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去铁敏预处理对大鼠星型胶质细胞缺氧性损伤的保护作用
引用本文:李云霞,丁素菊,詹青,肖林,郭卫.去铁敏预处理对大鼠星型胶质细胞缺氧性损伤的保护作用[J].第二军医大学学报,2010,31(2):144-147.
作者姓名:李云霞  丁素菊  詹青  肖林  郭卫
作者单位:1. 第二军医大学长海医院神经内科,上海200433;同济大学附属同济医院神经内科,上海200065
2. 第二军医大学长海医院神经内科,上海,200433
3. 同济大学附属同济医院神经内科,上海,200065
4. 第二军医大学基础部神经生物研究所,上海,200433
基金项目:国家自然科学基金(30170340)~~
摘    要:目的探讨去铁敏预处理对星型胶质细胞(AS)缺氧损伤的保护作用及可能机制。方法体外培养AS,建立去铁敏糖氧剥夺(OGD)模型,细胞分为:正常培养组、去铁敏预处理组(先给予去铁敏预处理,再给予去铁敏OGD)、OGD组(给予去铁敏OGD)。采用细胞活力测定、细胞核固缩比率、形态学改变评价去铁敏预处理后的保护效应。用免疫荧光染色检测去铁敏预处理后AS的缺氧诱导因子-1α(HIF-1α)和促红细胞生成素(EPO)蛋白表达情况,RT-PCR检测HIF-1α和EPO的mRNA变化情况。结果去铁敏预处理组细胞形态保持良好,AS活力下降减轻为58%(OGD组25%,P<0.05),细胞核固缩百分比为38%(OGD组30%,P<0.05)。免疫荧光染色发现,体外培养的AS在预处理后出现HIF-1α和EPO蛋白表达。RT-PCR发现去铁敏化学缺氧能上调HIF-1α及EPO mRNA表达。结论去铁敏预处理有确切有效的抗缺氧损伤作用,这种效应与保护AS有关,其机制可能是去铁敏诱导了HIF-1α和EPO表达增加。

关 键 词:去铁敏  缺血预处理  缺氧诱导因子1α  红细胞生成素  
收稿时间:2009/7/20 0:00:00
修稿时间:2009/12/14 0:00:00

Deferoxamine preconditioning protects against hypoxia injury in astrocytes
LI Yun-xi,DING Su-ju,ZHAN Qing,XIAO Lin,GUO Wei.Deferoxamine preconditioning protects against hypoxia injury in astrocytes[J].Academic Journal of Second Military Medical University,2010,31(2):144-147.
Authors:LI Yun-xi  DING Su-ju  ZHAN Qing  XIAO Lin  GUO Wei
Institution:1. Departmeent of Neurology, Changhai Hospital, Second Military Medical University,Shanghai 200433, China;2. Department of Neurology, Tongji Hospital,Tongji University, Shanghai 200065, China ;3. Institute of Neurology, College of Basic Medical Sciences, Second Military Medical University, Shanghai 200433, China
Abstract:Objective To investigate the protective effect of deferoxamine preconditioning against hypoxia injury in astrocytes and the underlying mechanisms.Methods Astrocytes were cultured under ischemia stress,which was mimicked by oxygen and glucose deprivation(OGD) with deferoxamine.Astrocytes were divided into three groups: normally cultured group;Deferoxamine pretreated group: astrocytes were pretreated with Deferoxamine and then treated with Deferoxamine OGD;and OGD group;astrocytes were treated with Deferoxami...
Keywords:deferoxamine  ischemic preconditioning  hypoxia-inducible factor 1 alpha  erythropoietin  
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