The Protective Effects of Peroxisome Proliferator-Activated Receptor Gamma in Cerebral Ischemia-Reperfusion Injury

被引:43
|
作者
Ding, Yanping [1 ]
Kang, Jie [1 ]
Liu, Shuning [1 ]
Xu, Yuqin [1 ]
Shao, Baoping [2 ]
机构
[1] Northwest Normal Univ, Coll Life Sci, Lanzhou, Peoples R China
[2] Lanzhou Univ, Coll Life Sci, Lanzhou, Peoples R China
来源
FRONTIERS IN NEUROLOGY | 2020年 / 11卷
关键词
cerebral ischemia-reperfusion; peroxisome proliferator-activated receptor γ anti-inflammation; anti-oxidative stress; microglia activation; anti-apoptosis; PROPANE-2-SULFONIC ACID OCTADEC-9-ENYL-AMIDE; BRAIN-BARRIER BREAKDOWN; NF-KAPPA-B; PPAR-GAMMA; OXIDATIVE STRESS; ISCHEMIA/REPERFUSION INJURY; NAD(P)H OXIDASE; DUAL AGONIST; RATS; SUPEROXIDE;
D O I
10.3389/fneur.2020.588516
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cerebral ischemia-reperfusion injury (CI/RI) is a complex pathological process that often occurs secondary to trauma, surgery, and shock. Peroxisome proliferator activated receptor gamma (PPAR gamma) is a subunit of the PPAR and is a ligand-activated nuclear transcription factor. After being activated by its ligand, PPAR gamma can combine with specific DNA response elements to regulate the transcription and expression of genes. It has a wide range of biological functions, such as regulating lipid metabolism, improving insulin sensitivity, modulating anti-tumor mechanisms, and inhibiting inflammation. In recent years, some studies have shown that PPAR gamma exerts a protective effect during CI/RI. This article aims to summarize the research progress of studies that have investigated the protective effects of PPAR gamma in CI/RI and the cellular and molecular mechanisms through which these effects are modulated, including inhibition of excitatory amino acid toxicity, reduced Ca2+ overload, anti-oxidative stress, anti-inflammation, inhibition of microglial activation, maintain the BBB, promotion of angiogenesis, and neurogenesis and anti-apoptotic processes.
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页数:15
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