Noguchi K, Ojiri Y, Nagamine F, Matsuzaki T, Sakanashi M
Department of Pharmacology, School of Medicine, Faculty of Medicine, University of the Ryukyus, Okinawa, Japan.
Eur J Pharmacol. 1989 Sep 22;168(3):315-28. doi: 10.1016/0014-2999(89)90793-0.
Hemodynamic parameters, segment shortening in the ischemic myocardium and cardiac lactate extraction were estimated in the presence of a critical coronary stenosis, before and after administration of the selective beta 2-adrenoceptor antagonist, ICI 118,551, or the beta 1-adrenoceptor antagonist, atenolol, to anesthetized dogs. ICI 118,551 (0.2 and 0.5 mg/kg i.v.) and atenolol (0.2 mg/kg i.v.) produced significant decreases in both heart rate (by 6, 14 and 20% of the predrug value, respectively) and maxLVdP/dt (by 15, 26 and 24% of the predrug value, respectively). ICI 118,551 (0.5 mg/kg) and atenolol significantly improved the impaired shortening of the myocardial segment when compared with the change seen after saline administration. ICI 118,551 at both doses and atenolol significantly increased depressed cardiac lactate extraction while saline did not. Increasing heart rate by pacing abolished the beneficial effects of ICI 118,551 and atenolol on ischemic myocardial segment shortening and lactate metabolism. The data suggest that not only beta 1- but also beta 2-adrenoceptor blockade may contribute to the amelioration of myocardial ischemia in a model of coronary stenosis.
在麻醉犬的冠状动脉严重狭窄情况下,分别在给予选择性β2 -肾上腺素能受体拮抗剂ICI 118,551或β1 -肾上腺素能受体拮抗剂阿替洛尔之前和之后,评估血流动力学参数、缺血心肌节段缩短情况以及心脏乳酸摄取。静脉注射ICI 118,551(0.2和0.5毫克/千克)和阿替洛尔(0.2毫克/千克)均使心率(分别降低至给药前值的6%、14%和20%)和左心室最大dp/dt(分别降低至给药前值的15%、26%和24%)显著下降。与给予生理盐水后的变化相比,ICI 118,551(0.5毫克/千克)和阿替洛尔显著改善了心肌节段缩短受损的情况。两种剂量的ICI 118,551和阿替洛尔均显著增加了降低的心脏乳酸摄取,而生理盐水则无此作用。通过起搏增加心率消除了ICI 118,551和阿替洛尔对缺血心肌节段缩短和乳酸代谢的有益作用。数据表明,在冠状动脉狭窄模型中,不仅β1 -而且β2 -肾上腺素能受体阻断可能有助于改善心肌缺血。