Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/26530
Title: Effects of centrally injected GLP-1 in various experimental models of gastric mucosal damage
Authors: Uludağ Üniversitesi/Tıp Fakültesi/Fizyoloji Anabilim Dalı.
0000-0003-0863-1547
İşbil, Naciye Büyükcoşkun
Güleç, Güldal
C-5730-2015
AAH-1692-2021
55665951400
6602752303
Keywords: Biochemistry and molecular biology
Endocrinology and metabolism
Pharmacology and pharmacy
GLP-1
Gastric mucosal damage
ICV
Glucagon-like peptide-1
Arterial-blood-pressure
Acid-secretion
Binding-sites
Rats
Brain
Amide
Expression
Ethanol
Ulcers
Issue Date: Jul-2004
Publisher: Elsevier Science
Citation: İşbil B. N. ve Güleç, G. (2004). “Effects of centrally injected GLP-1 in various experimental models of gastric mucosal damage”. Peptides, 25(7), 1179-1183.
Abstract: Glucagon-like peptide-1 (GLP-1) is accepted to be a peptide involved in the central regulation of gastrointestinal function, but its potential gastroprotective effect is not clear. The aim of this study was to investigate whether intracerebroventricularly injected GLP-1 has protective effects on gastric mucosal lesions induced by several models, and if yes, whether these effects are due to the gastric antisecretory effect of the peptide. GLP-1 which was injected in three different doses (1, 10, 100 ng/10 mul; i.c.v.) to conscious rats prevented the mucosal lesions induced by reserpine and ethanol, but did not prevent the gastric mucosal lesions induced by pyloric ligation. In addition, 1 ng/10 mul dose of centrally injected GLP-1 inhibited gastric acid secretion in pylorus-ligated rats. As a result, we conclude that intracerebroventricularly injected GLP-1 may play a role in the prevention of gastric mucosal lesions induced by certain experimental models and this gastroprotective effect may be independent from its antisecretory effect.
URI: https://doi.org/10.1016/j.peptides.2004.05.001
http://hdl.handle.net/11452/26530
ISSN: 0196-9781
https://www.sciencedirect.com/science/article/pii/S0196978104001822
Appears in Collections:Scopus
Web of Science

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