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Dynamic mechanisms of non-classical antagonism by competitive AT(1) receptor antagonists.
Lew, M J; Ziogas, J; Christopoulos, A.
Affiliation
  • Lew MJ; Department of Pharmacology, University of Melbourne, Victoria 3010, Australia. m.lew@pharmacology.unimelb.edu.au
Trends Pharmacol Sci ; 21(10): 376-81, 2000 Oct.
Article in En | MEDLINE | ID: mdl-11050317
ABSTRACT
Selective competitive angiotensin AT(1) receptor antagonists exhibit diverse patterns of antagonism of angiotensin-II-mediated responses in functional assays. These range from the classical parallel rightward shift of agonist concentration-response curves with no depression of the maximum response to an apparently straightforward insurmountable antagonism with complete depression of the maximum response and no rightward shift. This article reviews some earlier equilibrium-based models that have been used to explain the insurmountable antagonism, and suggests that a kinetic model might provide a more satisfactory account of the observations. Such a model might provide deeper insights into the pharmacology of G-protein-coupled receptors than the more popular equilibrium models.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Angiotensin II / Angiotensin Receptor Antagonists / Models, Chemical Limits: Animals Language: En Journal: Trends Pharmacol Sci Year: 2000 Type: Article Affiliation country: Australia
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Angiotensin II / Angiotensin Receptor Antagonists / Models, Chemical Limits: Animals Language: En Journal: Trends Pharmacol Sci Year: 2000 Type: Article Affiliation country: Australia