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作 者:杨运海[1] 韩召敏[1] 李伟栋[1] 屠政良[1] 倪一鸣[1]
机构地区:[1]浙江大学医学院附属第一医院心胸外科,杭州310003
出 处:《中华急诊医学杂志》2009年第3期274-276,共3页Chinese Journal of Emergency Medicine
基 金:基金项目:教育部留学回国人员科研启动基金[教外司留(2001)345]
摘 要:目的观察三硝基丙酸(3-NPA)预处理对缺血-再灌注兔心肌细胞凋亡的影响及其机制。方法24只新西兰大耳兔随机分为对照组(C组)、实验组(3-NPA组)和阻滞剂组(5-HD组),每组8只。5-HD组在开胸前24h通过耳缘静脉注射特异性线粒体ATP敏感钾通道阻滞剂5-羟基癸酸(5mg·k^-1),C组和3-NPA组注射同样体积的生理盐水。10min后3-NPA组和5-HD组注射3-硝基丙酸(3mg·kg^-1),C组注射同样体积的生理盐水。通过结扎兔左冠状动脉建立心肌缺血-再灌注动物模型,三组缺血30min再灌注120min。检测再灌注120min后心肌梗死面积、心肌细胞凋亡指数、Bcl-2和Bax蛋白的表达。对实验数据进行方差分析检验。结果3-NPA组的心肌梗死面积显著低于其它C组[(0.26±0.07)vs.(0.45±0.09),P〈0.01]和5-HD组[(0.26±0.07)vs.(0.40±0.07),P〈0.01];C组和5-HD组之间没有显著性差异[(0.45±0.09)vs.(0.40±0.07),P〉0.05]。3-NPA组心肌细胞凋亡指数明显小于C组[(27.72±5.18)vs.(45.91±10.54),P〈0.01]和5-HD组[(27.72±5.18)vs.(43.44±7.33),P〈0.01]。3-NPA组bcl-2表达高于另外两组[(0.123±0.046)vs.(0.079±0.019),(0.080±0.019),P〈0.05],而Bax明显低于另外两组[(0.095±0.020)vs.(0.14±0.05)and(0.15±0.05),P〈0.05]。结论3-NPA预处理对缺血-再灌注心肌具有良好的抗凋亡作用,这与其开放断线粒体ATP敏感钾通道有关。Objective To investigate the effects of preconditioning with 3-nitropropionic acid on myocardial apoptosis induced by ischemia-reperfusion injury. Method Twenty-four rabbits were randomly divided into control group (group C, n = 8), precondition group (group 3-NPA, n = 8) and 5-HD group (group 5-HD, n = 8). The group 5-HD was treated intravenously with 5 mg·kg^-1 5-HD (ATP-sensitive potassium channels blocker), group C and group 3-NPA received normal saline instead of 5-HD. Ten minutes later, 5-HD group and 3-NPA group were injected with 3-NPA (3 mg·kg^-1) and the group C was injected with normal saline. Twenty-four hours later, the left anterior descending coronary artery was ligated for 30 min and then unclamped for 120 min to establish ischemia-reperfnsion injury model. After reperfusion, the infarct sizes of ventricular myocardium, apoptotic myocardial cells and the expressions of Bcl-2 and Bax protein were measured. Results Infarct sizes and apoptotic myocardial cells in group 3-NPA were less than those in the others ( P 〈 0.01). The expressions of Bcl-2 in group 3-NPA increased as compared with group C (P 〈 0.05) and group 5-HD (P 〈 0.05), whereas the expressions of Bax in group 3-NPA decreased as compared with group C ( P 〈 0.05) and group 5-HD ( P 〈 0.05). Conclusions Preconditioning with 3-nitropropionic acid reduces myocardial apoptosis induced by ischemia-reperfusion injury which is attributed to the opening of mitochondrial KATP channels.
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