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过氧化物酶体增殖物激活受体γ激动剂与血管危险因素:对心血管疾病的潜在影响

PPARgamma agonists and vascular risk factors: potential effects on cardiovascular disease.

作者信息

Asnani Sunil, Theuma Pierre, Fonseca Vivian A

机构信息

Department of Medicine, Section of Endocrinology, Tulane University Health Sciences Center, New Orleans,Louisiana, USA.

出版信息

Metab Syndr Relat Disord. 2003 Mar;1(1):23-32. doi: 10.1089/154041903321648234.

Abstract

Peroxisome proliferator-activated receptors (PPARs) are members of the nuclear receptor superfamily comprising four subtypes designated PPARalpha, PPARgamma1, PPARgamma2, and PPARdelta. These are transcription factors that regulate gene expression, thereby controlling energy metabolism. PPARgamma has widespread distribution in the adipose tissue, skeletal muscle, heart, liver, kidney, gut, macrophages, and vascular tissues. PPARgamma has a key role in adipogenesis, insulin sensitivity, and glucose and lipid metabolism, and also plays a major role in vascular biology, modulating atherosclerosis progression and vascular endothelial function. Thiazolidinediones (TZDs) are the ligands of PPARgamma, and growing evidence suggests that they might both directly and indirectly influence cardiovascular risk in type 2 diabetes patients by favorably altering several pro-atherogenic metabolic processes.

摘要

过氧化物酶体增殖物激活受体(PPARs)是核受体超家族的成员,包括四种亚型,分别命名为PPARα、PPARγ1、PPARγ2和PPARδ。这些是调节基因表达从而控制能量代谢的转录因子。PPARγ广泛分布于脂肪组织、骨骼肌、心脏、肝脏、肾脏、肠道、巨噬细胞和血管组织中。PPARγ在脂肪生成、胰岛素敏感性以及葡萄糖和脂质代谢中起关键作用,并且在血管生物学中也发挥重要作用,调节动脉粥样硬化进展和血管内皮功能。噻唑烷二酮类(TZDs)是PPARγ的配体,越来越多的证据表明,它们可能通过有利地改变几种促动脉粥样硬化代谢过程,直接和间接影响2型糖尿病患者的心血管风险。

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