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The melanocortin receptor subtypes in chicken have high preference to ACTH-derived peptides.


ABSTRACT: 1 Melanocortin (MC) receptors are widely distributed throughout the body of chicken, like in mammals, and participate in a wide range of physiological functions. 2 To clarify the pharmacological impact of ligands acting in the MC system, we expressed the chicken MC1, MC2, MC3, MC4 and MC5 (cMC1-5) receptors in eukaryotic cells and performed comprehensive pharmacological characterization of the potency of endogenous and synthetic melanocortin peptides. 3 Remarkably, the cMC receptors displayed high affinity for ACTH-derived peptides and in general low affinity for alpha-MSH. It is evident that not only the cMC2 receptor but also the other cMC receptors interact with ACTH-derived peptide through an epitope beyond the sequence of alpha-MSH. 4 The synthetic ligand MTII was found to be a potent agonist whereas HS024 was a potent antagonist at the cMC4 receptor, indicating that these ligands are suitable for physiological studies in chicken. 5 We also show the presence of prohormone convertase 1 (PC1) and PC2 genes in chicken, and that these peptides are coexpressed with proopiomelanocortin (POMC) in various tissues.

SUBMITTER: Ling MK 

PROVIDER: S-EPMC1575423 | biostudies-literature | 2004 Nov

REPOSITORIES: biostudies-literature

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The melanocortin receptor subtypes in chicken have high preference to ACTH-derived peptides.

Ling Maria K MK   Hotta Eri E   Kilianova Zuzana Z   Haitina Tatjana T   Ringholm Aneta A   Johansson Lisa L   Gallo-Payet Nicole N   Takeuchi Sakae S   Schiöth Helgi B HB  

British journal of pharmacology 20041004 5


1 Melanocortin (MC) receptors are widely distributed throughout the body of chicken, like in mammals, and participate in a wide range of physiological functions. 2 To clarify the pharmacological impact of ligands acting in the MC system, we expressed the chicken MC1, MC2, MC3, MC4 and MC5 (cMC1-5) receptors in eukaryotic cells and performed comprehensive pharmacological characterization of the potency of endogenous and synthetic melanocortin peptides. 3 Remarkably, the cMC receptors displayed hi  ...[more]

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