Evaluation of bioenergetic and mitochondrial function in liver transplantation

Detalhes bibliográficos
Autor(a) principal: Martins, Rui Miguel
Data de Publicação: 2019
Outros Autores: Teodoro, João S., Furtado, Emanuel, Rolo, Anabela Pinto, Palmeira, Carlos Marques, Tralhão, José Guilherme
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/106860
https://doi.org/10.3350/cmh.2018.0087
Resumo: Background/Aims: We measured changes in mitochondrial function and bioenergetics that occur during ischemia/ reperfusion in fresh liver samples of patients undergoing liver transplantation. These variations correlated with markers of liver function and clinical outcome. Ischemia/reperfusion injury related to liver transplantation affects mitochondrial function and bioenergetics. Experimental studies were conducted to identify the role of bioenergetics and mitochondrial dysfunction. To the best of our knowledge, no investigation of these two factors’ impacts on liver transplantation has been performed. Methods: This was a prospective study of 28 patients who underwent liver transplantation. We measured parameters of mitochondrial function and bioenergetics in biopsies performed during the procedure. Results: We observed a statistically significant reduction in mitochondrial membrane potential, an increase in lag phase, and decreases in mitochondrial respiration and adenosine triphosphate content (P<0.010). Higher postoperative aminotransferase peaks correlated with worse mitochondrial function; mitochondrial respiration correlated with arterial lactate (P<0.010). Conclusions: There is a relationship between mitochondrial function and ischemia/reperfusion injury. The future use of these clinical markers as prognostic factors may allow early identification of post-transplant liver failure and may indicate the need to perform a new transplant. (Clin Mol Hepatol 2019;25:190-198)
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spelling Evaluation of bioenergetic and mitochondrial function in liver transplantationAdenosine triphosphate (ATP)MitochondriaIschemiaLiver extractsLiver transplantationAdenosine TriphosphateAdolescentAdultAgedAlanine TransaminaseAspartate AminotransferasesChildChild, PreschoolFemaleHumansInfantLiverMaleMembrane Potential, MitochondrialMiddle AgedMitochondriaProspective StudiesReperfusion InjuryYoung AdultLiver TransplantationBackground/Aims: We measured changes in mitochondrial function and bioenergetics that occur during ischemia/ reperfusion in fresh liver samples of patients undergoing liver transplantation. These variations correlated with markers of liver function and clinical outcome. Ischemia/reperfusion injury related to liver transplantation affects mitochondrial function and bioenergetics. Experimental studies were conducted to identify the role of bioenergetics and mitochondrial dysfunction. To the best of our knowledge, no investigation of these two factors’ impacts on liver transplantation has been performed. Methods: This was a prospective study of 28 patients who underwent liver transplantation. We measured parameters of mitochondrial function and bioenergetics in biopsies performed during the procedure. Results: We observed a statistically significant reduction in mitochondrial membrane potential, an increase in lag phase, and decreases in mitochondrial respiration and adenosine triphosphate content (P<0.010). Higher postoperative aminotransferase peaks correlated with worse mitochondrial function; mitochondrial respiration correlated with arterial lactate (P<0.010). Conclusions: There is a relationship between mitochondrial function and ischemia/reperfusion injury. The future use of these clinical markers as prognostic factors may allow early identification of post-transplant liver failure and may indicate the need to perform a new transplant. (Clin Mol Hepatol 2019;25:190-198)Korean Association for the Study of the Liver2019-06info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/106860http://hdl.handle.net/10316/106860https://doi.org/10.3350/cmh.2018.0087eng2287-27282287-285XMartins, Rui MiguelTeodoro, João S.Furtado, EmanuelRolo, Anabela PintoPalmeira, Carlos MarquesTralhão, José Guilhermeinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-04-27T10:36:48Zoai:estudogeral.uc.pt:10316/106860Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:23:15.427845Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Evaluation of bioenergetic and mitochondrial function in liver transplantation
title Evaluation of bioenergetic and mitochondrial function in liver transplantation
spellingShingle Evaluation of bioenergetic and mitochondrial function in liver transplantation
Martins, Rui Miguel
Adenosine triphosphate (ATP)
Mitochondria
Ischemia
Liver extracts
Liver transplantation
Adenosine Triphosphate
Adolescent
Adult
Aged
Alanine Transaminase
Aspartate Aminotransferases
Child
Child, Preschool
Female
Humans
Infant
Liver
Male
Membrane Potential, Mitochondrial
Middle Aged
Mitochondria
Prospective Studies
Reperfusion Injury
Young Adult
Liver Transplantation
title_short Evaluation of bioenergetic and mitochondrial function in liver transplantation
title_full Evaluation of bioenergetic and mitochondrial function in liver transplantation
title_fullStr Evaluation of bioenergetic and mitochondrial function in liver transplantation
title_full_unstemmed Evaluation of bioenergetic and mitochondrial function in liver transplantation
title_sort Evaluation of bioenergetic and mitochondrial function in liver transplantation
author Martins, Rui Miguel
author_facet Martins, Rui Miguel
Teodoro, João S.
Furtado, Emanuel
Rolo, Anabela Pinto
Palmeira, Carlos Marques
Tralhão, José Guilherme
author_role author
author2 Teodoro, João S.
Furtado, Emanuel
Rolo, Anabela Pinto
Palmeira, Carlos Marques
Tralhão, José Guilherme
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Martins, Rui Miguel
Teodoro, João S.
Furtado, Emanuel
Rolo, Anabela Pinto
Palmeira, Carlos Marques
Tralhão, José Guilherme
dc.subject.por.fl_str_mv Adenosine triphosphate (ATP)
Mitochondria
Ischemia
Liver extracts
Liver transplantation
Adenosine Triphosphate
Adolescent
Adult
Aged
Alanine Transaminase
Aspartate Aminotransferases
Child
Child, Preschool
Female
Humans
Infant
Liver
Male
Membrane Potential, Mitochondrial
Middle Aged
Mitochondria
Prospective Studies
Reperfusion Injury
Young Adult
Liver Transplantation
topic Adenosine triphosphate (ATP)
Mitochondria
Ischemia
Liver extracts
Liver transplantation
Adenosine Triphosphate
Adolescent
Adult
Aged
Alanine Transaminase
Aspartate Aminotransferases
Child
Child, Preschool
Female
Humans
Infant
Liver
Male
Membrane Potential, Mitochondrial
Middle Aged
Mitochondria
Prospective Studies
Reperfusion Injury
Young Adult
Liver Transplantation
description Background/Aims: We measured changes in mitochondrial function and bioenergetics that occur during ischemia/ reperfusion in fresh liver samples of patients undergoing liver transplantation. These variations correlated with markers of liver function and clinical outcome. Ischemia/reperfusion injury related to liver transplantation affects mitochondrial function and bioenergetics. Experimental studies were conducted to identify the role of bioenergetics and mitochondrial dysfunction. To the best of our knowledge, no investigation of these two factors’ impacts on liver transplantation has been performed. Methods: This was a prospective study of 28 patients who underwent liver transplantation. We measured parameters of mitochondrial function and bioenergetics in biopsies performed during the procedure. Results: We observed a statistically significant reduction in mitochondrial membrane potential, an increase in lag phase, and decreases in mitochondrial respiration and adenosine triphosphate content (P<0.010). Higher postoperative aminotransferase peaks correlated with worse mitochondrial function; mitochondrial respiration correlated with arterial lactate (P<0.010). Conclusions: There is a relationship between mitochondrial function and ischemia/reperfusion injury. The future use of these clinical markers as prognostic factors may allow early identification of post-transplant liver failure and may indicate the need to perform a new transplant. (Clin Mol Hepatol 2019;25:190-198)
publishDate 2019
dc.date.none.fl_str_mv 2019-06
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/106860
http://hdl.handle.net/10316/106860
https://doi.org/10.3350/cmh.2018.0087
url http://hdl.handle.net/10316/106860
https://doi.org/10.3350/cmh.2018.0087
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2287-2728
2287-285X
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Korean Association for the Study of the Liver
publisher.none.fl_str_mv Korean Association for the Study of the Liver
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
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