Recent insights into mitochondrial targeting strategies in liver transplantation
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10316/107689 https://doi.org/10.7150/ijms.22891 |
Resumo: | Ischemia/reperfusion (I/R) injury in liver transplantation can disrupt the normal activity of mitochondria in the hepatic parenchyma. This potential dysfunction of mitochondria after I/R injury could be responsible for the initial poor graft function or primary nonfunction observed after liver transplantation. Thus, determining the mechanisms that lead to human hepatic mitochondrial dysfunction might contribute to improving the outcome of liver transplantation. Furthermore, early identification of novel prognostic factors involved in I/R injury could serve as a key endpoint to predict the outcome of liver grafts and also to promote the early adoption of novel strategies that protect against I/R injury. Here, we briefly review recent advances in the study of mitochondrial dysfunction and I/R injury, particularly in relation to liver transplantation. Next, we highlight various pharmacological therapeutic strategies that could be applied, and discuss their relationship to relevant mitochondrion-related processes and targets. Lastly, we note that although considerable progress has been made in our understanding of I/R injury and mitochondrial dysfunction, further investigation is required to elucidate the cellular and molecular mechanisms underlying these processes, thereby identifying biomarkers that can help in evaluating donor organs. |
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Recent insights into mitochondrial targeting strategies in liver transplantationLiver transplantationMitochondriaIschemia/reperfusion injuryLiver preservation solutionPharmacological conditioningApoptosisHumansLiverLiver TransplantationMitochondriaProtective AgentsReperfusion InjuryIschemia/reperfusion (I/R) injury in liver transplantation can disrupt the normal activity of mitochondria in the hepatic parenchyma. This potential dysfunction of mitochondria after I/R injury could be responsible for the initial poor graft function or primary nonfunction observed after liver transplantation. Thus, determining the mechanisms that lead to human hepatic mitochondrial dysfunction might contribute to improving the outcome of liver transplantation. Furthermore, early identification of novel prognostic factors involved in I/R injury could serve as a key endpoint to predict the outcome of liver grafts and also to promote the early adoption of novel strategies that protect against I/R injury. Here, we briefly review recent advances in the study of mitochondrial dysfunction and I/R injury, particularly in relation to liver transplantation. Next, we highlight various pharmacological therapeutic strategies that could be applied, and discuss their relationship to relevant mitochondrion-related processes and targets. Lastly, we note that although considerable progress has been made in our understanding of I/R injury and mitochondrial dysfunction, further investigation is required to elucidate the cellular and molecular mechanisms underlying these processes, thereby identifying biomarkers that can help in evaluating donor organs.Ivyspring International Publisher2018info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/107689http://hdl.handle.net/10316/107689https://doi.org/10.7150/ijms.22891eng1449-1907Martins, Rui MiguelTeodoro, João SoeiroFurtado, 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:RCAAP2023-07-27T09:28:24Zoai:estudogeral.uc.pt:10316/107689Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:24:00.651356Repositório 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 |
Recent insights into mitochondrial targeting strategies in liver transplantation |
title |
Recent insights into mitochondrial targeting strategies in liver transplantation |
spellingShingle |
Recent insights into mitochondrial targeting strategies in liver transplantation Martins, Rui Miguel Liver transplantation Mitochondria Ischemia/reperfusion injury Liver preservation solution Pharmacological conditioning Apoptosis Humans Liver Liver Transplantation Mitochondria Protective Agents Reperfusion Injury |
title_short |
Recent insights into mitochondrial targeting strategies in liver transplantation |
title_full |
Recent insights into mitochondrial targeting strategies in liver transplantation |
title_fullStr |
Recent insights into mitochondrial targeting strategies in liver transplantation |
title_full_unstemmed |
Recent insights into mitochondrial targeting strategies in liver transplantation |
title_sort |
Recent insights into mitochondrial targeting strategies in liver transplantation |
author |
Martins, Rui Miguel |
author_facet |
Martins, Rui Miguel Teodoro, João Soeiro Furtado, Emanuel Rolo, Anabela Pinto Palmeira, Carlos Marques Tralhão, José Guilherme |
author_role |
author |
author2 |
Teodoro, João Soeiro 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 Soeiro Furtado, Emanuel Rolo, Anabela Pinto Palmeira, Carlos Marques Tralhão, José Guilherme |
dc.subject.por.fl_str_mv |
Liver transplantation Mitochondria Ischemia/reperfusion injury Liver preservation solution Pharmacological conditioning Apoptosis Humans Liver Liver Transplantation Mitochondria Protective Agents Reperfusion Injury |
topic |
Liver transplantation Mitochondria Ischemia/reperfusion injury Liver preservation solution Pharmacological conditioning Apoptosis Humans Liver Liver Transplantation Mitochondria Protective Agents Reperfusion Injury |
description |
Ischemia/reperfusion (I/R) injury in liver transplantation can disrupt the normal activity of mitochondria in the hepatic parenchyma. This potential dysfunction of mitochondria after I/R injury could be responsible for the initial poor graft function or primary nonfunction observed after liver transplantation. Thus, determining the mechanisms that lead to human hepatic mitochondrial dysfunction might contribute to improving the outcome of liver transplantation. Furthermore, early identification of novel prognostic factors involved in I/R injury could serve as a key endpoint to predict the outcome of liver grafts and also to promote the early adoption of novel strategies that protect against I/R injury. Here, we briefly review recent advances in the study of mitochondrial dysfunction and I/R injury, particularly in relation to liver transplantation. Next, we highlight various pharmacological therapeutic strategies that could be applied, and discuss their relationship to relevant mitochondrion-related processes and targets. Lastly, we note that although considerable progress has been made in our understanding of I/R injury and mitochondrial dysfunction, further investigation is required to elucidate the cellular and molecular mechanisms underlying these processes, thereby identifying biomarkers that can help in evaluating donor organs. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018 |
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/10316/107689 http://hdl.handle.net/10316/107689 https://doi.org/10.7150/ijms.22891 |
url |
http://hdl.handle.net/10316/107689 https://doi.org/10.7150/ijms.22891 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1449-1907 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Ivyspring International Publisher |
publisher.none.fl_str_mv |
Ivyspring International Publisher |
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) |
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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 |
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1799134125877100544 |