Document Detail


The calcitonin gene-related peptide (CGRP) receptor antagonist BIBN4096BS blocks CGRP and adrenomedullin vasoactive responses in the microvasculature.
MedLine Citation:
PMID:  15237099     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Calcitonin gene-related peptide (CGRP) is a potent microvascular dilator neuropeptide that is considered to play an essential role in neurogenic vasodilatation and in maintaining functional integrity in peripheral tissues. We have examined the effect of the nonpeptide CGRP antagonist BIBN4096BS on responses to CGRP and the structurally related peptide adrenomedullin, AM, in murine isolated aorta and mesentery preparations, and in the cutaneous microvasculature in vivo. We show for the first time that BIBN4096BS is an effective antagonist of CGRP and AM responses in the murine mesenteric and cutaneous microvasculature, and of CGRP in the murine aorta. After local administration, BIBN4096BS selectively inhibits the potentiation of microvascular permeability in the cutaneous microvasculature by CGRP and AM, with no effect on responses induced by other microvascular vasodilators. BIBN4096BS reversed both newly developed and established vasoactive responses induced by CGRP. The ability of CGRP to potentiate plasma extravasation was lost when coinjected with compound 48/80 (where mast cells would be activated to release proteases), but regained when soybean trypsin inhibitor was coinjected with compound 48/80. These results demonstrate that BIBN4096BS is a selective antagonist of responses induced by CGRP and AM in the mouse microvasculature, and CGRP in the mouse aorta. The ability of BIBN4096BS to block an established CGRP microvascular vasodilatation indicates that the sustained vasodilator activity of CGRP is due to the retention of the active intact peptide and the continued involvement of the CGRP receptor.
Authors:
A D Grant; C W Tam; Z Lazar; M K Shih; S D Brain
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Publication Detail:
Type:  In Vitro; Journal Article; Research Support, Non-U.S. Gov't     Date:  2004-07-05
Journal Detail:
Title:  British journal of pharmacology     Volume:  142     ISSN:  0007-1188     ISO Abbreviation:  Br. J. Pharmacol.     Publication Date:  2004 Aug 
Date Detail:
Created Date:  2004-07-30     Completed Date:  2005-08-04     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  7502536     Medline TA:  Br J Pharmacol     Country:  England    
Other Details:
Languages:  eng     Pagination:  1091-8     Citation Subset:  IM    
Copyright Information:
Copyright 2004 Nature Publishing Group
Affiliation:
Centre for Cardiovascular Biology & Medicine, New Hunt's House, King's College London, Guy's Campus, London SE1 1UL, U.K.
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MeSH Terms
Descriptor/Qualifier:
Adrenomedullin
Animals
Aorta / drug effects,  physiology
Female
Mesenteric Arteries / drug effects,  physiology
Mice
Microcirculation / drug effects*,  metabolism
Peptides / antagonists & inhibitors*
Piperazines / pharmacology*
Quinazolines / pharmacology*
Receptors, Calcitonin Gene-Related Peptide / antagonists & inhibitors*
Skin / blood supply
Trypsin Inhibitors / pharmacology
Vasodilation / physiology*
p-Methoxy-N-methylphenethylamine / pharmacology
Chemical
Reg. No./Substance:
0/BIBN 4096BS; 0/Peptides; 0/Piperazines; 0/Quinazolines; 0/Receptors, Calcitonin Gene-Related Peptide; 0/Trypsin Inhibitors; 148498-78-6/Adrenomedullin; 4091-50-3/p-Methoxy-N-methylphenethylamine
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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