Des-acyl ghrelin: A metabolically active peptide

Patric J. Delhanty, Sebastian J. Neggers, Aart J. Van Der Lely

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

96 Citations (Scopus)

Abstract

Unacylated ghrelin (UAG), or des-acyl ghrelin, is slowly fighting its way up into the field of interest that studies preproghrelin gene-encoded peptides. Long considered to be an inert degradation product of (acylated) ghrelin (AG), UAG nowadays emerges as an important hormone, separate from the other proghrelin-derived peptides, AG and obestatin. UAG appears to have its own receptor, and it can share this receptor with AG, under experimental conditions at least. An increasing number of studies suggest that UAG can act as a potent functional inhibitor of ghrelin. It can even strongly suppress ghrelin levels in obese human diabetic subjects. Moreover, UAG can improve postprandial glycemia, especially in those subjects in whom preprandial acylated ghrelin levels are high, which makes UAG, or UAG analogs strong potential candidates for the development of drugs for the treatment of metabolic disorders or other conditions in which elevated AG/UAG ratios occur, such as diabetes, obesity and Prader-Willi syndrome.

Original languageEnglish
Title of host publicationThe Ghrelin System
EditorsAndrea Benso, Ezio Ghigo, Riccarda Granata, Felipe F. Casanueva
Pages112-121
Number of pages10
DOIs
Publication statusPublished - 2013
Externally publishedYes

Publication series

NameEndocrine Development
Volume25
ISSN (Print)1421-7082
ISSN (Electronic)1662-2979

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