Publication: Protective Effect of the Vasopressin Agonist Terlipressin in a Rat Model of Contrast-Induced Nephropathy
| dc.contributor.author | VELİOĞLU, ARZU | |
| dc.contributor.author | AŞICIOĞLU, EBRU | |
| dc.contributor.author | ARIKAN, İZZET HAKKI | |
| dc.contributor.author | ÖZEN ALAHDAB, YEŞİM | |
| dc.contributor.author | YILMAZ, YUSUF | |
| dc.contributor.author | TUĞLULAR, ZÜBEYDE SERHAN | |
| dc.contributor.authors | Ari, Elif; Yilmaz, Yusuf; Kedrah, Alla Elden; Alahdab, Yesim; Cakalagaoglu, Fulya; Arikan, Hakki; Kocak, Huseyin; Macunluoglu, Beyza; Atakan, Aydin; Kahveci, Arzu; Asicioglu, Ebru; Tuglular, Serhan; Ozener, Cetin | |
| dc.date.accessioned | 2022-03-12T17:51:46Z | |
| dc.date.accessioned | 2026-01-10T17:25:40Z | |
| dc.date.available | 2022-03-12T17:51:46Z | |
| dc.date.issued | 2011 | |
| dc.description.abstract | Background/Aims: Contrast-induced nephropathy (CIN) remains a leading cause of iatrogenic acute renal failure. Terlipressin, a long-acting analog of vasopressin, may improve renal function. This study aimed to investigate the possible protective effect of terlipressin against the development of experimental CIN in rats. Methods: Wistar albino rats (n = 32) were allocated randomly into four equal groups of 8 each, i.e. control, terlipressin, contrast media (CM), and terlipressin plus contrast media (TCM). CIN was induced by intravenous administration of indomethacin (10 mg/kg), N-nitro L-arginine methyl ester (L-NAME, 10 mg/kg, twice at 15 and 30 min), and high-osmolar contrast media meglumine amidotrizoate 60%. Renal function parameters, kidney histology, and tubular expression of vascular endothelial growth factor (VEGF) were determined. Results: Mean serum creatinine levels were decreased (p < 0.05) and creatinine clearance (p < 0.05) increased in the TCM group compared with the group. Notably, rats in the TCM group displayed less tubular necrosis (p < 0.05), medullary congestion (p < 0.05), and a reduced tubular expression of VEGF (p < 0.05) compared with the CM group. Conclusion: These results demonstrate that terlipressin can inhibit the development of CIN. Copyright (C) 2011 S. Karger AG, Basel | |
| dc.identifier.doi | 10.1159/000324764 | |
| dc.identifier.eissn | 1421-9670 | |
| dc.identifier.issn | 0250-8095 | |
| dc.identifier.pubmed | 21372562 | |
| dc.identifier.uri | https://hdl.handle.net/11424/230330 | |
| dc.identifier.wos | WOS:000289236400014 | |
| dc.language.iso | eng | |
| dc.publisher | KARGER | |
| dc.relation.ispartof | AMERICAN JOURNAL OF NEPHROLOGY | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Contrast-induced nephropathy | |
| dc.subject | Terlipressin | |
| dc.subject | Acute renal failure | |
| dc.subject | ENDOTHELIAL GROWTH-FACTOR | |
| dc.subject | HEPATORENAL-SYNDROME | |
| dc.subject | KIDNEY INJURY | |
| dc.subject | THERAPY | |
| dc.subject | METAANALYSIS | |
| dc.subject | PREVENTION | |
| dc.subject | STRATEGIES | |
| dc.subject | CIRRHOSIS | |
| dc.subject | TRIALS | |
| dc.title | Protective Effect of the Vasopressin Agonist Terlipressin in a Rat Model of Contrast-Induced Nephropathy | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 276 | |
| oaire.citation.issue | 3 | |
| oaire.citation.startPage | 269 | |
| oaire.citation.title | AMERICAN JOURNAL OF NEPHROLOGY | |
| oaire.citation.volume | 33 |
