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Evolution of β-blockers: from anti-anginal drugs to ligand-directed signalling
Sir James Black developed β-blockers, one of the most useful groups of drugs in use today. Not only are they being used for their original purpose to treat angina and cardiac arrhythmias, but they are also effective therapeutics for hypertension, cardiac failure, glaucoma, migraine and anxiety. Rece...
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Formato: | Texto |
Lenguaje: | English |
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Published By Elsevier In Association With The International Union Of Pharmacology
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081074/ https://www.ncbi.nlm.nih.gov/pubmed/21429598 http://dx.doi.org/10.1016/j.tips.2011.02.010 |
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author | Baker, Jillian G. Hill, Stephen J. Summers, Roger J. |
author_facet | Baker, Jillian G. Hill, Stephen J. Summers, Roger J. |
author_sort | Baker, Jillian G. |
collection | PubMed |
description | Sir James Black developed β-blockers, one of the most useful groups of drugs in use today. Not only are they being used for their original purpose to treat angina and cardiac arrhythmias, but they are also effective therapeutics for hypertension, cardiac failure, glaucoma, migraine and anxiety. Recent studies suggest that they might also prove useful in diseases as diverse as osteoporosis, cancer and malaria. They have also provided some of the most useful tools for pharmacological research that have underpinned the development of concepts such as receptor subtype selectivity, agonism and inverse agonism, and ligand-directed signalling bias. This article examines how β-blockers have evolved and indicates how they might be used in the future. |
format | Text |
id | pubmed-3081074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Published By Elsevier In Association With The International Union Of Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-30810742011-05-31 Evolution of β-blockers: from anti-anginal drugs to ligand-directed signalling Baker, Jillian G. Hill, Stephen J. Summers, Roger J. Trends Pharmacol Sci Review Sir James Black developed β-blockers, one of the most useful groups of drugs in use today. Not only are they being used for their original purpose to treat angina and cardiac arrhythmias, but they are also effective therapeutics for hypertension, cardiac failure, glaucoma, migraine and anxiety. Recent studies suggest that they might also prove useful in diseases as diverse as osteoporosis, cancer and malaria. They have also provided some of the most useful tools for pharmacological research that have underpinned the development of concepts such as receptor subtype selectivity, agonism and inverse agonism, and ligand-directed signalling bias. This article examines how β-blockers have evolved and indicates how they might be used in the future. Published By Elsevier In Association With The International Union Of Pharmacology 2011-04 /pmc/articles/PMC3081074/ /pubmed/21429598 http://dx.doi.org/10.1016/j.tips.2011.02.010 Text en © 2011 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Review Baker, Jillian G. Hill, Stephen J. Summers, Roger J. Evolution of β-blockers: from anti-anginal drugs to ligand-directed signalling |
title | Evolution of β-blockers: from anti-anginal drugs to ligand-directed signalling |
title_full | Evolution of β-blockers: from anti-anginal drugs to ligand-directed signalling |
title_fullStr | Evolution of β-blockers: from anti-anginal drugs to ligand-directed signalling |
title_full_unstemmed | Evolution of β-blockers: from anti-anginal drugs to ligand-directed signalling |
title_short | Evolution of β-blockers: from anti-anginal drugs to ligand-directed signalling |
title_sort | evolution of β-blockers: from anti-anginal drugs to ligand-directed signalling |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081074/ https://www.ncbi.nlm.nih.gov/pubmed/21429598 http://dx.doi.org/10.1016/j.tips.2011.02.010 |
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