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LY175326的药理学:一种具有血管舒张活性的强效强心剂。

Pharmacology of LY175326: a potent cardiotonic agent with vasodilator activities.

作者信息

Hayes J S, Pollock G D, Wilson H, Bowling N, Robertson D W

出版信息

J Pharmacol Exp Ther. 1985 May;233(2):318-26.

PMID:3999023
Abstract

Compound LY175326 is one of a series of novel cardiovascular agents with both inotropic and vasodilator activities. In cat papillary muscles, LY175326 increased contractility in a concentration-dependent manner; these actions were not blocked by prazosin, propranolol or cimetidine. Inotropic responses were observed in unpaced, perfused guinea-pig hearts and these effects were associated with modest increases in heart rate and coronary flow. An i.v. dose of 0.1 mg/kg of LY175326 caused 54 and 95% increases in contractility in either the anesthetized cat or dog, respectively; corresponding heart rates were increased by less than 10%. Oral administration of 0.5 mg/kg to dogs was associated with an inotropic response that was maximal between 60 and 90 min and lasted in excess of 3 hr. These effects were not accompanied by increases in heart rate, gross behavioral changes or emesis. The pharmacology of LY175326 was evaluated in a propranolol-induced heart failure model using anesthetized beagle dogs. A bolus injection of 0.15 mg/kg of LY175326 followed by an infusion of 0.4 mg/kg/hr reversed the hemodynamic symptoms of heart failure by increasing left ventricular dP/dt60, cardiac output and stroke volume and reducing left atrial filling pressure and vascular resistance; heart rate was unchanged and calculated myocardial oxygen consumption was reduced. This balance of inotropic:vasodilator activities may provide a means of improving cardiac function while maintaining the myocardial oxygen supply:demand.

摘要

化合物LY175326是一系列具有正性肌力和血管舒张活性的新型心血管药物之一。在猫乳头肌中,LY175326以浓度依赖性方式增加收缩力;这些作用不受哌唑嗪、普萘洛尔或西咪替丁的阻断。在未起搏的灌注豚鼠心脏中观察到正性肌力反应,这些作用与心率和冠状动脉血流量的适度增加有关。静脉注射0.1mg/kg的LY175326分别使麻醉猫或狗的收缩力增加54%和95%;相应的心率增加不到10%。给狗口服0.5mg/kg与正性肌力反应有关,该反应在60至90分钟之间达到最大值,并持续超过3小时。这些作用不伴有心率增加、明显的行为变化或呕吐。使用麻醉的比格犬在普萘洛尔诱导的心力衰竭模型中评估了LY175326的药理学。静脉推注0.15mg/kg的LY175326,随后以0.4mg/kg/小时的速度输注,通过增加左心室dP/dt60、心输出量和每搏输出量以及降低左心房充盈压和血管阻力,逆转了心力衰竭的血流动力学症状;心率不变,计算得出的心肌耗氧量降低。这种正性肌力与血管舒张活性的平衡可能提供一种在维持心肌氧供应与需求的同时改善心脏功能的方法。

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