How Ca1.2-bound verapamil blocks Ca influx into cardiomyocyte: Atomic level views.

The first clinically used antiarrhythmic, antianginal and anti-hypertensive phenylalkylamine, verapamil's cardiovascular activity is inextricably linked to its ability to antagonize Ca overload via blocking Ca1.2, a cardiac L-type Ca channel of undisputed physiological and pharmacological importance in cardiovascular disorders such as myocardial ischemia-reperfusion injury. From a structural point of view, however, the action mechanism of verapamil is still elusive. Therefore, incorporating previous findings for verapamil and Ca1.2, this review article puts forward two experimental data-derived and -supported 3D structure models for Ca1.2's α subunit and its verapamil-bound form. Furthermore, this article suggests three biophysical mechanisms, namely competitive binding, steric hindrance and electrostatic repulsion, towards an atomic level understanding of how verapamil blocks the L-type Ca current mediated by Ca1.2 in reality, which can be useful for the design and development of next-generation Ca antagonists to provide safer and more effective treatment of cardiovascular diseases.

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