期刊文献+

链脲佐菌素诱导大鼠糖尿病合并心肌缺血再灌注损伤模型的建立与评价 被引量:4

Establishment and Evaluation of Rats Model of Diabetic Myocardial Ischemia-reperfusion Injury Induced by Streptozotocin
下载PDF
导出
摘要 目的建立稳定的大鼠糖尿病合并心肌缺血再灌注损伤模型,为干预实验提供平台。方法 45只健康雄性SD大鼠随机分为正常假手术组(Sham组)、糖尿病模型组(DM组)、糖尿病心肌缺血再灌注损伤模型组(DM+I/R组)。DM组和DM+I/R组一次性腹腔注射链脲佐菌素(STZ)60mg/kg建立糖尿病大鼠模型。DM+I/R组建模成功后采用结扎左冠状动脉前降支30min时进行再灌注120min方法制备缺血再灌注模型,Sham组和DM组仅在左冠状动脉前降支下穿线。于注射STZ后1周、2周、3周、4周观察大鼠空腹血糖、体重、尿量、饮水量及一般情况,用2,3,5-氯化三苯基四氮唑(TTC)测定心肌梗死面积,HE染色,光镜下观察心肌病理学损伤。结果与sham组比较,DM组和DM+I/R组腹腔注射STZ后空腹血糖值显著升高,体重显著下降,尿量和饮水量明显增加(P<0.05);与DM组比较,DM+I/R组心肌梗死面积明显增加(P<0.05),心肌病理学损伤加重。结论本实验方法制备的大鼠糖尿病合并心肌缺血再灌注损伤模型成功率较高,具有较好的稳定性,适用实验研究。 Objective To establish the diabetic myocardial ischemia reperfusion injury model in rats, to provide a platform for inter -vention experiment.Methods Forty five healthy male Sprague Dawley ( SD)rats were randomly divided into three group normalcontrol group ( Sham group) , model of diabetes ( DM group) , diabetes and myocardial ischemia reperfusion injury model group ( DM+I/R group) .Myocardial ischemia was induced by 30 min occlusion of left anterior descending branch of coronary artery followed by 120min reperfusion .The rats of DM group and DM+I/R group by intraperitoneal were injected Streptozotocin ( STZ)( 60 mg/kg)to es -tablish diabetic rats model.After 1 week, 2 weeks, 3 weeks and 4 weeks, the injection of STZ to observe the rats fasting plasma glu -cose, body weight, urine volume, water quantity and the general situation.The myocardial infarction area was measured by tripheny -ltetrazolium chloride TTC.HE staining and myocardial pathology were observed under light damage.Results Compared with thesham group, the fasting blood glucose value in DM group and DM+I/R group were significantly increased after intraperitoneal injec -tion of STZ, the weight was significantly reducted, and the urine volume and water quantity were increased significantly .Comparedwith DM group, the myocardial infarction area of DM+I/R group was obviously increased, myocardial pathology injury aggravated.Conclusion: The experiment method of diabetic myocardial ischemia reperfusion injury in rats model of success rate is higher, hasgood stability, and applied research.
出处 《中西医结合心脑血管病杂志》 2016年第17期1996-1998,共3页 Chinese Journal of Integrative Medicine on Cardio-Cerebrovascular Disease
基金 山西省卫生厅科研基金课题(No.201201045)
关键词 心肌缺血再灌注损伤 糖尿病 链脲佐菌素 myocardial ischemia reperfusion injury diabetes streptozotocin
  • 相关文献

参考文献3

二级参考文献23

  • 1齐云,蔡润兰,刘彬,宋杨,王敏,李永超,赵德明.新药长毒试验动物血液生化测定规范化研究系列之五——SPF级SD大鼠血液生化参考值的建立[J].中国比较医学杂志,2006,16(4):193-196. 被引量:36
  • 2Ong SB, Hausenloy DJ. Mitochondrial morphology and cardiovascular disease[J]. Cardiovasc Res,2010,88(1) : 16-29.
  • 3Bclenguer P, Pellegrini L. The dynamin GTPasc OPAl: more than mitoehondrla[ J] ? Biochim Biophys Aeta, 2013,1833( 1 ) : 176-183.
  • 4Ong SB, Subrayan S, Lira SY, ct al. Inhibiting mitochondrial fission protects the heart against ischemia/reperfusion injury [ J ]. Circulation, 2010,121 ( 18), 2012-2022.
  • 5Calo L, Dong Y, Kumar R, et al. Mitochondrial dynamics: an eme- rging paradigm in ischemia-reperfusion injury[ J]. Curr Pharm Des, 2013,19(39) :6848-6857.
  • 6刘悦,刘玉华,黄立宁,等.七氟醚后处理对大鼠心肌缺血再灌注时细胞凋亡的影响[J].中华麻醉学杂志,2011,31(12):1477-1480.
  • 7Ishihara N, Otera H, Oka T, et al. Regulation and physiologic fun- ctions of GTPases in mitochondrial fusion and fission in mammals[J]. Antioxid Redox Signal, 2013,19 (4) : 389-399.
  • 8Hwang SJ, Kim W. Mitochondrial dynamics in the heart as a novel therapeutic target for cardioprotection[ J ]. Chonnam Med J, 2013,49 (3) :101-107.
  • 9Disatnik MH, Ferreira JC, Campos JC, et al. Acute inhibition of excessive mitochondrial fission after myocardial infarction prevents long-term cardiac dysfunction [ J ]. J Am Heart Assoc, 2013,2 (5) : e000461.
  • 10Cheu L, Gong Q, Stice JP, et al. Mitochondrial OPAl,apoptosis, and heart failure[ J]. Cardiovasc Res, 2009,84 ( 1 ) : 91-99.

共引文献16

同被引文献13

引证文献4

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部