过氧化物酶体增殖物激活受体的血管生物学:对动脉粥样硬化的调节

The vascular biology of peroxisome proliferator-activated receptors: modulation of atherosclerosis.

作者信息

Verma Subodh, Szmitko Paul E

机构信息

Division of Cardiac Surgery, St. Michael's Hospital, Toronto, Ontario.

出版信息

Can J Cardiol. 2006 Feb;22 Suppl B(Suppl B):12B-17B. doi: 10.1016/s0828-282x(06)70981-3.

Abstract

Accumulating evidence suggests that peroxisome proliferator-activated receptor (PPAR) agonists possess powerful antiatherosclerotic properties, by both directly affecting the vascular wall and indirectly affecting systemic inflammation and insulin sensitivity. The PPARs are ligand-activated transcription factors, which play a number of important physiological roles in lipid and glucose homeostasis. Activation of PPARgamma appears to exert a vasculoprotective effect by limiting endothelial dysfunction, impairing atherogenesis and preventing restenosis, while simultaneously and favourably modulating adipokine expression and lipid metabolism. Several experimental and clinical studies have demonstrated the potential of the PPAR agonist drug class in terms of treating atherosclerotic disease. In the present review, the vascular biology of PPARs, and how the modulation of these molecular pathways may serve as a therapeutic strategy to prevent atherosclerosis, vascular inflammation and restenosis are discussed.

摘要

越来越多的证据表明,过氧化物酶体增殖物激活受体(PPAR)激动剂具有强大的抗动脉粥样硬化特性,这是通过直接影响血管壁以及间接影响全身炎症和胰岛素敏感性来实现的。PPAR是配体激活的转录因子,在脂质和葡萄糖稳态中发挥许多重要的生理作用。激活PPARγ似乎通过限制内皮功能障碍、损害动脉粥样硬化形成和预防再狭窄来发挥血管保护作用,同时有利地调节脂肪因子表达和脂质代谢。多项实验和临床研究已经证明了PPAR激动剂药物类别在治疗动脉粥样硬化疾病方面的潜力。在本综述中,将讨论PPAR的血管生物学,以及这些分子途径的调节如何作为预防动脉粥样硬化、血管炎症和再狭窄的治疗策略。

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