Pharmacodynamic Effect of Ellagic Acid on Ameliorating Cerebral Ischemia/Reperfusion Injury

被引:20
|
作者
Wang, Yeye [2 ,3 ]
Wu, Ying [1 ]
Liang, Chen [3 ]
Tan, Renxiang [4 ]
Tan, Liwei [1 ,2 ]
Tan, Rui [1 ,2 ]
机构
[1] Southwest Jiaotong Univ, Coll Life Sci & Engn, Chengdu 610031, Sichuan, Peoples R China
[2] Southwest Jiaotong Univ, Sch Mat Sci & Engn, Chengdu, Sichuan, Peoples R China
[3] Southwest Jiaotong Univ, Coll Med, Chengdu, Sichuan, Peoples R China
[4] Nanjing Univ Chinese Med, Sch Pharm, Nanjing, Jiangsu, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Tibetan prescriptions; Ellagic acid; Cerebral ischemia; reperfusion injury treatment; Pharmacology; Histopathology; REPERFUSION INJURY; OXIDATIVE STRESS; ISCHEMIC-STROKE; HEART-DISEASE; BLOOD; ANTIOXIDANT; MECHANISMS; INFARCTION; THERAPY; UPDATE;
D O I
10.1159/000502401
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cerebral ischemia/reperfusion (I/R) injury causes a larger population of disable patients and deaths annually. Three Tibetan prescriptions have been applied in alleviating the I/R injury for a 1,000 years. Interestingly, ellagic acid (EA) is one of the commonly dominated phytochemicals in these 3 prescriptions. Therefore, it is noteworthy to evaluate the association between the pharmacodynamics effects of EA and I/R injury alleviation. In this study, we reveal that the EA can effectively reduce the infarction area, and prevent the neuron from apoptosis and damage in permanent middle cerebral artery occlusion rat model. The results of the histopathological study indicate that alleviation of brain damage is positively correlated with the EA dose. Further by biochemical analysis, it indicates that the EA can alleviate the brain damage by the anti-inflammatory and anti-oxidative response mediated by EA. The upregulation of zonula occludens-1 and down-regulation of Aquaporin 4 and matrix metalloprotein 9 (MMP-9) in injured brain tissues after being treated with EA suggested that the reconstruction of brain-blood-barrier (BBB), which can further prevent the brain from further injury by the other xenobiotics. In addition, EA will not activate the coagulation factors XII to induce coagulation formation during the treatment process. Therefore, EA is a promising candidate oral drug for I/R injury therapy.
引用
收藏
页码:320 / 331
页数:12
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