TY - CHAP
T1 - Des-acyl ghrelin
T2 - A metabolically active peptide
AU - Delhanty, Patric J.
AU - Neggers, Sebastian J.
AU - Van Der Lely, Aart J.
PY - 2013
Y1 - 2013
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84925852166&partnerID=8YFLogxK
U2 - 10.1159/000346059
DO - 10.1159/000346059
M3 - Chapter
C2 - 23652397
AN - SCOPUS:84925852166
SN - 9783805599085
T3 - Endocrine Development
SP - 112
EP - 121
BT - The Ghrelin System
A2 - Benso, Andrea
A2 - Ghigo, Ezio
A2 - Granata, Riccarda
A2 - Casanueva, Felipe F.
ER -