Dage R C, Roebel L E, Hsieh C P, Weiner D L, Woodward J K
J Cardiovasc Pharmacol. 1982 May-Jun;4(3):500-8.
The cardiovascular properties of a new noncatechol, nonglycoside cardiotonic agent, MDL 17,043, were investigated in anesthetized and conscious dogs and the dog heart-lung preparation. MDL 17,043 (0.1-1 mg/kg), administered to anesthetized dogs by intravenous injection, produced dose-related increases in cardiac contractile force lasting more than 1 h. It also produced relatively minor and shorter-lasting increases in heart rate, and brief decreases in blood pressure. These effects were not blocked by propranolol. Of these effects, the increase in cardiac contractile force was, by far, the most prominent. the cardiac effects were also observed in the dog heart-lung preparation. When administered to anesthetized dogs by constant intravenous infusion, MDL 17,043 (09.03 and 0.1 mg/kg/min) produced a marked and sustained increase in cardiac contractile force and a sustained decrease in blood pressure without altering heart rate, suggesting a wide separation between the inotropic instrumented dogs, MDL 17,043 (3-30 mg/kg) produced a sustained increase in dP/dt without altering heart rate or blood pressure. It reversed the depressant effect of pentobarbital on the ventricular function curve in the dog heart-lung. When the hemodynamic characteristics of compensated heart failure were produced by propranolol in anesthetized dogs, MDL 17,043 reversed these effects. These studies suggest that MDL 17,043 may have a beneficial effect in the treatment of heart failure.
在麻醉和清醒犬以及犬心肺制备模型中,对一种新型非儿茶酚、非糖苷类强心剂MDL 17,043的心血管特性进行了研究。静脉注射给予麻醉犬MDL 17,043(0.1 - 1毫克/千克),可使心脏收缩力呈剂量依赖性增加,持续超过1小时。它还使心率产生相对较小且持续时间较短的增加,并使血压短暂下降。这些作用未被普萘洛尔阻断。在这些作用中,心脏收缩力的增加最为显著。在犬心肺制备模型中也观察到了心脏效应。当通过持续静脉输注给予麻醉犬MDL 17,043(0.03和0.1毫克/千克/分钟)时,可使心脏收缩力显著且持续增加,血压持续下降,而心率不变,这表明变力作用与其他作用之间有很大区别。在有创监测的犬中,MDL 17,043(3 - 30毫克/千克)可使dP/dt持续增加,而不改变心率或血压。它逆转了戊巴比妥对犬心肺心室功能曲线的抑制作用。当普萘洛尔在麻醉犬中产生代偿性心力衰竭的血流动力学特征时,MDL 17,043可逆转这些作用。这些研究表明,MDL 17,043可能对心力衰竭的治疗有有益作用。