Chinese medicine Nao-Shuan-Tong attenuates cerebral ischemic injury by inhibiting apoptosis in a rat model of stroke

被引:30
作者
Xiang, Jun [1 ]
Tang, Yu-Ping [1 ]
Wu, Ping [1 ]
Gao, Jun-Peng [1 ]
Cai, Ding-Fang [1 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Inst Integrat Med, Lab Neurol, Shanghai 200032, Peoples R China
关键词
Nao-Shuan-Tong; Cerebral ischemia; Apoptosis; Caspases; Bax/Bcl-2; KOREAN HERBAL FORMULATION; CELL-DEATH; ARTERY OCCLUSION; MECHANISMS; BRAIN; SILSOSANGAMI; HIPPOCAMPUS; INFARCTION; EVOLUTION; PENUMBRA;
D O I
10.1016/j.jep.2010.06.021
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Nao-Shuan-Tong (NST) in capsule form is a compound prescription formulated according to the meridian theory of traditional Chinese medicine (TCM) and is approved by the State Food and Drug Administration of China for the treatment of ischemic stroke. Objectives: To test the neuroprotective effects of the Chinese medicine Nao-Shuang-Tong on cerebral ischemia in rats and to explore the underlying mechanisms. Materials and methods: 115 Male Sprague-Dawley rats were randomly divided into 5 groups: sham, ischemia-reperfusion (I/R), and I/R plus NST 0.25, NST 0.5 and NST 1 (n = 23 in each group). Cerebral ischemia was induced by 1.5 h of middle cerebral artery occlusion. Cerebral infarct area was measured by tetrazolium staining at 24 h following reperfusion, and neurological functional deficits were assessed at 1, 3,7 and 14 d after reperfusion. Neuronal apoptosis was studied by Nissl staining and DNA fragmentation assay at 1 and 3d after reperfusion. The activation of caspase-3, -8. -9 and Bax/Bcl-2 levels were analyzed by western blot 24 h after reperfusion. Results: NST (0.5 and 1 g/kg) significantly reduced cerebral infarct area, attenuated neurological functional deficits, and reduced neuronal apoptosis in ischemic cortex and in the CM region of hippocampus. NST also suppressed overexpression of Bax and activated caspases-3, -8 and -9, and also inhibited the reduction of Bcl-2 expression and markedly depressed the Bax/Bcl-2 ratio. Conclusions: These findings demonstrate that NST is neuroprotective against cerebral ischemia and is likely to act via inhibition of neuronal apoptosis associated with changes in levels of caspases-3 and -8. Bax and Bcl-2. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:174 / 181
页数:8
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