Adrenomedullin inhibits feeding in the rat by a mechanism involving calcitonin gene-related peptide receptors

Endocrinology. 1996 Aug;137(8):3260-4. doi: 10.1210/endo.137.8.8754748.

Abstract

The central effect of adrenomedullin on feeding was investigated in fasted rats. After intracerebroventricular administration, adrenomedullin decreased 2-h food intake in a dose-dependent manner. A dose of 1.7 nmol adrenomedullin decreased 2-h food intake by 57%. Adrenomedullin shares sequence homology with calcitonin gene-related peptide (CGRP), a central anorectic agent, and binding sites for both are present in the hypothalamus. Adrenomedullin competed for [125I]adrenomedullin- and [125I]CGRP-binding sites in hypothalamic membranes. The Kd for the [125I]adrenomedullin-binding site was 0.54 +/- 0.07 nM, with a binding capacity of 214 +/- 27 fmol/mg membrane protein (n = 3). CGRP and the CGRP receptor antagonist CGRP-(8-37) at concentrations up to 1 microM did not compete at these sites. The Kd for the CGRP-binding site was 0.10 +/- 0.02 nM, with a binding capacity of 250 +/- 31 fmol/mg, and the Ki values for adrenomedullin and CGRP-(8-37) were 4.6 +/- 2.1 and 4.0 +/- 1.6 nM, respectively (n = 3). Thus, adrenomedullin showed high affinity binding at both adrenomedullin- and CGRP-binding sites. To establish whether adrenomedullin reduces feeding via CGRP receptors, we coadministered adrenomedullin (1.7 nmol) and CGRP-(8-37) (30 nmol). The reduction in 2-h food intake induced by adrenomedullin was 50% inhibited by CGRP-(8-37). These results show that adrenomedullin decreases food intake in the rat, and this effect is mediated at least in part via CGRP receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenomedullin
  • Animals
  • Antihypertensive Agents / pharmacology
  • Binding, Competitive
  • Calcitonin Gene-Related Peptide / metabolism
  • Calcitonin Gene-Related Peptide / pharmacology
  • Dose-Response Relationship, Drug
  • Eating / drug effects*
  • Humans
  • Injections, Intraventricular
  • Male
  • Peptide Fragments / metabolism
  • Peptide Fragments / pharmacology
  • Peptides / antagonists & inhibitors
  • Peptides / metabolism
  • Peptides / pharmacology*
  • Rats
  • Rats, Wistar
  • Receptors, Calcitonin Gene-Related Peptide / physiology*

Substances

  • Antihypertensive Agents
  • Peptide Fragments
  • Peptides
  • Receptors, Calcitonin Gene-Related Peptide
  • calcitonin gene-related peptide (8-37)
  • Adrenomedullin
  • Calcitonin Gene-Related Peptide