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过氧化物酶体增殖物激活受体 δ 的神经保护机制:氧化应激和炎症过程的调节。

Neuroprotective Mechanisms of PPARδ: Modulation of Oxidative Stress and Inflammatory Processes.

机构信息

Department of Cancer Biology, Comprehensive Cancer Center, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.

出版信息

PPAR Res. 2011;2011:373560. doi: 10.1155/2011/373560. Epub 2011 Oct 29.

Abstract

Peroxisome proliferator-activated receptors (PPARα, δ, and γ) are ligand-activated transcription factors that regulate a wide range of cellular processes, including inflammation, proliferation, differentiation, metabolism, and energy homeostasis. All three PPAR subtypes have been identified in the central nervous system (CNS) of rodents. While PPARα and PPARγ are expressed in more restricted areas of the CNS, PPARδ is ubiquitously expressed and is the predominant subtype. Although data regarding PPARδ are limited, studies have demonstrated that administration of PPARδ agonists confers neuroprotection following various acute and chronic injuries to the CNS, such as stroke, multiple sclerosis, and Alzheimer's disease. The antioxidant and anti-inflammatory properties of PPARδ agonists are thought to underly their neuroprotective efficacy. This review will focus on the putative neuroprotective benefits of therapeutically targeting PPARδ in the CNS, and specifically, highlight the antioxidant and anti-inflammatory functions of PPARδ agonists.

摘要

过氧化物酶体增殖物激活受体 (PPARα、δ 和 γ) 是配体激活的转录因子,可调节多种细胞过程,包括炎症、增殖、分化、代谢和能量稳态。这三种 PPAR 亚型在啮齿动物的中枢神经系统 (CNS) 中均有发现。虽然 PPARα 和 PPARγ 在 CNS 的限定区域表达,但 PPARδ 广泛表达,是主要的亚型。尽管关于 PPARδ 的数据有限,但研究表明,在中枢神经系统受到各种急性和慢性损伤(如中风、多发性硬化症和阿尔茨海默病)后,给予 PPARδ 激动剂可提供神经保护作用。PPARδ 激动剂的抗氧化和抗炎特性被认为是其神经保护作用的基础。这篇综述将重点介绍在中枢神经系统中靶向治疗 PPARδ 的潜在神经保护益处,并特别强调 PPARδ 激动剂的抗氧化和抗炎功能。

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