Suppr超能文献

[延迟电去耦联参与κ-阿片受体激活诱导的离体大鼠心脏心脏保护作用]

[Delayed electrical uncoupling is involved in kappa-opioid receptor activation -induced cardioprotective effect in the isolated rat heart].

作者信息

Chen Bao-Ping, Fan Fang-Yan, Mao Hong-Jiao, Xia Qiang

机构信息

Department of Physiology, Shaoxing University School of Medicine, Shaoxing 312000, China.

出版信息

Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2006 Feb;22(1):64-70.

Abstract

AIM

To determine whether activation of kappa-opioid receptor with U50,488H, a selective kappa-opioid receptor agonist, produces any changes in electrical uncoupling during prolonged ischemia and whether these changes in electrical uncoupling is associated with the cardioprotection induced by kappa-opioid receptor activation, and to explore the possible mechanism.

METHODS

(1) To observe the effect of U50,488H (10(-7), 10(-6), 3 x10(-6) and 10(-5) mol/L), a selective kappa-opioid receptor agonist, or with a selective kappa-opioid receptor antagonist nor-BNI (5 x 10(-6) mol/L), or with a mitochondrial K(ATP) channel inhibitor 5-HD on myocardium during ischemia/reperfusion in isolated perfused rat heart. Parameters of measurements include hemodynamic data, formazan content, heart rate, coronary flow, and lactate dehydrogenase (LDH). (2) To examine the effect of U50,488H of different concentration on electrical coupling parameters (including onset of uncoupling, plateau time, slope, and fold increase in r1) during 70 min myocardial ischemia in isolated perfused rat heart.

RESULTS

(1) Pretreatment with U50,488H concentration dependently increased formazan content and reduced LDH release induced by 30 min of ischemia and 120 min of reperfusion. (2) The onset of electrical uncoupling and plateau time during prolonged ischemia was delayed by kappa-opioid receptor activation with U50,488H. (3) Linear regression analysis shown that the increase in formazan content and decrease in LDH release produced by kappa-opioid receptor activation was associated with delayed electrical uncoupling during prolonged ischemia. (4) The effects of U50,488H on formazan content, LDH release and on electrical coupling were abolished by nor-BNI, or 5-HD.

CONCLUSION

This results demonstrate that the onset of electrical uncoupling during prolonged ischemia is delayed by kappa-opioid receptor activation with a selective kappa-opioid receptor agonist U50,488H, and that delayed electrical uncoupling is associated with the cardioprotection induced by kappa-opioid receptor activation with U50,488H. These effects of kappa-opioid receptor activation with U50,488H are mediated by mitochondrial K(ATP) channels.

摘要

目的

确定使用选择性κ-阿片受体激动剂U50,488H激活κ-阿片受体是否会在长时间缺血期间引起电脱耦联的任何变化,以及电脱耦联的这些变化是否与κ-阿片受体激活诱导的心脏保护作用相关,并探讨其可能的机制。

方法

(1)观察选择性κ-阿片受体激动剂U50,488H(10⁻⁷、10⁻⁶、3×10⁻⁶和10⁻⁵mol/L),或与选择性κ-阿片受体拮抗剂nor-BNI(5×10⁻⁶mol/L),或与线粒体K⁺-ATP通道抑制剂5-HD对离体灌注大鼠心脏缺血/再灌注期间心肌的影响。测量参数包括血流动力学数据、甲臜含量、心率、冠脉流量和乳酸脱氢酶(LDH)。(2)研究不同浓度的U50,488H对离体灌注大鼠心脏70分钟心肌缺血期间电耦联参数(包括脱耦联起始时间、平台期时间、斜率和r1增加倍数)的影响。

结果

(1)U50,488H预处理呈浓度依赖性增加甲臜含量,并减少30分钟缺血和120分钟再灌注诱导的LDH释放。(2)U50,488H激活κ-阿片受体可延迟长时间缺血期间电脱耦联的起始时间和平台期时间。(3)线性回归分析表明,κ-阿片受体激活引起的甲臜含量增加和LDH释放减少与长时间缺血期间电脱耦联延迟有关。(4)nor-BNI或5-HD可消除U50,488H对甲臜含量、LDH释放和电耦联的影响。

结论

这些结果表明,使用选择性κ-阿片受体激动剂U50,488H激活κ-阿片受体可延迟长时间缺血期间电脱耦联的起始时间,且电脱耦联延迟与U50,488H激活κ-阿片受体诱导的心脏保护作用相关。U50,488H激活κ-阿片受体的这些作用是由线粒体K⁺-ATP通道介导的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验