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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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