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过氧化物酶体增殖物激活受体作为调节与代谢综合征相关的心血管危险因素的靶点。

PPARs as targets for the modulation of cardiovascular risk factors associated with the metabolic syndrome.

作者信息

Fernandez Ana Z

机构信息

Laboratorio de Trombosis Experimental, Centro de Biofisica y Bioquimica, IVIC, Apdo 21827, Caracas 1020, Venezuela.

出版信息

Curr Opin Investig Drugs. 2004 Sep;5(9):936-40.

Abstract

Peroxisome proliferator-activated receptor (PPAR) agonists have long been used for the treatment of diabetes and hypercholesterolemia--disorders that give individuals a high predisposition for cardiovascular disease. Prevention of the onset of the latter can begin when a diagnosis of metabolic syndrome, a pathology that groups glucose and lipid disturbances, is made. Although the characteristic components of metabolic syndrome (ie, high blood pressure, obesity, dyslipidemia, insulin resistance and proinflammatory state) are likely to improve through a radical change in lifestyle, a therapeutic approach is also advisable, and the PPAR agonists are the first in a growing list of drugs that may be effective in the prevention of the development of cardiovascular disease.

摘要

过氧化物酶体增殖物激活受体(PPAR)激动剂长期以来一直用于治疗糖尿病和高胆固醇血症,这些疾病使个体极易患心血管疾病。当诊断出代谢综合征(一种将葡萄糖和脂质紊乱归为一组的病症)时,就可以开始预防心血管疾病的发作。虽然代谢综合征的典型组成部分(即高血压、肥胖、血脂异常、胰岛素抵抗和促炎状态)可能通过生活方式的彻底改变而得到改善,但采用治疗方法也是可取的,PPAR激动剂是越来越多可能有效预防心血管疾病发展的药物中的首选。

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