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ICI 50172与(-)-普萘洛尔的抗心律失常作用比较及其对细胞内心脏动作电位和心脏功能其他特征的影响。

A comparison of the anti-arrhythmic actions of I.C.I. 50172 and (--)-propranolol and their effects on intracellular cardiac action potentials and other features of cardiac function.

作者信息

Papp J G, Williams E M

出版信息

Br J Pharmacol. 1969 Oct;37(2):391-9. doi: 10.1111/j.1476-5381.1969.tb10576.x.

Abstract
  1. I.C.I. 50172 had marked quinidine-like effects on intracellular cardiac action potentials at concentrations above 20 mg/l. (6.61 x 10(-5)M). The rate of rise and overshoot of the action potential, conduction velocity and contractions were decreased. (-)-Propranolol had similar effects at less than 1/30 this concentration.2. I.C.I. 50172 had 1/100 the activity of (-)-propranolol as a local anaesthetic. Since this is also the ratio of their in vitro beta-receptor blocking activities, I.C.I. 50172 provides no net increase in specificity of beta-receptor blockade.3. In contrast, the in vivo activity of I.C.I. 50172 in protecting anaesthetized guinea-pigs against ouabain-induced ventricular fibrillation was 40% that of (-)-propranolol.4. Structure-activity relations of beta-receptor blocking drugs are discussed.
摘要
  1. I.C.I. 50172在浓度高于20毫克/升(6.61×10⁻⁵摩尔/升)时,对细胞内心脏动作电位具有明显的奎尼丁样效应。动作电位的上升速率和超射、传导速度及收缩均降低。(-)-普萘洛尔在该浓度的不到1/30时具有类似效应。

  2. I.C.I. 50172作为局部麻醉剂的活性是(-)-普萘洛尔的1/100。由于这也是它们体外β受体阻断活性的比例,所以I.C.I. 50172并未使β受体阻断的特异性净增加。

  3. 相比之下,I.C.I. 50172在保护麻醉豚鼠免受哇巴因诱导的心室颤动方面的体内活性是(-)-普萘洛尔的40%。

  4. 讨论了β受体阻断药物的构效关系。

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本文引用的文献

1
Antifibrillatory action.抗纤颤作用。
J Physiol. 1962 Mar;160(3):470-82. doi: 10.1113/jphysiol.1962.sp006860.
5
A NEW ADRENERGIC BETARECEPTOR ANTAGONIST.一种新型肾上腺素能β受体拮抗剂。
Lancet. 1964 May 16;1(7342):1080-1. doi: 10.1016/s0140-6736(64)91275-9.
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A comparison of tests for antifibrillatory action.抗纤颤作用测试的比较
Br J Pharmacol Chemother. 1961 Dec;17(3):424-32. doi: 10.1111/j.1476-5381.1961.tb01129.x.

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