1. Academic Validation
  2. Calcitonin gene-related peptide receptor antagonist human CGRP-(8-37)

Calcitonin gene-related peptide receptor antagonist human CGRP-(8-37)

  • Am J Physiol. 1989 Feb;256(2 Pt 1):E331-5. doi: 10.1152/ajpendo.1989.256.2.E331.
T Chiba 1 A Yamaguchi T Yamatani A Nakamura T Morishita T Inui M Fukase T Noda T Fujita
Affiliations

Affiliation

  • 1 Third Department of Internal Medicine, Kobe University School of Medicine, Japan.
Abstract

From this study, we predicted that the human Calcitonin gene-related peptide (hCGRP) fragment hCGRP-(8-37) would be a selective antagonist for CGRP receptors but an agonist for Calcitonin (CT) receptors. In rat liver plasma membrane, where CGRP receptors predominate and CT appears to act through these receptors, hCGRP-(8-37) dose dependently displaced 125I-[Tyr0]rat CGRP binding. However, hCGRP-(8-37) had no effect on Adenylate Cyclase activity in liver plasma membrane. Furthermore, hCGRP-(8-37) inhibited Adenylate Cyclase activation induced not only by hCGRP but also by hCT. On the other hand, in LLC-PK1 cells, where Calcitonin receptors are abundant and CGRP appears to act via these receptors, the bindings of 125I-[Tyr0]rat CGRP and 125I-hCT were both inhibited by hCGRP-(8-37). In contrast to liver membranes, interaction of hCGRP-(8-37) with these receptors led to stimulation of adenosine 3',5'-cyclic monophosphate (cAMP) production in LLC-PK1 cells, and moreover, this fragment did not inhibit the increased production of cAMP induced not only by hCT but also by hCGRP. Thus hCGRP-(8-37) appears to be a useful tool for determining whether the action of CGRP as well as that of CT is mediated via specific CGRP receptors or CT receptors.

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