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诱导大鼠产生脑缺血耐受的时间剂量探讨 被引量:8

Exploration of Ischemic Preconditioning Time for Inducing Rat Brain Ischemia Tolerance
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摘要 目的探讨诱导大鼠脑缺血耐受产生的缺血预处理时间剂量。方法采用前脑-局灶脑缺血耐受模型,短暂性阻断双侧颈总动脉造成前脑缺血预处理,72h后行最后一次局灶性脑缺血2h(中动脉栓塞,MCAO),脑缺血预处理时间剂量分别为10min、20min,通过测定脑梗死面积百分率,探讨诱导大鼠脑缺血耐受产生的最佳缺血预处理时间剂量。结果10min和20min短暂的脑缺血预处理均可以保护大脑抵御下次严重的缺血,使缺血梗死面积显著缩小;10min缺血预处理时间组和20min缺血预处理时间组相比没有显著性差异,但10min缺血预处理时间组脑梗死面积百分率小于20min缺血预处理时间组。结论10min缺血预处理时间是较好的诱导脑缺血耐受产生的时间剂量。 Objective To investigate the ischemic preconditioning time for inducing rat brain ischemia tolerance. Methods Procerebrum ischemie preconditioning injury was caused by occlusion of two- side common carotid artery for 10 minutes or 20 minutes, and subsequent cerebral ischemic injury was caused by occlusion of middle cerebral artery for 2 hours after 72 hours of reperfusion. The percentage of brain infarct size was calculated for the investigation of the proper ischemic preconditioning time for rat brain isehemia tolerance. Results Ischemic preconditionaing for 10 minutes and 20 minutes can reduce the percentage of brain infarct size significantly. The difference of the percentage of brain infarct size between 10 - minute preconditioning group and 20 - minute preconditioning group is insignificant, but the mean percentage of brain infarct size in 10 - minute preconditioning group is less than that in 20 - minute preconditioning group. Conclusion Ten minutes are the suitable time of ischemic preconditioning for rat brain isehemia tolerance.
出处 《中药新药与临床药理》 CAS CSCD 北大核心 2009年第6期585-587,共3页 Traditional Chinese Drug Research and Clinical Pharmacology
基金 河南省重大公益性科研计划[豫财办教(2007)264号]
关键词 脑缺血 缺血预处理 时间剂量 梗死面积 Cerebral ischemia Ischemic preconditioning Time dose Brain infarct size
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参考文献9

  • 1Kitagawa K, Matsumoto M, Tagaya M, et al. Ischemic tolerance phenomenon found in the brain[J]. Brain Res, 1990, 528(1) : 21 -24.
  • 2Koizumi J, Yoshida Y, Nakazawa T, et al. Experimental studies of ischemia brain edema, Ⅰ : A new experimental model of cerebral embolism in rats in which recirculation can be introduced in the ischemic area[J].JpnJStroke, 1986: 8: 1-8.
  • 3Nagasawa H, Kogure K. Correlation between cerebral blood flow and histologic changes in a new rat model of middle cerebral artery occlusion[J]. Stroke, 1989, 20(8) : 1037 - 1043.
  • 4Longa EZ, Weinstein PR, Carlson S, et al. Reversible middle cerebral artery occlusion[J].Stroke, 1989, 20: 84-91.
  • 5Glazier SS, O' Rourke DM, Graham DI, et al. Induction of ischemic tolerance following brief focal ischemia in rat brain[J] . Cereb Blood Flow Metab, 1994, 14(3): 545-553.
  • 6Simon RP, Niiro M, Gwinn R. Prior ischemic stress protects against experimental stroke[J]. Neurosci Lett, 1995, 163(1) : 135 - 137.
  • 7巴晓红 ,巴彩凤 ,李艳君 .脑缺血耐受机制及脑缺血预处理的研究进展[J].中国康复医学杂志,2005,20(9):718-720. 被引量:4
  • 8邓艳秋,赵纲,王建枝.脑缺血预处理与脑缺血耐受的研究进展[J].临床神经病学杂志,2005,18(2):155-156. 被引量:7
  • 9Masads T, Hua Y, Xi G, et al. attenuation of ischemic brain edema and cerebrovaseular injury after ischemic preconditioning in the rat[J]. Cerebral Blood Flow Meta, 2001, 21 ( 1 ) : 22 - 23.

二级参考文献46

  • 1Ishida A,Kawakami H,Yasuzumi F,et al.No To Shinkei,2002,54: 213.
  • 2Wu C,Zhan RZ,Qi S,et al.J Neurosci Methods,2001,107:101.
  • 3Welsh FA.Nippon Ika Daigaku Zasshi,1998,65:447.
  • 4Xiong L,Zheng Y,Wu M,et al.Anesth Analg,2003,96:233.
  • 5Reshef A,Sperling O,Zoref-Shani E.Neurosci Lett,1998,250:111.
  • 6Belayev L,Ginsberg MD,Alonso OF,et al.Neuroreport,1996,8:55.
  • 7Ogita K,Mitani A,Zhang L,et al.Brain Res,2000,872:282.
  • 8Herrera DG,Robertson HA.Prog Neurobiol,1996,50:83.
  • 9Blondeau N,Widmann C,Lazdunski M,et al.J Neurosci,2001,21:4668.
  • 10Kato H,Kogure K,Nakata N,et al.Brain Res Bull,1995,36:205.

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