Your browser doesn't support javascript.
loading
Ligand bias prevents class equality among beta-blockers.
Thanawala, Vaidehi J; Forkuo, Gloria S; Stallaert, Wayne; Leff, Paul; Bouvier, Michel; Bond, Richard.
Affiliation
  • Thanawala VJ; Department of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX, USA.
  • Forkuo GS; Department of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX, USA.
  • Stallaert W; Department of Biochemistry, Université de Montréal, Montréal, Quebec, Canada; Institute for Research in Immunology and Cancer, Université de Montréal, Montréal, Quebec, Canada.
  • Leff P; Consultant in Pharmacology, Cheshire, UK.
  • Bouvier M; Department of Biochemistry, Université de Montréal, Montréal, Quebec, Canada; Institute for Research in Immunology and Cancer, Université de Montréal, Montréal, Quebec, Canada.
  • Bond R; Department of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX, USA. Electronic address: rabond@uh.edu.
Curr Opin Pharmacol ; 16: 50-7, 2014 Jun.
Article in En | MEDLINE | ID: mdl-24681351
ß-Blockers are used for a wide range of diseases from hypertension to glaucoma. In some diseases/conditions all ß-blockers are effective, while in others only certain subgroups are therapeutically beneficial. The best-documented example for only a subset of ß-blockers showing clinical efficacy is in heart failure, where members of the class have ranged from completely ineffective, to drugs of choice for treating the disease. Similarly, ß-blockers were tested in murine asthma models and two pilot clinical studies. A different subset was found to be effective for this clinical indication. These findings call into question the current system of classifying these drugs. To consider 'ß-blockers', as a single class is misleading when considering their rigorous pharmacological definition and their appropriate clinical application.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Adrenergic, beta-2 / Adrenergic beta-Antagonists Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Curr Opin Pharmacol Journal subject: FARMACOLOGIA Year: 2014 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Adrenergic, beta-2 / Adrenergic beta-Antagonists Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Curr Opin Pharmacol Journal subject: FARMACOLOGIA Year: 2014 Document type: Article Affiliation country: Country of publication: