Relationship of α-MSH and AgRP axons to the perikarya of melanocortin-4 receptor neurons

Brain Res. 2019 Aug 15:1717:136-146. doi: 10.1016/j.brainres.2019.04.021. Epub 2019 Apr 19.

Abstract

The central melanocortin system is composed of neurons that express either the proopiomelanocortin (POMC) or the agouti-related protein (AgRP). POMC is cleaved in bioactive peptides, including the α-melanocyte-stimulating hormone (α-MSH). α-MSH activates the melanocortin-4 receptor (MC4R) inducing satiety, whereas AgRP acts as an inverse agonist of MC4R. However, only limited information is available regarding possible area-specific differences in the interaction between α-MSH and AgRP terminals on MC4R-expressing cells. Therefore, the objective of the present study was to compare the distribution pattern of α-MSH and AgRP terminals on the perikarya of MC4R-expressing neurons. We performed a triple-label immunofluorescence reaction in brain series of MC4R-reporter mice to visualize MC4R-expressing neurons together with AgRP and α-MSH terminals. POMC and AgRP neurons project to areas that contain MC4R-expressing cells, although several brain nuclei exhibit AgRP and α-MSH terminals, but they do no express MC4R, while other brain areas contain MC4R-expressing cells and receive no apparent innervation of AgRP and POMC neurons. AgRP terminals make more presumptive appositions than α-MSH on the soma of MC4R-expressing neurons of the medial preoptic area and paraventricular nucleus of the hypothalamus (Pa). Additionally, a higher percentage of MC4R cells receive at least one presumptive apposition from AgRP terminals in the median preoptic nucleus and Pa, compared to α-MSH appositions. Thus, our study revealed area-specific differences in the interaction between α-MSH and AgRP terminals and the soma of MC4R-expressing neurons. These findings provide new insights about the relationship between first- and second-order neurons of the central melanocortin system.

Keywords: Food intake; Hypothalamus; Leptin; Melanocortin system; POMC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agouti-Related Protein / metabolism*
  • Animals
  • Axons / metabolism
  • Brain / metabolism
  • Eating / physiology
  • Energy Metabolism / physiology
  • Hypothalamus / metabolism
  • Leptin / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neurons / metabolism
  • Paraventricular Hypothalamic Nucleus / metabolism
  • Receptor, Melanocortin, Type 4 / metabolism*
  • alpha-MSH / metabolism*

Substances

  • Agouti-Related Protein
  • Leptin
  • Receptor, Melanocortin, Type 4
  • alpha-MSH