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Physiol. Rev. 85: 495-522, 2005; doi:10.1152/physrev.00012.2004
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Ghrelin: Structure and Function

Masayasu Kojima and Kenji Kangawa

Molecular Genetics, Institute of Life Science, Kurume University, Kurume, Fukuoka; Department of Biochemistry, National Cardiovascular Center Research Institute, Suita, Osaka; and Translational Research Center, Kyoto University Hospital, Kyoto, Japan

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.


Address for reprint requests and other correspondence: Address for reprint requests and other correspondence: M. Kojima, Molecular Genetics, Institute of Life Science, Kurume University, Hyakunenkouen 1–1, Kurume, Fukuoka 839–0864, Japan (E-mail: mkojima{at}lsi.kurume-u.ac.jp)




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The Physiology and Potential Clinical Applications of Ghrelin, a Novel Peptide Hormone
Mayo Clin. Proc., May 1, 2006; 81(5): 653 - 660.
[Abstract] [Full Text] [PDF]


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J EndocrinolHome page
P J D Delhanty, B C J van der Eerden, M van der Velde, C Gauna, H A P Pols, H Jahr, H Chiba, A J van der Lely, and J P T M van Leeuwen
Ghrelin and unacylated ghrelin stimulate human osteoblast growth via mitogen-activated protein kinase (MAPK)/phosphoinositide 3-kinase (PI3K) pathways in the absence of GHS-R1a
J. Endocrinol., January 1, 2006; 188(1): 37 - 47.
[Abstract] [Full Text] [PDF]


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ScienceHome page
J. V. Zhang, P.-G. Ren, O. Avsian-Kretchmer, C.-W. Luo, R. Rauch, C. Klein, and A. J. W. Hsueh
Obestatin, a Peptide Encoded by the Ghrelin Gene, Opposes Ghrelin's Effects on Food Intake
Science, November 11, 2005; 310(5750): 996 - 999.
[Abstract] [Full Text] [PDF]


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GutHome page
T L Peeters
Ghrelin: a new player in the control of gastrointestinal functions
Gut, November 1, 2005; 54(11): 1638 - 1649.
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J EndocrinolHome page
N Govoni, R De Iasio, C Cocco, A Parmeggiani, G Galeati, U Pagotto, C Brancia, M Spinaci, C Tamanini, R Pasquali, et al.
Gastric immunolocalization and plasma profiles of acyl-ghrelin in fasted and fasted-refed prepuberal gilts
J. Endocrinol., September 1, 2005; 186(3): 505 - 513.
[Abstract] [Full Text] [PDF]




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