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依达拉奉对大鼠创伤性脑损伤作用的观察

The experimental study of edaravone injection in rats traumatic brain injury
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摘要 目的:研究依达拉奉超早期应用对创伤性脑损伤继发性损伤(TBI)的保护作用。方法:大鼠随机分为假手术组、生理盐水组(TBI-NS,创伤后30 min、24 h静注生理盐水)、依达拉奉组(TBI-Ed,创伤后30 min、24 h静注依达拉奉)。伤后72 h处死部分大鼠,对伤侧皮层、海马及丘脑进行病理组织学检测。其余大鼠伤后15 d应用Morris水迷宫检测大鼠神经功能,同时监测不同时间活化部分凝血活酶时间(APTT)。结果:依达拉奉组皮层、海马及丘脑坏死神经元计数(F-J染色),水迷宫实验平均上台时间均较生理盐水组显著减少(P<0.05或P<0.01),但APTT与生理盐水组间无显著差异。结论:创伤性脑损伤后,超早期应用依达拉奉能显著减轻神经组织的病理损害,改善实验动物神经功能。 OBJECTIVE To investigate the effect of edaravone injection in the traumatic brain injury(TBI).METHODS Rats were randomly divided into three groups: sham-operation group,saline group(TBI-NS,saline iv,30 min and 24 h post-injury),edaravone group(TBI-Ed,edaravone injection iv,30 min and 24 h post-injury).After 72 h survival,some rats were killed,brain samples(cerebral cortex,hippocampus and thalamus) were harvested for Fluoro-jade staining.Morris water maze was used to detect the neurological outcome after 15 d.APTT was measured in different time point after TBI.RESULTS Compared with saline group,necrosis neurons in cortex,hippocampus CA1 and thalamus area in edaravone group decreased significantly,the mean time on platform of Morris water maze decreased significantly(P0.05 or P0.01).But APTT showed no changes between edaravone and saline group(P0.05).CONCLUSION After brain injury,ultra-early use of edaravone injection could ameliorate pathological lesion and improve neurological outcome.
出处 《中国医院药学杂志》 CAS CSCD 北大核心 2012年第19期1533-1536,共4页 Chinese Journal of Hospital Pharmacy
关键词 创伤性脑损伤 依达拉奉 脑保护 traumatic brain injury edaravone injection cerebral protection
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参考文献8

  • 1Torpy JM, Lynm C, Glass RM. Traumatic brain injury[J]. JAMA, 2003,289(22) ..3038.
  • 2ComPer P, BisschoP SM, Carnide N, et al. A systematic re- view of treatments for mid traumatic brain injury[J]. Brain Inj, 2005,19(1l) :863 880.
  • 3Firuzi O, Miri R, Tavakkoli M, et al. Antioxidant therapy: current status and future prospects[J]. Curr Med Chem, 2011,18 (25) : 3871-3888.
  • 4Bains M, Hall ED. Antioxidant therapies in traumatic brain and spinal cord injury[J]. Biochimica et Biophysica Acta, 2012,1822(5) :675-684.
  • 5Zhang N, Komine-Kobayashi M, Tanaka R, et al. Edaravone reduces early accumulation of oxidative products and sequential inflammatory responses after transient focal isehemia in mice brairt[J]. Strokc,2005,36(10)2220-2225.
  • 6Edaravone Acute Infarction Study Group. Effect of a novel free radical scavenger, edaravone (MCI-186), on acute brain irdare- tion. Randomized, placebo-controlled, double-blind study at multi- eenters[J]. Cerebrovasc Dis, 2003,15(3):222-229.
  • 7Carrick MM, Tyroch AH, Youens CA, et al. Subsequent de- velopment of thrombocytoPenia and coaguloPathy in moderate and severe head injury: suPPort for serial laboratory examina- tion[J]. J Trauma,2005,58(4):725-729.
  • 8Wang GH, Jiang ZL, Li YC, et al. Free-radical scavenger edaravone treatment confers neuroprotection against traumatic brain injury in rats[J]. J Neurotrauma, 2011, 28 (10) .. 2123 2134.

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