Journal
BRAIN RESEARCH
Volume 1411, Issue -, Pages 17-27Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.brainres.2011.07.003
Keywords
Melanotan II; Siberian hamster; Melanocortin-4 receptor; HS024; Interscapular brown adipose tissue; Cyclo [beta-Ala-His-D-Phe-Arg-Trp-Glu]-NH2
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Funding
- NIH [R37 DK35254, F32 DK082143]
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The melanocortins (MC) can affect interscapular brown adipose tissue (IBAT) thermogenesis via its sympathetic nervous system (SNS) innervation. We chose a site of high MC4-receptor (MC4-R) mRNA co-localization with SNS outflow neurons to IBAT, the subzona incerta (subZI) to test whether IBAT thermogenesis could be increased or decreased. We first performed immunohistochemical characterization of the subZI and found neurons and/or fibers in this area positive for melanin concentrating hormone, oxytocin, arginine vasopressin, agouti-related protein and alpha-melanocyte stimulating hormone. Functional characterization of the subZI was tested via site-specific microinjections. The MC3/4-R agonist, melanotan II [MTII (0.025, 0.05 and 0.075 nmol)], and specific MC4-R agonist (cyclo [beta-Ala-His-D-Phe-Arg-Trp-Glu]-NH2; 0.024 nmol) both significantly increased IBAT temperature (T-IBAT) and pretreatment with the MC4R antagonist, HS024 (0.072 nmol) blocked the MC4-R agonist-induced increased T-IBAT in conscious, freely-moving Siberian hamsters. Injection of the MC4-R antagonist alone significantly decreased T-IBAT up to 3 h post injection. Collectively, these results highlight the identification of a brain area that possesses high concentrations of MC4-R mRNA and SNS outflow neurons to IBAT that has not been previously reported to be involved in the control of T-IBAT. These results add to previously identified neural nodes that are components of the central circuits controlling thermogenesis. (C) 2011 Elsevier B.V. All rights reserved.
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