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Pharmacological characterization of melanocortin receptors in fish suggests an important role for ACTH

  • Tatjana Haitina*
  • , Janis Klovins
  • , Helgi B. Schiöth
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

Abstract

The melanocortin (MC) receptor subtypes have distinctive characteristic binding profiles. We found that the trout and Fugu MC4 receptors have similar affinity for α-MSH and β-MSH and a much higher affinity for ACTH than does the human MC4 receptor. The Fugu MC1 and the trout and Fugu MC5 receptors also have higher affinity for ACTH-derived peptides than α-, β-, or γ-MSH. It is tempting to speculate that ACTH-derived peptides may have played an important role as "original" ligands at the MC receptors, while the specificity of the different subtypes for the α-, β-, and γ-MSH peptides may have appeared at later stages during vertebrate evolution.

Original languageEnglish
Pages (from-to)337-339
Number of pages3
JournalAnnals of the New York Academy of Sciences
Volume1040
DOIs
Publication statusPublished - 2005

Keywords

  • ACTH
  • Evolution
  • GPCR
  • Melanocortin
  • MSH

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