dc.contributor.author | Sarıbaş, Gülistan Sanem | |
dc.contributor.author | Akçay, Neslihan Coşkun | |
dc.contributor.author | Akyol, Seda Nur | |
dc.contributor.author | Dayanır, Duygu | |
dc.contributor.author | Abraheem, Khadeejah | |
dc.contributor.author | Bilge, Mustafa | |
dc.contributor.author | Kavutcu, Mustafa | |
dc.contributor.author | Özoğul, Candan | |
dc.date.accessioned | 2023-03-17T11:30:03Z | |
dc.date.available | 2023-03-17T11:30:03Z | |
dc.date.issued | 2020 | en_US |
dc.identifier.citation | Sarıbaş, G., Coşkun Akçay, N., Akyol, S., Dayanır, D., Abraheem, K., Bilge, M., ... & Özoğul, C. (2020). HTK-Alcar, a Modified Organ Transplantation Solution, Decreases Ischemic Injury in the Rat Kidney Tissue. GAZI MEDICAL JOURNAL, 31(4). | en_US |
dc.identifier.issn | 21472092 | |
dc.identifier.uri | https://doi.org/10.12996/GMJ.2020.143 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12513/4979 | |
dc.description.abstract | Objectives: Histidine-tryptophan-ketoglutarate (HTK) solution is the storage solution used in organ transplantation. However, such solutions cannot completely eliminate tissue damage. Acetyl L-carnitine (Alcar) is a strong antioxidant. In this study we aimed to determine the protective effects of HTK solution prepared with Alcar in kidney tissue. Methods: Twenty-four rats used in this study were divided into 4 groups. Kidneys of rats in groups 1 and 2 were stored for 4 hours in HTK and HTK+Alcar solutions, respectively. Kidneys of rats in groups 3 and 4 were stored for 24 hours in HTK and HTK+Alcar solutions, respectively. Histological and immunohistochemical examinations of the kidneys were performed. In addition, TUNEL analysis was performed for the evaluation of apoptosis. Results: The findings of histomorphological damage in short-term HTK and HTK+Alcar groups were mild, but it was found widely in long-term HTK and ong-term HTK+Alcar groups on histologic evaluation. When histological scoring was made from kidney sections stained with H&E, the scores in HTK+Alcar groups decreased significantly compared to HTK groups. It was also seen that the score level increased significantly in long-term groups. According to immunohistochemical evaluation, in short- and long-term HTK +Alcar groups, the acetyl-L-carnitine prevented the antiapoptotic mechanisms to be activated and the intense expression of Bcl-2 has not occurred. In short- and long-term HTK groups, osteopontin showed more immunopositive result. Conclusion: It was determined that the modified HTK solution prevented the increase of the activation of the expected oxidant mechanisms resulting in ischemia. This contribution of acetyl-L-carnitine was also found in long-term group findings. © Copyright 2020 by Gazi University Medical Faculty. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Gazi Universitesi | en_US |
dc.relation.isversionof | 10.12996/GMJ.2020.143 | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Acetyl L-carnitine | en_US |
dc.subject | Apoptosis | en_US |
dc.subject | Histidine-tryptophan-ketoglutarate | en_US |
dc.subject | Ischemia | en_US |
dc.subject | Kidney | en_US |
dc.title | HTK-Alcar, a modified organ transplantation solution, decreases ischemic injury in the rat kidney tissue | en_US |
dc.type | article | en_US |
dc.relation.journal | Gazi Medical Journal | en_US |
dc.contributor.department | Tıp Fakültesi | en_US |
dc.contributor.authorID | Gülistan Sanem Sarıbaş / 0000-0001-7582-6235 | en_US |
dc.identifier.volume | 31 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.startpage | 622 | en_US |
dc.identifier.endpage | 629 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |