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低温联合褪黑素降低小鼠局灶性脑缺血再灌注损伤

陈武 李毅 段发兰 李国玲 陈琴华 张正洪

湖北医药学院学报2017,Vol.36Issue(1):1-5,封2,6.
湖北医药学院学报2017,Vol.36Issue(1):1-5,封2,6.DOI:10.13819/j.issn.1006-9674.2017.01.001

低温联合褪黑素降低小鼠局灶性脑缺血再灌注损伤

Hypothermia Combined with Melatonin Decreases Reperfusion Injuries of Mouse Focal Cerebral Ischemia

陈武 1李毅 1段发兰 1李国玲 1陈琴华 2张正洪3

作者信息

  • 1. 湖北医药学院附属东风医院检验部,湖北十堰442008
  • 2. 湖北医药学院附属东风医院实验中心,湖北十堰442008
  • 3. 湖北医药学院附属东风医院神经内科,湖北十堰442008
  • 折叠

摘要

Abstract

Objective To explore the protective effects of physical hypothermia (PH) combined with melatonin (MLT) on cerebral ischemia-reperfusion injuries.Methods An in vitro oxidative stress model of mouse primary cortical neuron (PCN) was prepared using hydrogen peroxide (H2O2),and a mouse model of middle cerebral artery occlusion-reperfusion was prepared using suture embolization method.Both cellar and animal model studies included PH (34 ℃) group,melatonin group,PH (34 ℃) plus melatonin group.The protective effect on PCN was evaluated by 4',6-diamidino-2-phenylindole (DAPI) staining and lactate dehydrogenase (LDH) activity assay,and MCAO-reperfused animals were evaluated by 2,3,5-triphenyltetrazolium chloride (TTC) staining and neurological behavior scoring.Results The relative LDH activities of PCN in H2O2,PH,MLT,PH plus MLT groups were 172.8%±12.1%,150.3%±4.36%,141.6%±9.3% and 117.2%±8.2% respectively,which had significant difference from each other (F=33.10,P=0.000).In comparison with vehicle group,the relative brain infarct volumes of HT,MLT and combination groups were decreased by 14.7%,26.8%,56.9%,respectively.The neurobehavioral scoring of three treatment groups were also better than vehicle group.Conclusion The present results indicated that both HT and MLT pretreatment had protective effects on ischemia-reperfusion brain injuries.While combining HT with MLT could provide better protection.

关键词

低温/褪黑素/缺血再灌注/小鼠/中脑动脉阻塞

Key words

Hypothermia/Melatonin/Ischemia-reperfusion/Mouse/Middle cerebral artery occlusion

引用本文复制引用

陈武,李毅,段发兰,李国玲,陈琴华,张正洪..低温联合褪黑素降低小鼠局灶性脑缺血再灌注损伤[J].湖北医药学院学报,2017,36(1):1-5,封2,6.

基金项目

国家自然科学基金项目(81344438)资助 (81344438)

湖北医药学院学报

2096-708X

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