Melanocortin-4 receptor mRNA expressed in sympathetic outflow neurons to brown adipose tissue

Neuroanatomical and functional evidence

C. Kay Song, Cheryl H. Vaughan, Erin Keen-Rhinehart, Ruth Babette Harris, Denis Richard, Timothy J. Bartness

Research output: Contribution to journalArticle

105 Citations (Scopus)

Abstract

A precise understanding of neural circuits controlling lipid mobilization and thermogenesis remains to be determined. We have been studying the sympathetic nervous system (SNS) contributions to white adipose tissue (WAT) lipolysis largely in Siberian hamsters. Central melanocortins are implicated in the control of the sympathetic outflow to WAT, and, moreover, the melanocortin 4 receptors (MC4-R) appear to be principally involved. We previously found that acute third ventricular melanotan II (MTII; an MC3/4-R agonist) injections increase sympathetic drive (norepinephrine turnover) to interscapular brown adipose tissue (IBAT) and IBAT temperature. Here we tested whether MC4-R mRNA is expressed in IBAT SNS outflow neurons using in situ hybridization for the former and injections of the transneuronal viral retrograde tract tracer, pseudorabies virus (PRV) into IBAT, for the latter. Significant numbers of double-labeled cells for PRV and MC4-R mRNA were found across the neuroaxis (mean of all brain sites ∼60%), including the hypothalamic paraventricular nucleus (PVH; ∼80%). Acute parenchymal MTII microinjections into the PVH of awake, freely-moving hamsters, using doses below those able to increase IBAT temperature when injected into the third ventricle, increased IBAT temperature for as long as 4 h, as measured by temperature transponders implanted below the tissue. Collectively, these data add significant support to the view that central melanocortins are important in controlling IBAT thermogenesis via the SNS innervation of this tissue, likely through the MC4-Rs.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology
Volume295
Issue number2
DOIs
StatePublished - Aug 1 2008
Externally publishedYes

Fingerprint

Receptor, Melanocortin, Type 4
Brown Adipose Tissue
Neurons
Messenger RNA
Sympathetic Nervous System
Melanocortins
Suid Herpesvirus 1
White Adipose Tissue
Temperature
Thermogenesis
Lipid Mobilization
Phodopus
Injections
Third Ventricle
Paraventricular Hypothalamic Nucleus
Lipolysis
Microinjections
Cricetinae
In Situ Hybridization
Norepinephrine

Keywords

  • In situ hybridization
  • Melanocortins
  • Pseudorabies virus
  • Siberian hamsters
  • Tract tracing

ASJC Scopus subject areas

  • Physiology
  • Physiology (medical)

Cite this

Melanocortin-4 receptor mRNA expressed in sympathetic outflow neurons to brown adipose tissue : Neuroanatomical and functional evidence. / Song, C. Kay; Vaughan, Cheryl H.; Keen-Rhinehart, Erin; Harris, Ruth Babette; Richard, Denis; Bartness, Timothy J.

In: American Journal of Physiology - Regulatory Integrative and Comparative Physiology, Vol. 295, No. 2, 01.08.2008.

Research output: Contribution to journalArticle

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abstract = "A precise understanding of neural circuits controlling lipid mobilization and thermogenesis remains to be determined. We have been studying the sympathetic nervous system (SNS) contributions to white adipose tissue (WAT) lipolysis largely in Siberian hamsters. Central melanocortins are implicated in the control of the sympathetic outflow to WAT, and, moreover, the melanocortin 4 receptors (MC4-R) appear to be principally involved. We previously found that acute third ventricular melanotan II (MTII; an MC3/4-R agonist) injections increase sympathetic drive (norepinephrine turnover) to interscapular brown adipose tissue (IBAT) and IBAT temperature. Here we tested whether MC4-R mRNA is expressed in IBAT SNS outflow neurons using in situ hybridization for the former and injections of the transneuronal viral retrograde tract tracer, pseudorabies virus (PRV) into IBAT, for the latter. Significant numbers of double-labeled cells for PRV and MC4-R mRNA were found across the neuroaxis (mean of all brain sites ∼60{\%}), including the hypothalamic paraventricular nucleus (PVH; ∼80{\%}). Acute parenchymal MTII microinjections into the PVH of awake, freely-moving hamsters, using doses below those able to increase IBAT temperature when injected into the third ventricle, increased IBAT temperature for as long as 4 h, as measured by temperature transponders implanted below the tissue. Collectively, these data add significant support to the view that central melanocortins are important in controlling IBAT thermogenesis via the SNS innervation of this tissue, likely through the MC4-Rs.",
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