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用于测试药物致心律失常作用的体外和体内模型。

In vitro and in vivo models for testing arrhythmogenesis in drugs.

作者信息

Carlsson L

机构信息

AstraZeneca R&D Mölndal, Integrative Pharmacology, Mölndal, Sweden.

出版信息

J Intern Med. 2006 Jan;259(1):70-80. doi: 10.1111/j.1365-2796.2005.01590.x.

Abstract

The steadily increasing list of drugs associated with prolongation of the QT interval and torsades de pointes (TdP) constitute a medical problem of major concern. Hence, there is a need at an early stage to identify drug candidates with an inherent capacity to induce repolarization-related proarrhythmias, avoiding exposure of large populations to potentially harmful drugs. Furthermore, the availability of clinically relevant and predictive animal models should reduce the risk that effective and potentially life-saving drugs never reach the market. This review will discuss the pros and cons of some in vivo and in vitro animal models for assessing proarrhythmia liability.

摘要

与QT间期延长和尖端扭转型室速(TdP)相关的药物清单不断增加,这构成了一个备受关注的医学问题。因此,有必要在早期阶段识别具有诱发复极相关心律失常内在能力的候选药物,避免大量人群接触潜在有害药物。此外,具备临床相关性和预测性的动物模型应能降低有效且可能挽救生命的药物无法上市的风险。本综述将讨论一些用于评估心律失常风险的体内和体外动物模型的优缺点。

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