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Article
Melanocortins and their receptors and antagonists
Current Drug Targets (2003)
  • J Voisey
  • L Carroll
  • A van Daal, Queensland University of Technology
Abstract
The melanocortins are a group of small protein hormones derived by post-translational cleavage of the proopiomelanocortin (POMC) gene product. The known melanocortin hormones include α-melanocyte stimulating hormone (MSH), β-MSH, γ-MSH and adrenocorticotropic hormone (ACTH). Five melanocortin receptors (MC1R through to MC5R) have been identified and most of these show tissue-specific expression patterns, as well as different binding affinities for each of the melanocortin hormones. The central melanocortin system consists of α-MSH, agouti-related protein (AGRP), MC3R and MC4R. AGRP and α-MSH are believed to be the natural antagonist and agonist respectively of MC3R and MC4R. This central melanocortin system is thought to play a fundamental role in the control of feeding and body weight. Knock-out mice models and genetic studies have pointed to the importance of the melanocortins in complex human pathways such as pigmentation, lipolysis, food intake, thermogenesis, sexual behaviour, memory and inflammatory response. Recently the melanocortins and their receptors have been the target for drug-based treatment of human physiological processes. MC3R and MC4R are likely targets for controlling body weight; MC1R may be used in the treatment of inflammation and MC2R for the treatment of glucocortical deficiency. A role for MC5R still remains unclear, but the evidence suggests an exocrine gland function.
Disciplines
Publication Date
October, 2003
Publisher Statement

Interim status: Citation only.

Voisey, J., Carroll, L., and van Daal, A. (2003) Melanocortins and their receptors and antagonists Current Drug Targets Vol. 4, Iss. 7, pp. 586-597.

Copyright ©Bentham Science Publishers Ltd, 2003.

Citation Information
J Voisey, L Carroll and A van Daal. "Melanocortins and their receptors and antagonists" Current Drug Targets Vol. 4 Iss. 7 (2003)
Available at: http://works.bepress.com/angela_v_daal/14/