中国卒中杂志 ›› 2013, Vol. 8 ›› Issue (04): 266-270.

• 论著 • 上一篇    下一篇

酒精对缺血-再灌注大鼠脑组织的保护作用

王彬,刘志辉,张培,李健   

  1. 261031 潍坊
    山东省潍坊医学院附属
    医院神经内科
  • 收稿日期:2012-09-04 出版日期:2013-04-20 发布日期:2013-04-20
  • 通讯作者: 刘志辉 lzhh1957@126.com

Protection of Alcohol to Ischemia-reperfusion Brain Tissue in Rats

  1. Department of Neurology, The Affiliated Hospital of Weifang
    Medical College, Weifang 261031, China
  • Received:2012-09-04 Online:2013-04-20 Published:2013-04-20

摘要:

【摘要】 目的 探讨酒精对缺血-再灌注大鼠脑组织梗死面积、皮质凋亡诱导因子(apoptosis induced factor, AIF)及缺氧诱导因子-1α(hypoxia induced factor-1α,HIF-1α)表达的影响。 方法 将54只健康雄性Wistar大鼠随机分为3组,分别为假手术组、缺血-再灌注组(对照组)、缺 血-再灌注后酒精治疗组(治疗组)。以改良线栓法制成大鼠大脑中动脉闭塞(middle cerebral artery occlusion,MCAO)模型,2 h后拔出线栓,形成缺血-再灌注,治疗组立即腹腔注射1.5 g/kg酒精(无水 酒精稀释成50%酒精),对照组与假手术组腹腔注射等剂量的生理盐水。观察大鼠脑梗死灶面积的 大小,采用免疫组化方法检测大鼠缺血-再灌注脑组织AIF及HIF-1α的表达。 结果 治疗组大鼠脑梗死面积较对照组明显减小[(35.33 6.06)mm2 vs (55.50 3.62)mm2, P <0.001];对照组大鼠脑皮质区AIF及HIF-1α表达分别为(36.75 8.99)个/HP和(49.25 12.04) 个/HP;治疗组大鼠脑皮质区AIF及HIF-1α表达分别为(20.75 7.46)个/HP和(70.25 11.12)个/HP; 治疗组大鼠脑皮质区AIF的表达明显低于对照组(P <0.001),而HIF-1α的表达明显高于对照组 (P <0.001)。 结论 1.5 g/kg酒精对缺血-再灌注大鼠脑组织具有保护作用,可能是通过减少细胞凋亡而减轻脑 损伤。

文章导读: 本研究是国内首次针对酒精可能的脑保护作用进行的动物研究。

关键词: 酒精; 缺血-再灌注; 梗死面积; 凋亡诱导因子; 缺氧诱导因子-1&alpha

Abstract:

【Abstract】 Objective To investigate the influence of alcohol on the infarction area and expression of apoptosis induced factor(AIF), hypoxia induced factor-1α(HIF-1α) in the brain tissue of rats with cerebralreperfusion. Methods Fifty-four healthy male Wistar rats were randomly divided into 3 groups, sham operation group, ischemia-reperfusion group(control group), and ischemia-reperfusion with alcohol group(therapy group). The infarction models were established by blocking the middle cerebral artery, after 2 hours the line was pulled out, forming ischemia-reperfusion in the brain tissue of the rats. Alcohol(absolute alcohol was diluted to 50% alcohol) 1.5 g/kg was intraperitoneally injected to the therapy group when reperfusion, and the control group and sham operation group with the same amount of saline. The infarct size was stained by 2, 3, 5-triphenyltetrazolium chlorice and the expression of AIF and HIF-1α in the brain tissue of the rats was tested by the immunohistochemical method. Results The infarction area in the therapy group was significantly smaller than that in the control group([35.33 6.06]mm2 vs [55.50 3.62]mm2, P <0.001). The expression of AIF and HIF-1α in the brain cortex of rats was (36.75 8.99)/HP and (49.25 12.04)/HP in the control group and (20.75 7.46)/HP and (70.25 11.12)/HP in the therapy group, both of them were higher than the sham operation group(both P <0.001), but the expression of AIF in the brain cortex of rats in the therapy group was significantly lower(P <0.001) and the expression of HIF-1α was significantly higher than the control group(P <0.001).

Conclusion Alcohol(1.5 g/kg) has neuroprotective effects on brain tissue of rats with ischemiareperfusion. In brain ischemia -reperfusion injury, alcohol may reduce the brain damage by the enhancement of nerve cells to adapt the anaerobic environment and reducing apoptosis of the nerve cells.

Key words: Alcohol; Cerebral-reperfusion; Infarct area; Apoptosis induced factor; Hypoxia induced factor-1α