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作 者:陈燕启[1] 刘德红[2] 杨光田[2] 姜宏志[1]
机构地区:[1]卫生部北京医院急诊科,北京市100730 [2]华中科技大学同济医学院附属同济医院急诊科
出 处:《中国全科医学》2004年第10期711-712,715,共3页Chinese General Practice
基 金:湖北省科技厅 2 0 0 3年湖北省科技攻关计划 [编号2 0 0 3AA30 1C51 ]
摘 要:目的 观测全脑缺血再灌注时海马CA1区白细胞介素 - 10mRNA (IL - 10mRNA)、肿瘤坏死因子 -αmRNA (TNF -αmRNA)、白细胞介素 - 1βmRNA (IL - 1βmRNA)表达的变化 ,探讨全脑缺血再灌注时IL - 10表达的作用。方法 按照Pullsinelli法建立大鼠全脑缺血再灌注损伤模型 ,分别于缺血再灌注 2、 6、 12、 2 4、 4 8h取脑海马CA1区组织切片 ,用原位杂交法和图像分析检测IL - 10mRNA、TNF -αmRNA、IL - 1βmRNA的吸光度值。结果 脑缺血再灌注各时间点海马CA1区TNF -αmRNA、IL - 1βmRNA的吸光度值均显著增加 (P <0 0 1) ,4 8hIL - 10mRNA显著表达 (P <0 0 1) ;2 4~ 4 8hIL - 10mRNA的吸光度值与TNF -αmRNA、IL - 1βmRNA的吸光度值均呈显著负相关(r值分别为 - 0 70 6、 - 0 84 2 ,P值 <0 0 5 )。结论 大鼠全脑缺血再灌注 4 8hIL - 10显著表达 ,对TNF -α、IL - 1β具有显著的抑制作用。Objective To explore the effect of IL-10,we detected IL-10mRNA and TNF-α mRNA and IL-1βmRNA In rat brain hippocampus CA 1 regions after global cerebral Ischemia-reperfusion.Methods 50 Wistar rats were divided into Sham operation(S)group and ischemia-reperfusion(IR)group.The global cerebral Ischemia-reperfusion animal models were formed by Pullsinelli′s method.The hippocampus CA 1 tissues at 2h,6h,12h,24h,and 48h were taken out respectively after sham operation and global cerebral Ischemia-reperfusion,then the expressions of IL-10mRNA and TNF-α mRNA and IL-1βmRNA were examined by In situ hybridization.Results The changes of all observed targets were as the following:(1) At 48h after global cerebral ischemia-reperfusion,while the expression of IL-10mRNA was Increased significantly (P<0 01),that of TNF-αmRNA and IL-1βmRNA were decreased rapidly.(2) The expressions of TNF-αmRNA and IL-1βmRNA at every time points were Increased significantly (P<0 01),respectively.3 There was negative correlation between IL-10mRNA and TNF-αmRNA and IL-1βmRNA(r=-0706,-0842,P<0 05 or <0 01)respectively.Conclusion The expression of IL-10mRNA,at 48h after global cerebral Ischemia-reperfusion,could reduce obviously expressions of TNF-αmRNA,IL-1βmRNA.
关 键 词:大鼠 全脑缺血再灌注 海马 CA1区 IL-10 实验研究 肿瘤坏死因子
分 类 号:R743.3[医药卫生—神经病学与精神病学]
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