Curcumin Prevents Cerebral Ischemia Reperfusion Injury Via Increase of Mitochondrial Biogenesis

被引:103
作者
Liu, Li [1 ,2 ]
Zhang, Wenchao [1 ]
Wang, Li [3 ]
Li, Yu [4 ,5 ]
Tan, Botao [6 ]
Lu, Xi [1 ]
Deng, Yushuang [1 ]
Zhang, Yuping [1 ]
Guo, Xiuming [1 ]
Mu, Jun [1 ]
Yu, Gang [1 ]
机构
[1] Chongqing Med Univ, Dept Neurol, Affiliated Hosp 1, Chongqing 400016, Peoples R China
[2] Chongqing Hosp Tradit Chinese Med, Dept Brain, Chongqing 400021, Peoples R China
[3] Chongqing Canc Inst, Chongqing 400010, Peoples R China
[4] Chongqing Med Univ, Dept Pathol, Chongqing 400016, Peoples R China
[5] Chongqing Med Univ, Inst Neurosci, Chongqing 400016, Peoples R China
[6] Chongqing Med Univ, Dept Rehabil, Affiliated Hosp 2, Chongqing 400010, Peoples R China
基金
美国国家科学基金会;
关键词
Cerebral ischemia reperfusion; Curcumin; Mitochondrial biogenesis; HIPPOCAMPAL CA1 SUBFIELD; GAMMA COACTIVATOR-1-ALPHA; UNCOUPLING PROTEIN-2; OXIDATIVE STRESS; ARTERY OCCLUSION; PGC-1-ALPHA; PROTECTS; DAMAGE; ISCHEMIA/REPERFUSION; ACTIVATION;
D O I
10.1007/s11064-014-1315-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Curcumin is known to have neuroprotective properties in cerebral ischemia reperfusion (I/R) injury. However, the underlying molecular mechanisms remain largely unknown. Recently, emerging evidences suggested that increased mitochondrial biogenesis enabled preventing I/R injury. Here, we sought to determinate whether curcumin alleviates I/R damage through regulation of mitochondrial biogenesis. Sprague-Dawley rats were subjected to a 2-h period of right middle cerebral artery occlusion followed by 24 h of reperfusion. Prior to onset of occlusion, rats had been pretreated with either low (50 mg/kg, intraperitoneal injection) or high (100 mg/kg, intraperitoneal injection) dose of curcumin for 5 days. Consequently, we found that curcumin pretreatment enabled improving neurological deficit, diminishing infarct volume and increasing the number of NeuN-labeled neurons in the I/R rats. Accordingly, the index of mitochondrial biogenesis including nuclear respiratory factor-1, mitochondrial transcription factor A and mitochondrial number significantly down-regulated in I/R rats were reversed by curcumin pretreatment in a dose-dependent manner, and the mitochondrial uncoupling protein 2 presented the similar change. Taken together, our findings provided novel evidence that curcumin may exert neuroprotective effects by increasing mitochondrial biogenesis.
引用
收藏
页码:1322 / 1331
页数:10
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