Beta blockers, also spelled β-blockers, are a class of medications that are predominantly used to manage abnormal heart rhythms (arrhythmia), and to protect the heart from a second heart attack after a first heart attack (secondary prevention).[1] They are also widely used to treat high blood pressure, although they are no longer the first choice for initial treatment of most patients.[2]
Beta receptors are found on cells of the heart muscles, smooth muscles, airways, arteries, kidneys, and other tissues that are part of the sympathetic nervous system and lead to stress responses, especially when they are stimulated by epinephrine (adrenaline). Beta blockers interfere with the binding to the receptor of epinephrine and other stress hormones and weaken the effects of stress hormones.
In 1964, James Black[6] synthesized the first clinically significant beta blockers—propranolol and pronethalol; it revolutionized the medical management of angina pectoris[7] and is considered by many to be one of the most important contributions to clinical medicine and pharmacology of the 20th century.[8]
^ abcBarranger K, Vivian E, Peterson AM (2006). "Hypertension". In Arcangelo VP, Peterson AM (eds.). Pharmacotherapeutics for advanced practice: a practical approach. Lippincott Williams & Wilkins. p. 205. ISBN978-0-7817-5784-3. Retrieved September 7, 2010.
^"Sir James Black, OM". The Telegraph. March 23, 2010. Archived from the original on March 27, 2010. Retrieved March 25, 2010.
^van der Vring JA, Daniëls MC, Holwerda NJ, Withagen PJ, Schelling A, Cleophas TJ, Hendriks MG (June 1999). "Combination of calcium channel blockers and beta blockers for patients with exercise-induced angina pectoris: a double-blind parallel-group comparison of different classes of calcium channel blockers. The Netherlands Working Group on Cardiovascular Research (WCN)". Angiology. 50 (6): 447–454. doi:10.1177/000331979905000602. PMID10378820. S2CID21885509.