Glucagon-like peptide-2 exhibits protective effect on hepatic ischemia-reperfusion injury in rats
dc.authorid | Yildirim, Sule/0000-0002-1815-808X | |
dc.contributor.author | Topaloglu, Naci | |
dc.contributor.author | Kucuk, Adem | |
dc.contributor.author | Yildirim, Sule | |
dc.contributor.author | Tekin, Mustafa | |
dc.contributor.author | Erdem, Havva | |
dc.contributor.author | Deniz, Mustafa | |
dc.date.accessioned | 2025-01-27T20:44:19Z | |
dc.date.available | 2025-01-27T20:44:19Z | |
dc.date.issued | 2015 | |
dc.department | Çanakkale Onsekiz Mart Üniversitesi | |
dc.description.abstract | Glucagon-like peptide-2 (GLP-2) has potent anti-inflammatory effects and protects against experimental ischemia/reperfusion (I/R) injury in pulmonary, intestinal, and myocardial tissue. However, its protective abilities against I/R injury in the liver are unknown. We investigated the potential role of GLP-2 pretreatment on hepatic I/R injury in rats. A total of 24 rats were randomly divided into three groups (n = 8). The first group was the control group; the second group was the vehicle-treated hepatic ischemia/reperfusion (HIR, vehicle saline-treated) group; and the third group was the GLP-2 pretreated I/R (GLP2-IR) group. Each rat in the third group was intraperitoneally administered 5 mu g GLP-2 for 5 d before the procedure. A portal triad was created to induce ischemia with a vascular atraumatic clamp. After 40 min, the clamp was released to initiate hepatic reperfusion for 6 h. Blood samples and tissue specimens from the liver were obtained. Alanine aminotransferase, aspartate aminotransferase, and total bilirubin levels significantly increased in the saline-treated HIR group (P < 0.001), whereas GLP-2 pretreatment significantly decreased their levels (P < 0.01). Our data suggested that GLP-2 pretreatment may have a protective effect on liver I/R injury. However, dose-response studies are necessary to determine the most effective dose. | |
dc.identifier.doi | 10.1007/s11684-015-0403-1 | |
dc.identifier.endpage | 373 | |
dc.identifier.issn | 2095-0217 | |
dc.identifier.issn | 2095-0225 | |
dc.identifier.issue | 3 | |
dc.identifier.pmid | 26290282 | |
dc.identifier.scopus | 2-s2.0-84973413830 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 368 | |
dc.identifier.uri | https://doi.org/10.1007/s11684-015-0403-1 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12428/24537 | |
dc.identifier.volume | 9 | |
dc.identifier.wos | WOS:000368445200012 | |
dc.identifier.wosquality | Q3 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | |
dc.publisher | Springer | |
dc.relation.ispartof | Frontiers of Medicine | |
dc.relation.publicationcategory | info:eu-repo/semantics/openAccess | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.snmz | KA_WoS_20250125 | |
dc.subject | ischemia/reperfusion | |
dc.subject | liver | |
dc.subject | glucagon-like peptide-2 | |
dc.subject | alanine aminotransferase | |
dc.title | Glucagon-like peptide-2 exhibits protective effect on hepatic ischemia-reperfusion injury in rats | |
dc.type | Article |