Harry J D, Knapp M F, Linden R J
Br J Pharmacol. 1974 Jun;51(2):169-77. doi: 10.1111/j.1476-5381.1974.tb09644.x.
1 The actions of 4-(2-hydroxy-3-isopropylaminopropoxy) phenyl acetamide (ICI 66082), a new beta-adrenoceptor blocking drug, on the twitch response of the isolated papillary muscle of the rabbit and on dP/dt max and free heart rate of a denervated dog heart preparation, are described.2 ICI 66082 (up to 1 mg/ml) did not produce any depression of the twitch response of the rabbit papillary muscle. ICI 66082 antagonized the action of isoprenaline on this preparation at a concentration of 0.01 mug/ml.3 ICI 66082 (0.5-1.0 mg/kg intravenously) reduced the control value of dP/dt max in four dog preparations by a mean value of 529 mmHg/s (s.e. mean +/- 139 mm Hg/s), with no significant change in free heart rate. Antagonism of the effect of isoprenaline on dP/dt max and on free heart rate was demonstrated with ICI 66082 (0.1 mg/kg).4 ICI 66082 (1.0-1.5 mg/kg) produced no significant changes in dP/dt max or in free heart rate in four dogs pretreated with reserpine. A significant reduction (16% of the control value) in dP/dt max was observed with ICI 66082 at a high dose of 40-50 mg/kg.5 It is concluded that ICI 66082 is a competitive antagonist against the actions of isoprenaline on cardiac muscle, has no negative inotropic action (unless the dose exceeds 40 mg/kg) and lacks intrinsic sympathomimetic activity.
描述了一种新型β-肾上腺素受体阻断药物4-(2-羟基-3-异丙氨基丙氧基)苯乙酰胺(ICI 66082)对兔离体乳头肌抽搐反应以及对去神经犬心脏标本的最大dp/dt和自由心率的作用。
ICI 66082(浓度高达1mg/ml)未对兔乳头肌的抽搐反应产生任何抑制作用。ICI 66082在浓度为0.01μg/ml时可拮抗异丙肾上腺素对该标本的作用。
ICI 66082(静脉注射0.5 - 1.0mg/kg)使四只犬标本的最大dp/dt对照值平均降低529mmHg/s(标准误±139mmHg/s),自由心率无显著变化。ICI 66082(0.1mg/kg)可拮抗异丙肾上腺素对最大dp/dt和自由心率的作用。
ICI 66082(1.0 - 1.5mg/kg)对四只预先用利血平处理的犬的最大dp/dt或自由心率未产生显著变化。在高剂量40 - 50mg/kg时,ICI 66082使最大dp/dt显著降低(为对照值的16%)。
得出结论:ICI 66082是异丙肾上腺素对心肌作用的竞争性拮抗剂,无负性肌力作用(除非剂量超过40mg/kg)且缺乏内在拟交感活性。