Labetalol: A Review of Its Pharmacology, Pharmacokinetics, Clinical Uses and Adverse Effects
- 8 July 1983
- journal article
- review article
- Published by Wiley in Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy
- Vol. 3 (4) , 193-217
- https://doi.org/10.1002/j.1875-9114.1983.tb03252.x
Abstract
Labetalol is a combined alpha- and beta-adenoceptor blocking agent for oral and intravenous use in the treatment of hypertension. It is a nonselective competitive antagonist at beta-adrenoceptors and a competitive antagonist of postsynaptic alpha1-adrenoceptors. Labetalol is more potent at beta than at alpha1 adrenoceptors in man; the ratio of beta-alpha antagonism is 3:1 after oral and 6.9:1 after intravenous administration. Labetalol is readily absorbed in man after oral administration, but the drug, which is lipid soluble, undergoes considerable hepatic first-pass metabolism and has an absolute bioavailability of approximately 25%. There are no active metabolites, and the elimination half-life of the drug is approximately 6 hours. Unlike conventional beta-adrenoceptor blocking drugs without intrinsic sympathomimetic activity, labetalol, when given acutely, produces a decrease in peripheral vascular resistance and blood pressure with little alteration in heart rate or cardiac output. However, like conventional beta-blockers, labetalol may influence the renin-angiotensin-aldosterone system and respiratory function. Clinical studies have shown that the antihypertensive efficacy of labetalol is superior to placebo and to diuretic therapy and is at least comparable to that of conventional beta-blockers, methyldopa, clonidine and various adrenergic neuronal blockers. Labetalol administered alone or with a diuretic is often effective when other antihypertensive regimens have failed. Studies have shown that labetalol is effective in the treatment of essential hypertension, renal hypertension, pheochromocytoma, pregnancy hypertension and hypertensive emergencies. In addition, preliminary studies indicate that labetalol may be of value in the management of ischemic heart disease. The most troublesome side effect of labetalol therapy is posture-related dizziness. Other reported side effects of the drug include gastrointestinal disturbances, tiredness, headache, scalp tingling, skin rashes, urinary retention and impotence. Side effects related to the beta-adrenoceptor blocking effect of labetalol, including asthma, heart failure and Raynaud's phenomenon, have been reported in rare instances.Keywords
This publication has 210 references indexed in Scilit:
- Labetalol in tetanusAnaesthesia, 1983
- Increased plasma concentrations of prostacyclin metabolite 6-keto-PGF1α in essential hypertensionThe American Journal of Cardiology, 1983
- Effects of beta-adrenergic blockade on plasma lipids: A double-blind randomized placebo-controlled multi-center comparison of labetalol and metoprolol in patients with hypertensionThe American Journal of Cardiology, 1982
- The determination of labetalol in plasma by high-performance liquid chromatography using fluorescence detectionJournal of Pharmacological Methods, 1981
- Alpha-Adrenergic Receptor SubtypesNew England Journal of Medicine, 1980
- Clinical pharmacology of the new beta-adrenergic blocking drugs. Part 11. Effects of oral labetalol in patients with both angina pectoris and hypertension: a preliminary experienceAmerican Heart Journal, 1980
- Clinical pharmacology of the new beta-adrenergic blocking drugs. Part 7. New horizons in beta-adrenoceptor blockade therapy: LabetalolAmerican Heart Journal, 1979
- A functional basis for classification of α-adrenergic receptorsLife Sciences, 1977
- The electrophysiology of propranolol in manAmerican Heart Journal, 1974
- Use of propranolol in conjunction with alpha receptor blocking drugs in pheochromocytomaThe American Journal of Cardiology, 1966