神经药理学报››2011,Vol. 1››Issue (2): 7-13.

• 研究论文 •上一篇下一篇

大黄酚脂质体对脑缺血再灌注损伤小鼠海马神经元凋亡的影响

宋金艳, 张  力, 赵晓倩, 宋志斌

  1. 欧宝平台登录 药理教研室,张家口,075000,中国
  • 出版日期:2011-04-26发布日期:2012-04-20
  • 通讯作者:张力,男,教授,硕士生导师;研究方向:神经药理学;Tel:+86-0313-4029188,E-mail:zmczl@hotmail.com
  • 作者简介:宋金艳,女,河北廊坊人,硕士研究生;E-mail:songjy1008@163.com
  • 基金资助:

    河北省自然科学基金资助项目(No.C2009001026)

Effects of Chrysophanol Liposomes on Apoptosis of the Hippocampal Neurons in Mice after Cerebral Ischemia and Reperfusion Injury

SONG Jin-yan,ZHANG Li,ZHAO Xiao-qian,SONG Zhi-bin

  1. Department of Pharmacy,Hebei North University,Zhangjiakou,075000,China
  • Online:2011-04-26Published:2012-04-20

摘要:目的:观察脑缺血再灌注损伤后,大黄酚脂质体对小鼠海马神经元凋亡的影响,探讨大黄酚脂质体对脑缺血再灌注损伤小鼠海马的保护作用及其机制。方法: 采用暂时性阻断颈总动脉的方法建立小鼠脑缺血再灌注损伤模型,腹腔注射(ip)大黄酚脂质体 10.0,1.0,0.1 mg· kg-1,观察小鼠脑缺血再灌注后神经功能学和病理形态学的改变,并采用免疫组化方法检测海马神经元凋亡相关蛋白半胱氨酰天冬氨酸蛋白酶 -3(caspase-3),Bcl-2和 Bcl-2-Associated X(Bax)的表达。结果: 大黄酚脂质体可明显抑制脑缺血再灌注引起的神经元的丢失,提高 Bcl-2 的表达,降低 caspase-3 和 Bax 的表达,提高神经功能评分,减少病理形态改变,减轻海马神经元损伤,其中以 10.0 mg· kg-1组大黄酚脂质体的作用最为明显(P<0.05)。结论: 脑缺血再灌注损伤后应用大黄酚脂质体对海马神经元有明显的保护作用,其机制可能与上调 Bcl-2 的表达,下调 caspase-3 和 Bax 的表达有关。

关键词:大黄酚脂质体,脑缺血再灌注损伤,海马,凋亡,caspase-3 ,Bcl-2 ,Bax

Abstract:Objective:To observe the influence of chrysophanol liposomes on apoptosis of hippocampal neurons in mice and to study the protective effects on cerebral ischemia and reperfusion injury and its mechanism.Methods:Cerebral ischemia and reperfusion injury was produced in conscious mice by temporarily obstructing bilateral common carotid arteries. Chrysophanol liposomes(10.0,1.0,0.1 mg· kg-1)was injected intraperitoneally. The effects of chrysophanol liposomes were studied on the neurological function, the pathomorphology of brain tissues and the expression of apoptosisrelated protein caspase-3, Bcl-2 and Bax in hippocampal neuron using immunohistochemistry.Results: Chrysophanol liposomes could increase the expression of Bcl-2, decrease the expression of Bax and caspase-3, improve the neurological function score and decrease the pathological change in chrysophanol liposomes treated animals. The effect of chrysophanol liposomes was most obviously in group 10.0 mg· kg-1P<0.05).Conclusion: Chrysophanol liposomes have a significant protective effect on hippocampal neurons after cerebral ischemia and reperfusion injury. The mechanism may be related to increasing the expression of Bcl-2, reducing caspase-3 and Bax.

Key words:chrysophanol liposomes,cerebral ischemia and reperfusion injury,hippocampal,apoptosis,caspase-3,Bcl-2,Bax

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