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Ghrelin: Structure and Function

Physiological Reviews · 2005 · Vol. 85(2) · pp. 495–522
Masayasu KojimaKenji Kangawa

Abstract

Small synthetic molecules called growth hormone secretagogues (GHSs) stimulate the release of growth hormone (GH) from the pituitary. They act through the GHS-R, a G protein-coupled receptor whose ligand has only been discovered recently. Using a reverse pharmacology paradigm with a stable cell line expressing GHS-R, we purified an endogenous ligand for GHS-R from rat stomach and named it "ghrelin," after a word root ("ghre") in Proto-Indo-European languages meaning "grow." Ghrelin is a peptide hormone in which the third amino acid, usually a serine but in some species a threonine, is modified by a fatty acid; this modification is essential for ghrelin's activity. The discovery of ghrelin indicates that the release of GH from the pituitary might be regulated not only by hypothalamic GH-releasing hormone, but also by ghrelin derived from the stomach. In addition, ghrelin stimulates appetite by acting on the hypothalamic arcuate nucleus, a region known to control food intake. Ghrelin is orexigenic; it is secreted from the stomach and circulates in the bloodstream under fasting conditions, indicating that it transmits a hunger signal from the periphery to the central nervous system. Taking into account all these activities, ghrelin plays important roles for maintaining GH release and energy homeostasis in vertebrates.

Regulation of Appetite and ObesityBiochemical Analysis and Sensing TechniquesAdipose Tissue and MetabolismGhrelinOrexigenicEndocrinologyInternal medicineHypothalamusEnergy homeostasisAppetiteBiologyHormoneThreonine

MeSH terms

Amino Acid SequenceAnimalsHumansMolecular Sequence DataStructure-Activity RelationshipTissue DistributionPeptide HormonesGhrelin
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