Calcium Antagonists

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During electrical excitation of the cell membrane of heart or smooth muscle, different ionic currents are activated, including an inward Ca2+ current. The term Ca2+ antagonist is applied to drugs that inhibit the influx of Ca2+ ions without affecting inward Na+ or outward K+ currents to a significant degree. Other labels are Ca-entry blocker or Ca-channel blocker. Therapeutically used Ca2+ antagonists can be divided into three groups according to their effects on heart and vasculature.

I. Dihydropyridine derivatives. The dihydropyridines, e.g., nifedipine, are uncharged hydrophobic substances. They induce a relaxation of vascular smooth muscle in arterial beds. An effect on cardiac function is practically absent at therapeutic dosage. (However, in pharmacological experiments on isolated cardiac muscle preparations a clear negative inotropic effect is demonstrable.) They are thus regarded as va-soselective Ca2+ antagonists. Because of the dilatation of resistance vessels, blood pressure falls. Cardiac afterload is diminished (p. 306) and, therefore, also oxygen demand. Spasms of coronary arteries are prevented.

Indications for nifedipine include angina pectoris (p. 308) and, — when applied as a sustained release preparation, — hypertension (p. 312). In angina pectoris, it is effective when given either prophylactically or during acute attacks. Adverse effects are palpitation (reflex tachycardia due to hypotension), headache, and pretibial edema.

Nitrendipine and felodipine are used in the treatment of hypertension. Ni-modipine is given prophylactically after subarachnoidal hemorrhage to prevent vasospasms due to depolarization by excess K+ liberated from disintegrating erythrocytes or blockade of NO by free hemoglobin.

II. Verapamil and other catamphi-philic Ca2+ antagonists. Verapamil contains a nitrogen atom bearing a positive charge at physiological pH and thus rep resents a cationic amphiphilic molecule. It exerts inhibitory effects not only on arterial smooth muscle, but also on heart muscle. In the heart, Ca2+ inward currents are important in generating depolarization of sinoatrial node cells (impulse generation), in impulse propagation through the AV- junction (atrioven-tricular conduction), and in electromechanical coupling in the ventricular car-diomyocytes. Verapamil thus produces negative chrono-, dromo-, and inotropic effects.

Indications. Verapamil is used as an antiarrhythmic drug in supraventric-ular tachyarrhythmias. In atrial flutter or fibrillation, it is effective in reducing ventricular rate by virtue of inhibiting AV-conduction. Verapamil is also employed in the prophylaxis of angina pec-toris attacks (p. 308) and the treatment of hypertension (p. 312). Adverse effects: Because of verapamil's effects on the sinus node, a drop in blood pressure fails to evoke a reflex tachycardia. Heart rate hardly changes; bradycardia may even develop. AV-block and myocardial insufficiency can occur. Patients frequently complain of constipation.

Gallopamil (= methoxyverapamil) is closely related to verapamil in both structure and biological activity.

Diltiazem is a catamphiphilic ben-zothiazepine derivative with an activity profile resembling that of verapamil.

III. T-channel selective blockers. Ca2+-channel blockers, such as verapamil and mibefradil, may block both Land T-type Ca2+ channels. Mibefradil shows relative selectivity for the latter and is devoid of a negative inotropic effect; its therapeutic usefulness is compromised by numerous interactions with other drugs due to inhibition of cytochrome P450-dependent enzymes (CYP 1A2, 2D6 and, especially, 3A4).

Calcium Blockers And Cyp Enzymes

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