Ono H, Himori N, Taira N
Tohoku J Exp Med. 1977 Apr;121(4):383-90. doi: 10.1620/tjem.121.383.
Chronotropic effects of 6 coronary vasodilators, carbochromen, dilazep, diltiazem, dipyridamole, nifedipine and verapamil, were compared by close-arterial administration to the isolated, blood-perfused sino-atrial node preparation of the dog. All drugs produced a dose-related decrease in sinus rate, and the order of negative chronotropic potency determined on a weight basis was as follows: (formula: see text). Higher doses of these drugs except dipyridamole caused atrial standstill. The order of potency causing atrial standstill determined on a weight basis was as follows: (formula: see text). Dipyridamole in lower doses produced a negative chronotropic effect alone, but with higher doses a positive chronotropic effect preceded a negative one. Carbochromen in a wide range of doses produced a triphasic response consisting of initial brief positive, succeeding main negative and final gradually-developing slight positive components.
通过向犬的离体、血液灌注的窦房结标本进行动脉内给药,比较了6种冠状血管扩张剂(卡波孟、地拉卓、地尔硫䓬、双嘧达莫、硝苯地平和维拉帕米)的变时作用。所有药物均使窦性心率呈剂量依赖性降低,以重量为基础测定的负性变时效力顺序如下:(公式:见原文)。除双嘧达莫外,这些药物的较高剂量均导致心房停搏。以重量为基础测定的导致心房停搏的效力顺序如下:(公式:见原文)。较低剂量的双嘧达莫单独产生负性变时作用,但较高剂量时,正性变时作用先于负性变时作用出现。卡波孟在很宽的剂量范围内产生三相反应,包括最初短暂的正性、随后主要的负性和最终逐渐出现的轻微正性成分。