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一种新型β-肾上腺素能受体阻断药物ICI 66082对兔乳头肌和犬心脏的作用。

The actions of a new beta-adrenoceptor blocking drug, ICI 66082, on the rabbit papillary muscle and on the dog heart.

作者信息

Harry J D, Knapp M F, Linden R J

出版信息

Br J Pharmacol. 1974 Jun;51(2):169-77. doi: 10.1111/j.1476-5381.1974.tb09644.x.

Abstract

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.

摘要
  1. 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。

  2. 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。

  3. 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。

  4. 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%)。

  5. 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。

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Atrial receptors and heart rate: the efferent pathway.心房感受器与心率:传出通路
J Physiol. 1975 Aug;249(3):581-90. doi: 10.1113/jphysiol.1975.sp011031.

本文引用的文献

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Comparative chronotropic activity of beta-adrenoceptive antagonists.β-肾上腺素能拮抗剂的比较变时活性
Br J Pharmacol. 1970 Nov;40(3):373-81. doi: 10.1111/j.1476-5381.1970.tb10619.x.
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Selective blockade of adrenoceptive beta receptors in the heart.心脏中肾上腺素能β受体的选择性阻断。
Br J Pharmacol Chemother. 1968 Jan;32(1):201-18. doi: 10.1111/j.1476-5381.1968.tb00444.x.
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The pharmacology of beta sympathetic blockade.β-交感神经阻滞的药理学
Am J Cardiol. 1966 Sep;18(3):308-16. doi: 10.1016/0002-9149(66)90047-6.

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