Effects of Electroacupuncture on Cerebro-cortical Catalase,GSH-Px and Total Anti-oxidation Capability in Focal Cerebral Ischemia-reperfusion Rats
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Effects of Electroacupuncture on Cerebro-cortical Catalase,GSH-Px and Total Anti-oxidation Capability in Focal Cerebral Ischemia-reperfusion Rats
Acupuncture ResearchIssue 6, Pages: 377-379(2007)
作者机构:
1. 陕西中医学院
2. 陕西中医学院,咸阳,712083
3. ,咸阳,712083
作者简介:
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Published:2007
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NIU Wen-min, LIU Zhi-bin. Effects of Electroacupuncture on Cerebro-cortical Catalase,GSH-Px and Total Anti-oxidation Capability in Focal Cerebral Ischemia-reperfusion Rats[J]. Acupuncture research, 2007, (6): 377-379.
DOI:
NIU Wen-min, LIU Zhi-bin. Effects of Electroacupuncture on Cerebro-cortical Catalase,GSH-Px and Total Anti-oxidation Capability in Focal Cerebral Ischemia-reperfusion Rats[J]. Acupuncture research, 2007, (6): 377-379.DOI:
Effects of Electroacupuncture on Cerebro-cortical Catalase,GSH-Px and Total Anti-oxidation Capability in Focal Cerebral Ischemia-reperfusion Rats
Objective:To observe the effect of electroacupuncture(EA)of "Xiusanzhen" on anti-oxidation in cerebral ischemia-reperfusion(CI-R)injury rats and to analyze its underlying mechanism in resisting cerebral ischemic injury.Methods:A total of 30 SD rats were randomized into sham
model and EA groups
with 10 cases in each.CI-R model was established by reversible occlusion of the middle cerebral artery.EA(80-100 Hz
1-3 mA)was applied to "Xiusanzhen"(the mid-point of the nasal root
2 mm bilateral to the nasal root)for 60 min.The levels of catalase(CAT)
glutathione peroxidase(GSH-Px)and total anti-oxidation capability(T-AOC)in cerebral cortex tissue were determined by using spectrophotometry and chromatometry respectively.Results:Compared with control group
the levels of CAT
GSH-Px and T-AOC in model group were markedly lower(P<0.01);while compared with model group
the levels of CAT
GSH-Px and T-AOC increased significantly in EA group(P<0.01).Conclusion:EA of "Xiusanzhen" has definite effects in raising CI-R-induced decrease of CAT
GSH-Px activity and T-AOC in the cerebral cortex
which may contribute to its effect in reducing ischemic cerebral damage.