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大麻素受体在缺血/再灌注期间心脏收缩性调节中的作用。

Role of cannabinoid receptors in the regulation of cardiac contractility during ischemia/reperfusion.

作者信息

Maslov L N, Lasukova O V, Krylatov A V, Hanus L O, Pertwee R, Ivanchuk I I, Crowford D

机构信息

Institute of Cardiology, Siberian Division of the Russian Academy of Medical Sciences, Tomsk.

出版信息

Bull Exp Biol Med. 2006 Nov;142(5):557-61. doi: 10.1007/s10517-006-0417-4.

Abstract

We studied the effect of selective ligands of cannabinoid (CB) receptors on contractility of isolated Langendorff-perfused rat heart under conditions of 45-min total ischemia and 30-min reperfusion. Perfusion with a solution containing selective CB receptor agonist HU-210 for 10 min before ischemia increased the severity of reperfusion contractile dysfunction. This drug decreased left ventricular developed pressure and maximum rates of contraction and relaxation, but had no effect on heart rate and end-diastolic pressure. The negative inotropic effect of the drug was transitory and disappeared after 5-min reperfusion. Pretreatment with selective CB1 receptor antagonist SR141716A and selective CB2 receptor antagonist SR144528 had no effect on heart rate and myocardial contractility during reperfusion. Our results indicate that stimulation of CB receptors can increase the degree of reperfusion-induced cardiac contractile dysfunction. However, endogenous cannabinoids are not involved in the development of myocardial contractile dysfunction during ischemia/reperfusion of the isolated heart.

摘要

我们研究了大麻素(CB)受体选择性配体对离体Langendorff灌注大鼠心脏在45分钟全心缺血和30分钟再灌注条件下收缩性的影响。在缺血前用含选择性CB受体激动剂HU - 210的溶液灌注10分钟会增加再灌注收缩功能障碍的严重程度。该药物降低了左心室发展压以及收缩和舒张的最大速率,但对心率和舒张末期压力没有影响。该药物的负性肌力作用是短暂的,在再灌注5分钟后消失。选择性CB1受体拮抗剂SR141716A和选择性CB2受体拮抗剂SR144528预处理对再灌注期间的心率和心肌收缩性没有影响。我们的结果表明,刺激CB受体会增加再灌注诱导的心脏收缩功能障碍的程度。然而,内源性大麻素不参与离体心脏缺血/再灌注期间心肌收缩功能障碍的发生。

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