Skip to main navigation Skip to search Skip to main content

Pharmacological comparison of rat and human melanocortin 3 and 4 receptors in vitro

  • Helgi B. Schiöth*
  • , Amin A. Bouifrouri
  • , Richard Rudzish
  • , Ruta Muceniece
  • , Hajime Watanobe
  • , Jarl E.S. Wikberg
  • , Dan Larhammar
  • *Corresponding author for this work
  • Uppsala University
  • International University of Health and Welfare

Research output: Contribution to journal › Article › peer-review

32 Citations (Scopus)

Abstract

The melanocortin 3 and 4 receptors are G-protein-coupled receptors found in the hypothalamus with important role in regulation of the energy balance. In this study, we performed pharmacological comparison of the rat and human melancortin (MC) 3 and MC4 receptors. We transiently expressed the genes for these receptors individually in a mammalian cell line and determined the binding affinities to several MSH peptides. The results showed no major difference between the rat and human MC3 receptors while the rat MC4 receptor had higher affinity to several peptides compared with the human MC4 receptor. NDP-, α-, β-, γ-MSH, ACTH(1-24), HS014 and MTII had from 5- to 34-fold higher affinity for the rat MC4 receptor, while SHU9119, HS024 and HS028 had similar affinity for both the MC4 receptors. Pharmacological species difference have earlier been reported for the MC1 and MC5 receptors but this is the first report showing important differences between the rat and human MC4 receptors.

Original languageEnglish
Pages (from-to)7-12
Number of pages6
JournalRegulatory Peptides
Volume106
Issue number1-3
DOIs
Publication statusPublished - 15 Jun 2002

Keywords

  • cAMP
  • HS014
  • Ligand binding
  • Melanocortin receptor subtypes
  • MSH
  • Rat
  • SHU9119

Fingerprint

Dive into the research topics of 'Pharmacological comparison of rat and human melanocortin 3 and 4 receptors in vitro'. Together they form a unique fingerprint.

Cite this