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过氧化物酶体增殖物激活受体 (PPARα/γ) 激动剂作为降低糖尿病患者心血管风险的潜在靶点。

Peroxisome proliferator-activated receptor (PPAR α/γ) agonists as a potential target to reduce cardiovascular risk in diabetes.

机构信息

Cleveland Clinic Coordinating Center for Clinical Research and Department of Cardiovascular Medicine, Cleveland Clinic, OH 44195, USA.

出版信息

Diab Vasc Dis Res. 2012 Apr;9(2):89-94. doi: 10.1177/1479164112441477. Epub 2012 Mar 9.

Abstract

The disappointing results of glucose lowering studies have highlighted the ongoing need to develop new therapeutic strategies to reduce cardiovascular risk in patients with type 2 diabetes. The presence of a range of metabolic abnormalities in diabetic patients presents a number of potential targets for therapeutic intervention. While modulation of peroxisome proliferator activated receptors (PPARs) represents an attractive approach, the results of studies of pharmacological agonists have been variable. The findings of these studies and rationale for development of dual PPAR-α/γ agonists will be reviewed.

摘要

降糖研究令人失望的结果突显了持续开发新的治疗策略以降低 2 型糖尿病患者心血管风险的必要性。糖尿病患者存在多种代谢异常,为治疗干预提供了多个潜在靶点。过氧化物酶体增殖物激活受体(PPAR)的调节是一种有吸引力的方法,但药理学激动剂研究的结果存在差异。本文将回顾这些研究的结果和开发双重 PPAR-α/γ 激动剂的理由。

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