Target Localization and Electrophysiology
The primary sites of action for beta-blockers are β₁-receptors, located in the cardiac pacemaker cells and working ventricular cardiomyocytes.
Blockade of these receptors induces several electrophysiological effects in the heart:
- Decreased automaticity.
- Suppressed conduction velocity.
- Decreased excitability.
- Prolongation of the effective refractory period (ERP) throughout all myocardial regions.
Classification and Clinical Spectrum
In clinical practice, these drugs are divided into two main categories:
- Cardioselective (selectively acting on β₁-receptors): metoprolol, atenolol, talinolol.
- Non-selective (blocking both β₁- and β₂-receptors): propranolol.
Due to their electrophysiological properties, these medications demonstrate high efficacy in treating both types of tachyarrhythmias — supraventricular and ventricular.
Adverse Effects
Therapy with beta-blockers may lead to adverse reactions. Common side effects for the entire class relate to the suppression of cardiac activity:
- Bradycardia.
- Conduction disturbances, such as atrioventricular block.
- Decreased myocardial contractility (negative inotropic effect).
Non-selective agents like propranolol are associated with specific complications due to extra-cardiac blockade of β₂-receptors: bronchospasm and peripheral vasospasm.