An unexpected molecular partnership within the brain neurons that regulate appetite has been identified in a new research.
The study, published by Cell Press in the January 26 issue of the journal Neuron, resolves a paradox regarding a receptor without its hormone and may lead to more specific therapeutic interventions for obesity and disorders of dopamine signaling.
Ghrelin is an appetite-stimulating hormone produced by the stomach. Although the ghrelin receptor (GHSR1a) is broadly distributed in the brain, ghrelin itself is nearly undetectable there. This intriguing paradox was investigated by Dr. Roy G. Smith, Dr. Andras Kern, and colleagues from The Scripps Research Institute in Florida. "We identified subsets of neurons in the brain that express both GHSR1a and the dopamine receptor subtype-2 (DRD2)," explains Dr. Smith. "Dopamine signaling in the hypothalamus is linked with feeding behavior, and mutations in DRD2 that attenuate dopamine signaling are associated with obesity in humans. We speculated that expression of both receptors in the same neurons might lead to interactions between GHSR1a and DRD2 that modify dopamine signaling."
"Perhaps most importantly, we showed that a GHSR1a-selective antagonist blocks dopamine signaling in neurons with both DRD2 and GHSR1a, which allows neuronal selective fine-tuning of dopamine signaling because neurons expressing DRD2 alone will be unaffected," concludes Dr. Smith. "This provides exciting opportunities for designing next-generation therapeutics with fewer side effects for both obesity and psychiatric disorders associated with abnormal dopamine signaling."