Curcumin Protects Neurons Against Oxygen-Glucose Deprivation/Reoxygenation-Induced Injury Through Activation of Peroxisome Proliferator-Activated Receptor-c Function

被引:25
|
作者
Liu, Zun-Jing [1 ]
Liu, Hong-Qiang [2 ]
Xiao, Cheng [3 ]
Fan, Hui-Zhen [4 ]
Huang, Qing [5 ]
Liu, Yun-Hai [5 ]
Wang, Yu [1 ]
机构
[1] China Japan Friendship Hosp, Dept Neurol, Beijing 100029, Peoples R China
[2] Jining 1 Peoples Hosp, Dept Pharm, Jining, Peoples R China
[3] China Japan Friendship Hosp, Inst Clin Med, Beijing 100029, Peoples R China
[4] Peoples Hosp Yichun City, Dept Gastroenterol, Yichun, Peoples R China
[5] Cent S Univ, Dept Neurol, Xiangya Hosp, Changsha, Hunan, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
oxygen-glucose deprivation; mitochondria; peroxisome proliferator-activated receptor gamma; curcumin; nuclear factor-kappa B; BCL-2 FAMILY PROTEINS; KAPPA-B ACTIVATION; PPAR-GAMMA; CEREBRAL-ISCHEMIA; OXIDATIVE STRESS; MECHANISMS; APOPTOSIS; BRAIN; ROSIGLITAZONE; SUMOYLATION;
D O I
10.1002/jnr.23438
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The turmeric derivative curcumin protects against cerebral ischemic injury. We previously demonstrated that curcumin activates peroxisome proliferator-activated receptor-gamma (PPAR gamma), a ligand-activated transcription factor involved in both neuroprotective and anti-inflammatory signaling pathways. This study tested whether the neuroprotective effects of curcumin against oxygen-glucose deprivation/reoxygenation (OGD/R)-induced injury of rat cortical neurons are mediated (at least in part) by PPAR gamma. Curcumin (10 mu M) potently enhanced PPAR gamma expression and transcriptional activity following OGD/R. In addition, curcumin markedly increased neuronal viability, as evidenced by decreased lactate dehydrogenase release and reduced nitric oxide production, caspase-3 activity, and apoptosis. These protective effects were suppressed by coadministration of the PPAR gamma antagonist 2-chloro-5-nitrobenzanilide (GW9662) and by prior transfection of a small-interfering RNA (siRNA) targeting PPAR gamma, treatments that had no toxic effects on healthy neurons. Curcumin reduced OGD/R-induced accumulation of reactive oxygen species and inhibited the mitochondrial apoptosis pathway, as indicated by reduced release of cytochrome c and apoptosis-inducing factor and maintenance of both the mitochondrial membrane potential and the Bax/Bcl-2 ratio. Again, GW9662 or PPAR gamma siRNA transfection mitigated the protective effects of curcumin on mitochondrial function. Curcumin suppressed I kappa B kinase phosphorylation and I kappa B degradation, thereby inhibiting nuclear factor-kappa B (NF-kappa B) nuclear translocation, effects also blocked by GW9662 or PPAR gamma siRNA. Immunoprecipitation experiments revealed that PPAR gamma interacted with NF-kappa B p65 and inhibited NF-kappa B activation. The present study provides strong evidence that at least some of the neuroprotective effects of curcumin against OGD/R are mediated by PPAR gamma activation. (C) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:1549 / 1559
页数:11
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