文章摘要
闫佳佳 伍晓晓 段佳林 文爱东 奚苗苗.楤木皂苷对大鼠心肌缺血/再灌注损伤的保护作用[J].,2015,15(15):2829-2832
楤木皂苷对大鼠心肌缺血/再灌注损伤的保护作用
Protective Effects of Total Saponins Extracted from Aralia Taibaiensis onMyocardial Ischemia/Reperfusion Injury
  
DOI:
中文关键词: 心肌缺血/再灌注损伤  楤木皂苷  抗氧化作用
英文关键词: Myocardial ischemia/reperfusion injury  Total saponins extracted fromAralia taibaiensis  Antioxidant activity
基金项目:国家自然科学基金项目(81470174,81001673)
作者单位
闫佳佳 伍晓晓 段佳林 文爱东 奚苗苗 第四军医大学西京医院药剂科 
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中文摘要:
      目的:观察楤木皂苷(total saponins extracted fromAralia taibaiensis,sAT)对大鼠心肌缺血/再灌注(myocardia1 ischemia/ reperfusion,MI/R)损伤的影响。方法:可逆性冠脉左前降支结扎缺血30 min 再灌注3 h 复制MI/R 模型,将SD 大鼠随机分为假手 术组、模型组、sAT 低、中、高剂量组,每组10 只。采用伊文思蓝(EB)、2,3,5- 氯化三苯基四氮唑蓝(TTC)双染法测定心肌梗死面 积,苏木精- 伊红(HE)染色法观察心肌病理学形态变化,并检测血清中乳酸脱氢酶(LDH)、肌酸激酶同工酶(CK-MB)、超氧化物 歧化酶(SOD)、丙二醛(MDA)、过氧化氢酶(CAT)及谷胱甘肽过氧化物酶(GSH-Px)水平。结果:与模型组比较,sAT 中、高剂量组 可明显缩小心肌梗死面积(P<0.05),并显著降低血清中LDH、CK-MB 及MDA 的含量,同时使得血清中SOD、CAT 和GSH-Px 的 活性增加。且所有给药组心肌组织的病理损伤也小于模型组。结论:sAT 对大鼠MI/R 损伤具有保护作用,其机制可能与抗氧化作 用相关。
英文摘要:
      Objective:To investigate the protective effects of total saponins extracted from Aralia taibaiensis (sAT) on myocardial ischemia/reperfusion injury in rats.Methods:An in vivo model of myocardial ischemia 30 min followed by 3 h reperfusion was made by reversibly ligating coronary left descending artery. The male SD rats were divided randomly into shamgroup; ischemia/reperfusion model group; sAT (60 mg·kg-1; 120 mg·kg-1; 240 mg·kg-1) groups (n=10). The area of myocardial infarction and the change of histological tissue were assessed after 3 h reperfusion. Meanwhile, the levels of lactate dehydrogenase (LDH), creatine kinase-MB (CK-MB), superoxide dismutase (SOD), Malondialdehyde (MDA), catalase (CAT) and glutathione peroxidase (GSH-Px) in serumwere determined by assay kits.Results:Compared with model group, pretreatment with sAT significantly reduced infarct size, decreased the levels of LDH, CK-MB and MDA in the serum, and increased the activities of SOD, CAT and GSH-Px. In addition, sAT improved the pathologic changes of myocardium.Conclusion:sAT has cardioprotective effect against MI/R injury. The mechanism may be related to its antioxidant activities.
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