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参芪扶正注射液对老年大鼠脑缺血/再灌注损伤的保护作用

[Protective effect of shenqi fuzheng injection on cerebral ischemia/reperfusion injured aged rats].

作者信息

Cai Ying-min, Hu Hai-tao, Ma Xiao-ya

机构信息

Department of Anesthesia, The Second Affiliated Hospital, Xi' an Jiao-tong University, Xi' an (710004).

出版信息

Zhongguo Zhong Xi Yi Jie He Za Zhi. 2006 Jun;26 Suppl:10-4.

Abstract

OBJECTIVE

To study the protective effects of Shenqi Fuzheng Injection (SFI) on cerebral ischemia/reperfusion injured aged rats.

METHODS

Aged SD male rats, weighing 200-300 g, were randomly divided into 4 groups: the model group, the sham-operative group, the nimodipine positive control group (abbreviated as nimodipine group) and the SFI group. Focal cerebral ischemia/reperfusion injured rat model was established by modified Longa method. SFI was administered by intravenous dripping 1 week before ischemia. Nervous function disorder, brain infarction area, serum lactate dehydrogenase (LDH) and creatine kinase (CK) levels, brain contents of Ca2+ , water, MDA and SOD levels were observed 3 hrs after ischemia and 3 hrs after reperfusion.

RESULTS

perimental results showed that SFI could obviously improve the deficit of nerve function, decrease water content of brain, reduce the infarction area of brain, and inhibit Ca2 + aggregation. LDH and CK levels in serum and MDA in brain were obviously lower than those in the model group and SOD activity in cerebral tissue was obviously higher than that in the model group.

CONCLUSION

SFI had protective effect on cerebral ischemia/reperfusion injured aged rats, whose mechanism might be related to the inhibition of lipid peroxidation and Ca2+ aggregation.

摘要

目的

研究参芪扶正注射液(SFI)对脑缺血/再灌注损伤老龄大鼠的保护作用。

方法

选取体重200 - 300 g的雄性老龄SD大鼠,随机分为4组:模型组、假手术组、尼莫地平阳性对照组(简称尼莫地平组)和SFI组。采用改良Longa法建立局灶性脑缺血/再灌注损伤大鼠模型。在缺血前1周通过静脉滴注给予SFI。观察缺血3小时后及再灌注3小时后的神经功能障碍、脑梗死面积、血清乳酸脱氢酶(LDH)和肌酸激酶(CK)水平、脑内Ca2+、水、丙二醛(MDA)含量及超氧化物歧化酶(SOD)水平。

结果

实验结果表明,SFI可明显改善神经功能缺损,降低脑含水量,缩小脑梗死面积,并抑制Ca2+聚集。血清中LDH和CK水平以及脑内MDA含量明显低于模型组,脑组织中SOD活性明显高于模型组。

结论

SFI对脑缺血/再灌注损伤老龄大鼠具有保护作用,其机制可能与抑制脂质过氧化和Ca2+聚集有关。

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