Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/108917
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dc.contributor.authorCarrapita, Jorge-
dc.contributor.authorAbrantes, Ana Margarida-
dc.contributor.authorCampelos, Sofia-
dc.contributor.authorGonçalves, Ana Cristina-
dc.contributor.authorCardoso, Dulce-
dc.contributor.authorRibeiro, Ana Bela Sarmento-
dc.contributor.authorRocha, Clara-
dc.contributor.authorSantos, Jorge Nunes-
dc.contributor.authorBotelho, Maria Filomena-
dc.contributor.authorTralhão, José Guilherme-
dc.contributor.authorFarges, Olivier-
dc.contributor.authorBarbosa, Jorge Maciel-
dc.date.accessioned2023-09-25T09:14:47Z-
dc.date.available2023-09-25T09:14:47Z-
dc.date.issued2016-10-11-
dc.identifier.issn2045-2322pt
dc.identifier.urihttps://hdl.handle.net/10316/108917-
dc.description.abstractIt was reported that prevention of acute portal overpressure in small-for-size livers by inflow modulation results in a better postoperative outcome. The aim is to investigate the impact of portal blood flow reduction by splenic artery ligation after major hepatectomy in a murine model. Forty-eight rats were subjected to an 85% hepatectomy or 85% hepatectomy and splenic artery ligation. Both groups were evaluated at 24, 48, 72 and 120 post-operative hours: liver function, regeneration and viability. All methods and experiments were carried out in accordance with Coimbra University guidelines. Splenic artery ligation produces viability increase after 24 h, induces a relative decrease in oxidative stress during the first 48 hours, allows antioxidant capacity increment after 24 h, which is reflected in a decrease of half-time normalized liver curve at 48 h and at 72 h and in an increase of mitotic index between 48 h and 72 h. Splenic artery ligation combined with 85% hepatectomy in a murine model, allows portal inflow modulation, promoting an increase in hepatocellular viability and regeneration, without impairing the function, probably by inducing a less marked elevation of oxidative stress at first 48 hours.pt
dc.language.isoengpt
dc.publisherSpringer Naturept
dc.relationStrategic Project PEst-C/SAU/UI3282/2013pt
dc.relationUID/NEU/04539/2013pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subject.meshAnimalspt
dc.subject.meshApoptosispt
dc.subject.meshCell Survivalpt
dc.subject.meshHepatectomypt
dc.subject.meshHepatocytespt
dc.subject.meshLigationpt
dc.subject.meshLiverpt
dc.subject.meshLiver Function Testspt
dc.subject.meshLiver Regenerationpt
dc.subject.meshMalept
dc.subject.meshMembrane Potential, Mitochondrialpt
dc.subject.meshNecrosispt
dc.subject.meshOxidative Stresspt
dc.subject.meshPrimary Cell Culturept
dc.subject.meshRatspt
dc.subject.meshRats, Wistarpt
dc.subject.meshSpleenpt
dc.subject.meshSplenic Arterypt
dc.subject.meshSuperoxidespt
dc.subject.meshSurvival Analysispt
dc.titleImpact of splenic artery ligation after major hepatectomy on liver function, regeneration and viabilitypt
dc.typearticle-
degois.publication.firstPage34731pt
degois.publication.issue1pt
degois.publication.titleScientific Reportspt
dc.peerreviewedyespt
dc.identifier.doi10.1038/srep34731pt
degois.publication.volume6pt
dc.date.embargo2016-10-11*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitINESC Coimbra – Institute for Systems Engineering and Computers at Coimbra-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0003-4185-7871-
crisitem.author.orcid0000-0002-4142-4841-
crisitem.author.orcid0000-0002-4724-1843-
crisitem.author.orcid0000-0001-7202-1650-
Appears in Collections:I&D IBILI - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais
I&D INESCC - Artigos em Revistas Internacionais
FMUC Medicina - Artigos em Revistas Internacionais
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