195, USA.

出版信息

Eur J Cardiovasc Prev Rehabil. 2010 May;17 Suppl 1:S32-7. doi: 10.1097/01.hjr.0000368196.17109.5e.

Abstract

Diabetes is associated with a range of metabolic abnormalities including insulin resistance, atherogenic dyslipidemia, hypertension, and inflammation. These factors are likely to underlie the adverse cardiovascular outcome typically observed in diabetic cohorts. The family of peroxisome proliferator-activated receptors (PPARs) have been implicated in the regulation of a number of physiologic and metabolic pathways. Pharmacologic agonists directed against various PPARs have been shown to have a beneficial impact on these metabolic risk factors. The potential impact on cardiovascular risk with the use of PPAR agonists will be reviewed.

摘要

糖尿病与一系列代谢异常相关,包括胰岛素抵抗、致动脉粥样硬化性血脂异常、高血压和炎症。这些因素可能是糖尿病患者队列中通常观察到的不良心血管结局的潜在原因。过氧化物酶体增殖物激活受体(PPAR)家族参与了许多生理和代谢途径的调节。针对各种PPAR的药物激动剂已被证明对这些代谢危险因素有有益影响。本文将综述使用PPAR激动剂对心血管风险的潜在影响。

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