Comparative pharmacology of calcium antagonists: nifedipine, verapamil and diltiazem.

Abstract

Calcium antagonists (slow channel blocking agents) are a very heterogeneous group of agents with dissimilar structural, electrophysiologic and pharmacologic properties. Nifedipine is a potent, long-acting vasodilator that has proved highly efficacious in relieving anginal symptoms caused by coronary vasospasm. In vivo, it exerts no myocardial depressant effects and has no antiarrhythmic properties. Treatment with nifedipine can safely be combined with administration of a beta receptor blocking agent. VErapamil prolongs atrioventricular (A-V) conduction (A-H interval) in a dose-dependent manner. It is the drug of choice for the treatment of reentrant supraventricular arrhythmias, irrespective of whether reentry occurs within the A-V node or through an accessory pathway (the Wolff-Parkinson-White syndrome). Verapamil is only moderately effective as an antianginal agent. Diltiazem is efficacious for the treatment of angiospastic angina, but its value as an antiarrhythmic agent remains to be delineated.

• Authors: P D Henry
• Journal: The American journal of cardiology (Am J Cardiol) Vol. 46 Issue 6 Pg. 1047-58 (Dec 01 1980) ISSN: 0002-9149 [Print] United States
• PMID: 6255787 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S., Review)

Chemical References

• Benzazepines
• Ion Channels
• Pyridines
• Vasodilator Agents
• Tetrodotoxin
• Verapamil
• Diltiazem
• Nifedipine
• Calcium

Topics

• Angina Pectoris (drug therapy)
• Angina Pectoris, Variant (drug therapy)
• Animals
• Arrhythmias, Cardiac (drug therapy)
• Benzazepines (pharmacology)
• Calcium (antagonists & inhibitors)
• Cardiovascular System (drug effects)
• Diltiazem (metabolism, pharmacology, therapeutic use)
• Dogs
• Electrophysiology
• Humans
• Hypertension (drug therapy)
• Ion Channels (drug effects)
• Kinetics
• Muscle, Smooth, Vascular (drug effects)
• Myocardial Contraction (drug effects)
• Myocardial Infarction (drug therapy)
• Nifedipine (metabolism, pharmacology, therapeutic use)
• Pyridines (pharmacology)
• Sheep
• Tetrodotoxin (pharmacology)
• Vasodilator Agents
• Verapamil (metabolism, pharmacology, therapeutic use)