A life without hunger: The Ups (and downs) to modulating melanocortin-3 receptor signaling

Andrew A. Butler, Clemence Girardet, Maria Mavrikaki, James L. Trevaskis, Heather Macarthur, Daniel Marks, Susan A. Farr

Research output: Contribution to journalShort survey

9 Citations (Scopus)

Abstract

Melanocortin neurons conserve body mass in hyper- or hypo-caloric conditions by conveying signals from nutrient sensors into areas of the brain governing appetite and metabolism. In mice, melanocortin-3 receptor (MC3R) deletion alters nutrient partitioning independently of hyperphagia, promoting accumulation of fat over muscle mass. Enhanced rhythms in insulin and insulin-responsive metabolic genes during hypocaloric feeding suggest partial insulin resistance and enhanced lipogenesis. However, exactly where and how MC3Rs affect metabolic control to alter nutrient partitioning is not known. The behavioral phenotypes exhibited by MC3R-deficient mice suggest a contextual role in appetite control. The impact of MC3R-deficiency on feeding behavior when food is freely available is minor. However, homeostatic responses to hypocaloric conditioning involving increased expression of appetite-stimulating (orexigenic) neuropeptides, binge-feeding, food anticipatory activity (FAA), entrainment to nutrient availability and enhanced feeding-related motivational responses are compromised with MC3R-deficiency. Rescuing Mc3r transcription in hypothalamic and limbic neurons improves appetitive responses during hypocaloric conditioning while having minor effects on nutrient partitioning, suggesting orexigenic functions. Rescuing hypothalamic MC3Rs also restores responses of fasting-responsive hypothalamic orexigenic neurons in hypocaloric conditions, suggesting actions that sensitize fasting-responsive neurons to signals from nutrient sensors. MC3R signaling in ventromedial hypothalamic SF1(+ve) neurons improves metabolic control, but does not restore appetitive responses or nutrient partitioning. In summary, desensitization of fasting-responsive orexigenic neurons may underlie attenuated appetitive responses of MC3R-deficient mice in hypocaloric situations. Further studies are needed to identify the specific location(s) of MC3Rs controlling appetitive responses and partitioning of nutrients between fat and lean tissues.

Original languageEnglish (US)
Article number128
JournalFrontiers in Neuroscience
Volume11
Issue numberMAR
DOIs
StatePublished - Mar 16 2017

Fingerprint

Receptor, Melanocortin, Type 3
Hunger
Food
Neurons
Appetite
Fasting
Fats
Melanocortins
Insulin
Hyperphagia
Lipogenesis
Feeding Behavior
Neuropeptides
Insulin Resistance

Keywords

  • Appetite
  • Diabetes
  • Homeostasis
  • Hypothalamus
  • Limbic system
  • Metabolism
  • Neuropeptide
  • Obesity

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Butler, A. A., Girardet, C., Mavrikaki, M., Trevaskis, J. L., Macarthur, H., Marks, D., & Farr, S. A. (2017). A life without hunger: The Ups (and downs) to modulating melanocortin-3 receptor signaling. Frontiers in Neuroscience, 11(MAR), [128]. https://doi.org/10.3389/fnins.2017.00128

A life without hunger : The Ups (and downs) to modulating melanocortin-3 receptor signaling. / Butler, Andrew A.; Girardet, Clemence; Mavrikaki, Maria; Trevaskis, James L.; Macarthur, Heather; Marks, Daniel; Farr, Susan A.

In: Frontiers in Neuroscience, Vol. 11, No. MAR, 128, 16.03.2017.

Research output: Contribution to journalShort survey

Butler, AA, Girardet, C, Mavrikaki, M, Trevaskis, JL, Macarthur, H, Marks, D & Farr, SA 2017, 'A life without hunger: The Ups (and downs) to modulating melanocortin-3 receptor signaling', Frontiers in Neuroscience, vol. 11, no. MAR, 128. https://doi.org/10.3389/fnins.2017.00128
Butler, Andrew A. ; Girardet, Clemence ; Mavrikaki, Maria ; Trevaskis, James L. ; Macarthur, Heather ; Marks, Daniel ; Farr, Susan A. / A life without hunger : The Ups (and downs) to modulating melanocortin-3 receptor signaling. In: Frontiers in Neuroscience. 2017 ; Vol. 11, No. MAR.
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