Amifostine enhances the antioxidant and hepatoprotective effects of UW and HTK preservation solutions
dc.authorid | Dagdeviren, Attila/0000-0001-8990-8282 | |
dc.authorid | Oksuz, Ergun/0000-0002-5723-5965 | |
dc.authorid | Akbulut, Sami/0000-0002-6864-7711 | |
dc.authorid | Sevmis, Sinasi/0000-0001-8728-5472 | |
dc.authorid | BAYRAKTAR, NILUFER/0000-0002-7886-3688 | |
dc.authorwosid | Dagdeviren, Attila/P-2877-2014 | |
dc.authorwosid | Oksuz, Ergun/K-8238-2012 | |
dc.authorwosid | Akbulut, Sami/L-9568-2014 | |
dc.authorwosid | Dağdeviren, Attila/AES-7155-2022 | |
dc.authorwosid | Sevmis, Sinasi/JOZ-7660-2023 | |
dc.authorwosid | BAYRAKTAR, NILUFER/Y-8758-2018 | |
dc.contributor.author | Akbulut, Sami | |
dc.contributor.author | Sevmis, Sinasi | |
dc.contributor.author | Karakayali, Hamdi | |
dc.contributor.author | Bayraktar, Nilufer | |
dc.contributor.author | Unlukaplan, Muge | |
dc.contributor.author | Oksuz, Ergun | |
dc.contributor.author | Dagdeviren, Atilla | |
dc.date.accessioned | 2024-08-04T20:39:54Z | |
dc.date.available | 2024-08-04T20:39:54Z | |
dc.date.issued | 2014 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | AIM: To investigate whether amifostine contributes to the antioxidant and cytoprotective effects of histidine-tryptophan-ketoglutarate (HTK) and University of Wisconsin (UW) preservation solutions. METHODS: Forty-eight Sprague Dawley male rats were equally divided into six groups: (1) ringer Lactate (RL) group; (2) RL + amifostine (RL + A) group; (3) HTK group; (4) HTK + A group; (5) UW group; and (6) UW + A group. Rats in the RL + A, HTK + A and UW + A groups were administered amifostine intraperitoneally at a dose of 200 mg/kg prior to laparotomy. The RL group was perfused with RL into the portal vein. The RL + A group were perfused with RL into the portal vein after amifostine administration. The HTK group received an HTK perfusion while the HTK + A group received an HTK perfusion after administration of amifostine. The UW group received a perfusion of UW, while the UW + A group received a UW perfusion after amifostine administration. Liver biopsy was performed to investigate histopathological, immunochemical [transferase mediated dUTP nick end labeling (TUNEL), inducible nitric oxide syntetase (iNOS)] and ultrastructural alterations. Biochemical alterations were determined by examining levels of alanine aminotransferase, alkaline phosphatase and nitric oxide in the perfusion fluid. RESULTS: Pathological sinusoidal dilatation and centrilobular hydropic alteration were significantly lower in the groups that received amifostine prior to preservation solution perfusion. Although the best results were obtained in the UW + A group, we did not observe a statistically significant difference between the UW + A and HTK + A groups. iNOS grades were significantly lower in the amifostine groups 12 h after treatment. When the amifostine groups were compared against each other, the iNOS grades obtained from the UW + A and HTK + A groups were similar while the RL + A group had a much poorer score. TUNEL assays demonstrated a lower apoptosis ratio in the amifostine groups than in the non-amifostine groups 12 h after treatment. No statistically significant difference was observed between the UW + A and HTK + A groups for apoptosis. Cellular ultrastructure was best preserved in the UW + A and HTK + A groups. CONCLUSION: Here, we show that preoperative administration of a single dose of amifostine is sufficient to minimize the preservation damage in hepatic cells. (C) 2014 Baishideng Publishing Group Inc. All rights reserved. | en_US |
dc.identifier.doi | 10.3748/wjg.v20.i34.12292 | |
dc.identifier.endpage | 12300 | en_US |
dc.identifier.issn | 1007-9327 | |
dc.identifier.issn | 2219-2840 | |
dc.identifier.issue | 34 | en_US |
dc.identifier.pmid | 25232264 | en_US |
dc.identifier.scopus | 2-s2.0-84909609683 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.startpage | 12292 | en_US |
dc.identifier.uri | https://doi.org/10.3748/wjg.v20.i34.12292 | |
dc.identifier.uri | https://hdl.handle.net/11616/96588 | |
dc.identifier.volume | 20 | en_US |
dc.identifier.wos | WOS:000341719100038 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Baishideng Publishing Group Inc | en_US |
dc.relation.ispartof | World Journal of Gastroenterology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Liver | en_US |
dc.subject | Transplantation | en_US |
dc.subject | Preservation solutions | en_US |
dc.subject | Histidine-tryptophan-ketoglutarate | en_US |
dc.subject | University of Wisconsin | en_US |
dc.subject | Antioxidant | en_US |
dc.subject | Amifostine | en_US |
dc.title | Amifostine enhances the antioxidant and hepatoprotective effects of UW and HTK preservation solutions | en_US |
dc.type | Article | en_US |