Marshall P W, Rouse W, Briggs I, Hargreaves R B, Mills S D, McLoughlin B J
ICI Pharmaceuticals, Bioscience Department II, Macclesfield, Cheshire, England.
J Cardiovasc Pharmacol. 1993 Jun;21(6):902-6. doi: 10.1097/00005344-199306000-00008.
We evaluated the cardiovascular effects of the sinoatrial (SA) node modulating agent, ICI D7288, in guinea pig isolated atria and SA node, anaesthetised and exercising dogs, and conscious rats. ICI D7288 (0.1-100 microM) caused a reduction in spontaneous beating rate in guinea pig isolated right atria without affecting the contractile force of paced left atria. The effect was associated with a reduction in the rate of diastolic depolarisation recorded intracellularly from pacemaker cells in the SA node. In anaesthetised dogs, ICI D7288 (0.02-1 mg/kg intravenously, i.v.) caused a dose-related reduction in heart rate (HR) without directly affecting left ventricular (LV) contractility. Exercise tachycardia in dogs was reduced by the compound (0.1-1 mg/kg i.v. and 0.3-10 mg/kg orally, p.o.). The increase in cardiac output (CO) during exercise was well maintained unless the tachycardia was reduced by > 30%, when it was attenuated. Administration of ICI D7288 p.o. (3-100 mg/kg) to conscious rats reduced HR by < or = 40%, but had no effects on blood pressure (BP). We suggest that ICI D7288, through its selective effects on the SA node, may be of use in treatment of ischaemic heart disease to reduce increased HR without impairing cardiac function.
我们评估了窦房(SA)结调节剂ICI D7288对豚鼠离体心房和窦房结、麻醉和运动状态下的犬以及清醒大鼠的心血管效应。ICI D7288(0.1 - 100微摩尔)可使豚鼠离体右心房的自发搏动率降低,而不影响起搏左心房的收缩力。该效应与从窦房结起搏细胞细胞内记录到的舒张期去极化速率降低有关。在麻醉犬中,ICI D7288(静脉注射0.02 - 1毫克/千克)可使心率(HR)呈剂量依赖性降低,而不直接影响左心室(LV)收缩力。该化合物(静脉注射0.1 - 1毫克/千克和口服0.3 - 10毫克/千克)可降低犬的运动性心动过速。运动期间的心输出量(CO)增加可得到良好维持,除非心动过速降低超过30%,此时心输出量会减弱。给清醒大鼠口服ICI D7288(3 - 100毫克/千克)可使心率降低≤40%,但对血压(BP)无影响。我们认为,ICI D7288通过其对窦房结的选择性作用,可能可用于治疗缺血性心脏病,以降低升高的心率而不损害心脏功能。