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Document type:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Article
Author(s):
Heppner, KM; Chaudhary, N; Müller, TD; Kirchner, H; Habegger, KM; Ottaway, N; Smiley, DL; DiMarchi, R; Hofmann, SM; Woods, SC; Sivertsen, B; Holst, B; Pfluger, PT; Perez-Tilve, D; Tschöp, MH
Title:
Acylation type determines ghrelin's effects on energy homeostasis in rodents.
Abstract:
Ghrelin is a gastrointestinal polypeptide that acts through the ghrelin receptor (GHSR) to promote food intake and increase adiposity. Activation of GHSR requires the presence of a fatty-acid (FA) side chain on amino acid residue serine 3 of the ghrelin molecule. However, little is known about the role that the type of FA used for acylation plays in the biological action of ghrelin. We therefore evaluated a series of differentially acylated peptides to determine whether alterations in length or...     »
Journal title abbreviation:
Endocrinology
Year:
2012
Journal volume:
153
Journal issue:
10
Pages contribution:
4687-95
Fulltext / DOI:
doi:10.1210/en.2012-1194
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/22865372
Print-ISSN:
0013-7227
TUM Institution:
Kliniken und Institute
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