Please use this identifier to cite or link to this item:
https://hdl.handle.net/10316/107693
DC Field | Value | Language |
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dc.contributor.author | Panisello-Roselló, Arnau | - |
dc.contributor.author | Alva, Norma | - |
dc.contributor.author | Flores, Marta | - |
dc.contributor.author | Lopez, Alexandre | - |
dc.contributor.author | Castro Benítez, Carlos | - |
dc.contributor.author | Folch-Puy, Emma | - |
dc.contributor.author | Rolo, Anabela | - |
dc.contributor.author | Palmeira, Carlos | - |
dc.contributor.author | Adam, René | - |
dc.contributor.author | Carbonell, Teresa | - |
dc.contributor.author | Roselló-Catafau, Joan | - |
dc.date.accessioned | 2023-07-27T10:02:43Z | - |
dc.date.available | 2023-07-27T10:02:43Z | - |
dc.date.issued | 2018-08-22 | - |
dc.identifier.issn | 1422-0067 | pt |
dc.identifier.uri | https://hdl.handle.net/10316/107693 | - |
dc.description.abstract | Institut George Lopez-1 (IGL-1) and Histidine-tryptophan-ketoglutarate (HTK) solutions are proposed as alternatives to UW (gold standard) in liver preservation. Their composition differs in terms of the presence/absence of oncotic agents such as HES or PEG, and is decisive for graft conservation before transplantation. This is especially so when fatty (steatotic) livers are used since these grafts are more vulnerable to ischemia insult during conservation. Their composition determines the extent of the subsequent reperfusion injury after transplantation. Aldehyde dehydrogenase-2 (ALDH2), a mitochondrial enzyme, has been reported to play a protective role in warm ischemia-reperfusion injury (IRI), but its potential in fatty liver cold ischemic injury has not yet been investigated. We evaluated the relevance of ALDH2 activity in cold ischemia injury when fatty liver grafts from Zucker Obese rats were preserved in UW, HTK, and IGL-1 solutions, in order to study the mechanisms involved. ALDH2 upregulation was highest in livers preserved in IGL-1. It was accompanied by a decrease in transaminases, apoptosis (Caspase 3 and TUNEL assay), and lipoperoxidation, which was concomitant with the effective clearance of toxic aldehydes such as 4-hydroxy-nonenal. Variations in ATP levels were also determined. The results were consistent with levels of NF-E2 p45-related factor 2 (Nrf2), an antioxidant factor. Here we report for the first time the relevance of mitochondrial ALDH2 in fatty liver cold preservation and suggest that ALDH2 could be considered a potential therapeutic target or regulator in clinical transplantation. | pt |
dc.description.sponsorship | This research was funded by Instituto de Salud Carlos III through FIS project PI 15/00110 co-funded by FEDER from Regional Development European Funds (European Union) and the FOIE GRAS project, which has received funding from the European Union’s Horizon 2020 Research and Innovation programme under the Marie Sklodowska-Curie Grant (Agreement No. 722619). | pt |
dc.language.iso | eng | pt |
dc.publisher | MDPI | pt |
dc.relation | info:eu-repo/grantAgreement/H2020/722619/EU/MarieSkłodowska-Curie/FOIEGRAS | pt |
dc.rights | openAccess | pt |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | pt |
dc.subject | ALDH2 | pt |
dc.subject | MDA | pt |
dc.subject | 4-hydroxynonenal (4-HNE) | pt |
dc.subject | caspases 3 | pt |
dc.subject | apoptosis | pt |
dc.subject | IGL-1 | pt |
dc.subject | UW | pt |
dc.subject | HTK | pt |
dc.subject.mesh | Aldehyde Dehydrogenase, Mitochondrial | pt |
dc.subject.mesh | Animals | pt |
dc.subject.mesh | Apoptosis | pt |
dc.subject.mesh | Biomarkers | pt |
dc.subject.mesh | Cryopreservation | pt |
dc.subject.mesh | Fatty Liver | pt |
dc.subject.mesh | Liver Transplantation | pt |
dc.subject.mesh | Mitochondria | pt |
dc.subject.mesh | Organ Preservation | pt |
dc.subject.mesh | Organ Preservation Solutions | pt |
dc.subject.mesh | Rats | pt |
dc.subject.mesh | Reactive Oxygen Species | pt |
dc.subject.mesh | Reperfusion Injury | pt |
dc.subject.mesh | Time Factors | pt |
dc.subject.mesh | Cold Ischemia | pt |
dc.title | Aldehyde Dehydrogenase 2 (ALDH2) in Rat Fatty Liver Cold Ischemia Injury | pt |
dc.type | article | - |
degois.publication.firstPage | 2479 | pt |
degois.publication.issue | 9 | pt |
degois.publication.title | International Journal of Molecular Sciences | pt |
dc.peerreviewed | yes | pt |
dc.identifier.doi | 10.3390/ijms19092479 | pt |
degois.publication.volume | 19 | pt |
dc.date.embargo | 2018-08-22 | * |
uc.date.periodoEmbargo | 0 | pt |
item.fulltext | Com Texto completo | - |
item.grantfulltext | open | - |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
item.openairetype | article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.project.grantno | FOIE GRAS -Bioenergetic Remodeling in the Pathophysiology and Treatment of Non-Alcoholic Fatty Liver Disease | - |
crisitem.author.researchunit | CNC - Center for Neuroscience and Cell Biology | - |
crisitem.author.orcid | 0000-0003-3535-9630 | - |
crisitem.author.orcid | 0000-0002-4833-2202 | - |
Appears in Collections: | I&D CNC - Artigos em Revistas Internacionais |
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File | Description | Size | Format | |
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Aldehyde-dehydrogenase-2-ALDH2-in-rat-fatty-liver-cold-ischemia-injuryInternational-Journal-of-Molecular-Sciences.pdf | 3.14 MB | Adobe PDF | View/Open |
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