Lishmanov A Iu, Lasukova T V, Maslov L N, Platonov A A
Ross Fiziol Zh Im I M Sechenova. 2006 Dec;92(12):1419-28.
It was found that pretreatment of rats with selective agonist of kappa1-opioid receptors (OR) (-)--U--50.488 decreased the incidence of ischemic (10 min) and reperfusion (10 min) ventricular arrhythmias. The selective kappa2-OR agonist GR-89696 had no effect on the incidence of ventricular arrhythmias during a 10-min coronary artery occlusion and following reperfusion in anesthetized rats. The effect of (-)--U-50.488 was abolished by the selective kappa1-OR antagonist of non-binaltorphimine and the non-selective peripheral OR antagonist naloxone methiodide. Perfusion of isolated rat heart with (-)--U-50.488 did not affect arrhythmias during ischemia and reperfusion. The authors suggest that stimulation of kappa1-opioid receptors located outside the central nervous system increases heart resistance against arrhythmogenic action of ischemia/reperfusion, antiarrhythmic action of (-)--U-50.488 being mediated through extracardiac opioid receptors.
研究发现,用κ1-阿片受体(OR)的选择性激动剂(-)- - U - 50,488对大鼠进行预处理,可降低缺血(10分钟)和再灌注(10分钟)时室性心律失常的发生率。选择性κ2-OR激动剂GR - 89696对麻醉大鼠冠状动脉闭塞10分钟期间及再灌注后的室性心律失常发生率没有影响。非双纳曲酮的选择性κ1-OR拮抗剂和非选择性外周OR拮抗剂甲硫氨酸纳洛酮可消除(-)- - U - 50,488的作用。用(-)- - U - 50,488灌注离体大鼠心脏,对缺血和再灌注期间的心律失常没有影响。作者认为,刺激位于中枢神经系统之外的κ1-阿片受体可增加心脏对缺血/再灌注致心律失常作用的抵抗力,(-)- - U - 50,488的抗心律失常作用是通过心外阿片受体介导的。