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Arcuate nucleus (revision 4)

Old revision·16:07, 8 Oct 2024·DiagramDelphine

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Arcuate nucleus
LocationMediobasal hypothalamus, adjacent to the median eminence
Anorexigenic populationPOMC and CART neurons
Orexigenic populationAgRP and NPY neurons
Topic infobox · conventions

The arcuate nucleus is a region of the mediobasal hypothalamus containing two functionally opposed neuronal populations that regulate food intake: neurons expressing pro-opiomelanocortin (POMC), which suppress intake, and neurons expressing agouti-related peptide (AgRP) and neuropeptide Y, which promote it.[1]

Its position adjacent to the median eminence, where the capillaries are fenestrated, gives it unusual access to circulating signals. Hormones that cannot cross an intact blood-brain barrier can nonetheless influence arcuate neurons, which is why the nucleus is a principal target for peripherally administered peptides including GLP-1 receptor agonists.[1]

Neuronal populations

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POMC neurons synthesise a precursor that is cleaved to α-melanocyte-stimulating hormone and other products. Released α-MSH acts at melanocortin-3 and melanocortin-4 receptors on downstream neurons to suppress food intake. These neurons are activated by leptin, insulin and GLP-1 receptor signalling.[2][3]

AgRP/NPY neurons are activated by fasting and by ghrelin, and inhibited by leptin. AgRP is an inverse agonist at melanocortin-4 receptors — it does not merely block α-MSH but reduces constitutive receptor signalling below baseline — and NPY acts at its own receptors to promote feeding. The two populations also inhibit each other directly.

References

  1. ^ a b Schwartz MW, Woods SC, Porte D, Seeley RJ, Baskin DG. "Central nervous system control of food intake." Nature 404(6778):661–671 (2000). PMID 10766253.
  2. ^ Cone RD. "Anatomy and regulation of the central melanocortin system." Nature Neuroscience 8(5):571–578 (2005). DOI:10.1038/nn1455. PMID 15856065.
  3. ^ Woods SC. "The control of food intake: behavioral versus molecular perspectives." Cell Metabolism 9(6):489–498 (2009). PMID 19490904.