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过氧化物酶体增殖物激活受体(PPARs)、心血管代谢与功能:近平衡或远平衡途径。

PPARs, Cardiovascular Metabolism, and Function: Near- or Far-from-Equilibrium Pathways.

机构信息

Service de Physiologie, Hôpital de Bicêtre, Assistance Publique-Hôpitaux de Paris, 94275 Le Kremlin-Bicêtre, France.

出版信息

PPAR Res. 2010;2010. doi: 10.1155/2010/783273. Epub 2010 Jul 27.

DOI:10.1155/2010/783273
PMID:20706650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2913846/
Abstract

Peroxisome proliferator-activated receptors (PPAR alpha, beta/delta and gamma) play a key role in metabolic regulatory processes and gene regulation of cellular metabolism, particularly in the cardiovascular system. Moreover, PPARs have various extra metabolic roles, in circadian rhythms, inflammation and oxidative stress. In this review, we focus mainly on the effects of PPARs on some thermodynamic processes, which can behave either near equilibrium, or far-from-equilibrium. New functions of PPARs are reported in the arrhythmogenic right ventricular cardiomyopathy, a human genetic heart disease. It is now possible to link the genetic desmosomal abnormalitiy to the presence of fat in the right ventricle, partly due to an overexpression of PPARgamma. Moreover, PPARs are directly or indirectly involved in cellular oscillatory processes such as the Wnt-b-catenin pathway, circadian rhythms of arterial blood pressure and cardiac frequency and glycolysis metabolic pathway. Dysfunction of clock genes and PPARgamma may lead to hyperphagia, obesity, metabolic syndrome, myocardial infarction and sudden cardiac death, In pathological conditions, regulatory processes of the cardiovascular system may bifurcate towards new states, such as those encountered in hypertension, type 2 diabetes, and heart failure. Numerous of these oscillatory mechanisms, organized in time and space, behave far from equilibrium and are "dissipative structures".

摘要

过氧化物酶体增殖物激活受体(PPARα、β/δ 和 γ)在代谢调节过程和细胞代谢的基因调控中发挥着关键作用,特别是在心血管系统中。此外,PPAR 还具有多种代谢以外的作用,如昼夜节律、炎症和氧化应激。在这篇综述中,我们主要关注 PPAR 对一些热力学过程的影响,这些过程可以接近平衡,也可以远离平衡。PPAR 的新功能在致心律失常性右心室心肌病中得到了报道,这是一种人类遗传性心脏病。现在可以将基因连接到间隔蛋白异常与右心室脂肪的存在联系起来,部分原因是 PPARγ 的过度表达。此外,PPAR 直接或间接地参与细胞振荡过程,如 Wnt-β-连环蛋白途径、动脉血压和心率的昼夜节律以及糖酵解代谢途径。时钟基因和 PPARγ 的功能障碍可能导致暴饮暴食、肥胖、代谢综合征、心肌梗死和心源性猝死。在病理条件下,心血管系统的调节过程可能会向新的状态分叉,如高血压、2 型糖尿病和心力衰竭中遇到的状态。这些振荡机制中的许多机制,在时间和空间上组织起来,表现出远离平衡的状态,是“耗散结构”。

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