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Profound and rapid reduction in body temperature induced by the melanocortin receptor agonists.

Abstract
The melanocortin receptor 4 (MC4R) plays a major role in body weight regulation and its agonist MTII has been widely used to study the role of MC4Rs in energy expenditure promotion and feeding reduction. Unexpectedly, we observed that intraperitoneal (i.p.) administration of MTII induced a rapid reduction in both body temperature and energy expenditure, which was independent of its effect on feeding and followed by a prolonged increase in energy expenditure. The rapid reduction was at least partly mediated by brain neurons since intracerebroventricular (icv) administration of alpha melanocyte-stimulating hormone, an endogenous melanocortin receptor agonist, produced a similar response. In addition, the body temperature-lowering effect of MTII was independent of the presence of MC4Rs, but in a similar fashion to the previously shown effect on body temperature by 5'AMP. Moreover, β-adrenergic receptors (β-ARs) were required for the recovery from low body temperature induced by MTII and further pharmacological studies showed that the MTII's effect on body temperature may be partially mediated by the vasopressin V1a receptors. Collectively, our results reveal a previously unappreciated role for the melanocortin pathway in rapidly lowering body temperature.
AuthorsYuanzhong Xu, Eun Ran Kim, Shengjie Fan, Yan Xia, Yong Xu, Cheng Huang, Qingchun Tong
JournalBiochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 451 Issue 2 Pg. 184-9 (Aug 22 2014) ISSN: 1090-2104 [Electronic] United States
PMID25065745 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2014 Elsevier Inc. All rights reserved.
Chemical References
  • MC4R protein, mouse
  • Peptides, Cyclic
  • Receptor, Melanocortin, Type 4
  • Receptors, Adrenergic, beta
  • Receptors, Vasopressin
  • melanotan-II
  • alpha-MSH
Topics
  • Animals
  • Body Temperature (drug effects, physiology)
  • Energy Metabolism (drug effects, physiology)
  • Mice
  • Mice, Knockout
  • Peptides, Cyclic (pharmacology)
  • Receptor, Melanocortin, Type 4 (agonists, deficiency, physiology)
  • Receptors, Adrenergic, beta (deficiency, genetics, physiology)
  • Receptors, Vasopressin (physiology)
  • alpha-MSH (analogs & derivatives, pharmacology)

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