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新型甾体抗心律失常药物CCI22277对兔心脏的电生理及其他作用

Electrophysiological and other effects on rabbit hearts of CCI22277, a new steroidal antiarrhythmic drug.

作者信息

Campbell T J, Vaughan Williams E M

出版信息

Br J Pharmacol. 1982 Jun;76(2):337-45. doi: 10.1111/j.1476-5381.1982.tb09225.x.

DOI:10.1111/j.1476-5381.1982.tb09225.x
PMID:7093588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2071789/
Abstract

1 CCI22277 (methyl 2 beta-ethoxy-2 alpha-hydroxy-11 alpha-(3-methylbutylamino)-5 alpha-androstane-17 beta-carboxylate hydrochloride) is an aminosteroid with antiarrhythmic properties in animal models. 2 It slowed significantly conduction velocity and spontaneous frequency. 3 CI22277 was a local anaesthetic on frog nerve, 62 times more potent than procaine. It greatly reduced the maximum rate of depolarization (MRD) in atria, Purkinje cells and ventricles, and reduced the overshoot potential. The effects were frequency-dependent and it was concluded that the drug probably delayed recovery from inactivation of fast inward current. 4 CCi2277 had no anti-adrenergic actions, nor did it prolong action potential duration (APD) in any cardiac tissues. 5 The drug was negatively inotropic, and depressed the positive inotropic responses of atria to increased extracellular calcium. 6 At high concentrations and at rapid pacing frequency, the action potential plateau disappeared and APD became very short. 7 It was concluded that CCI is primarily a class I antiarrhythmic drug at low concentration, with additional class IV action at higher concentrations.

摘要
  1. CCI22277(2β - 乙氧基 - 2α - 羟基 - 11α -(3 - 甲基丁基氨基)- 5α - 雄甾烷 - 17β - 羧酸甲酯盐酸盐)是一种在动物模型中具有抗心律失常特性的氨基甾体。2. 它能显著减慢传导速度和自发频率。3. CI22277对蛙神经有局部麻醉作用,效力比普鲁卡因强62倍。它极大地降低了心房、浦肯野细胞和心室的最大去极化速率(MRD),并降低了超射电位。这些作用具有频率依赖性,得出的结论是该药物可能延迟了快速内向电流失活后的恢复。4. CCi2277没有抗肾上腺素能作用,在任何心脏组织中也不延长动作电位时程(APD)。5. 该药物具有负性肌力作用,并抑制心房对细胞外钙增加的正性肌力反应。6. 在高浓度和快速起搏频率下,动作电位平台消失,APD变得非常短。7. 得出的结论是,CCI在低浓度时主要是I类抗心律失常药物,在高浓度时具有额外的IV类作用。

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2
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