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dc.contributor.author | Garcia, Nahuel Aquiles | es_ES |
dc.contributor.author | Moncayo-Arlandi, Javier | es_ES |
dc.contributor.author | Vázquez Sánchez, Alejandro | es_ES |
dc.contributor.author | Genoves, Patricia | es_ES |
dc.contributor.author | Calvo Saiz, Conrado Javier | es_ES |
dc.contributor.author | Millet Roig, José | es_ES |
dc.contributor.author | Martí, Nuria | es_ES |
dc.contributor.author | Aguado, Carmen | es_ES |
dc.contributor.author | Knecht, Erwin | es_ES |
dc.contributor.author | Valiente-Alandi, Iñigo | es_ES |
dc.contributor.author | Montero, Jose Anastasio | es_ES |
dc.contributor.author | Diez-Juan, Antonio | es_ES |
dc.contributor.author | Sepulveda Sanchis, Pilar | es_ES |
dc.date.accessioned | 2020-10-17T03:32:32Z | |
dc.date.available | 2020-10-17T03:32:32Z | |
dc.date.issued | 2017-05-09 | es_ES |
dc.identifier.issn | 1425-9524 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/152270 | |
dc.description.abstract | [EN] Background: Cardioplegic arrest is a common procedure for many types of cardiac surgery, and different formulations have been proposed to enhance its cardio-protective effect. Hydrogen sulfide is an important signaling molecule that has cardio-protective properties. We therefore studied the cardio-protective effect of hydrogen sulfide in cardiac cell culture and its potential therapeutic use in combination with cardioplegia formulations. Materials/Methods: We added hydrogen sulfide donor GYY4137 to HL-1 cells to study its protective effect in nutrient starved conditions. In addition, we tested the potential use of GYY4137 when it is added into two different cardioplegia formulations: Cardi-Braun (R) solution and del Nido solution in an ex vivo Langendorff perfused rat hearts model. Results: We observed that eight-hour pre-treatment with GYY4137 significantly suppressed apoptosis in nutrient-starved HL-1 cells (28% less compared to untreated cells; p<0.05), maintained ATP content, and reduced protein synthesis. In ex vivo experiments, Cardi-Braun (R) and del Nido cardioplegia solutions supplemented with GYY4137 significantly reduced the pro-apoptotic protein caspase-3 content and preserved ATP content. Furthermore, GYY4137 supplemented cardioplegia solutions decreased the S-(5-adenosyl)-L-methionine/S-(adenosyl)-L-homocysteine ratio, reducing the oxidative stress in cardiac tissue. Finally, heart beating analysis revealed the preservation of the inter-beat interval and the heart rate in del Nido cardioplegia solution supplemented with GYY4137. Conclusions: GYY4137 preconditioning preserved energetic state during starved conditions, attenuating the cardiomyocytes apoptosis in vitro. The addition of GYY4137 to cardioplegia solutions prevented apoptosis, ATP consumption, and oxidative stress in perfused rat hearts, restoring its electrophysiological status after cardiac arrest. These findings suggested that GYY4137 sulfide donor may improve the cardioplegia solution performance during cardiac surgery. | es_ES |
dc.description.sponsorship | Instituto de Salud Carlos III grants (PI10/743, PI13/0414) and RETICS RD12/0019/0025 co-funded by FEDER "Una Manera de Hacer Europa". AG. acknowledges a fellowship from Erasmus Mundus Eurotango Program. ADJ acknowledges support from the Ramon y Cajal program (RYC-2008-02378). P.S. acknowledges support from PI10/743, PI13/414 grants and the Miguel Servet I3SNS and RETICS Program (RD12/0025). We thank Dr Kenneth McCreath for helpful comments on the manuscript. | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | International Scientific Information, Inc. | es_ES |
dc.relation.ispartof | Annals of Transplantation | es_ES |
dc.rights | Reconocimiento - No comercial - Sin obra derivada (by-nc-nd) | es_ES |
dc.subject | Cardiac Surgical Procedures | es_ES |
dc.subject | Cardioplegic Solutions | es_ES |
dc.subject | Hydrogen Sulfide | es_ES |
dc.subject.classification | INGENIERIA MECANICA | es_ES |
dc.subject.classification | TECNOLOGIA ELECTRONICA | es_ES |
dc.title | Hydrogen Sulfide Improves Cardiomyocyte Function in a Cardiac Arrest Model | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.12659/AOT.901410 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//RYC-2008-02378/ES/RYC-2008-02378/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/ISCIII//PI10%2F743/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MINECO//PI13%2F00414/ES/Mecanismos moleculares y celulares de las células mesenquimales humanas y de las células cardiacas residentes del adulto en el entorno cardiaco isquémico y el nicho hematopoyético/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MINECO//RD12%2F0019%2F0025/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Ingeniería Electrónica - Departament d'Enginyeria Electrònica | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Servicio de Alumnado - Servei d'Alumnat | es_ES |
dc.description.bibliographicCitation | Garcia, NA.; Moncayo-Arlandi, J.; Vázquez Sánchez, A.; Genoves, P.; Calvo Saiz, CJ.; Millet Roig, J.; Martí, N.... (2017). Hydrogen Sulfide Improves Cardiomyocyte Function in a Cardiac Arrest Model. Annals of Transplantation. 22:285-295. https://doi.org/10.12659/AOT.901410 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.12659/AOT.901410 | es_ES |
dc.description.upvformatpinicio | 285 | es_ES |
dc.description.upvformatpfin | 295 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 22 | es_ES |
dc.identifier.pmid | 28484204 | es_ES |
dc.identifier.pmcid | PMC6248014 | es_ES |
dc.relation.pasarela | S\360554 | es_ES |
dc.contributor.funder | European Commission | es_ES |
dc.contributor.funder | European Regional Development Fund | es_ES |
dc.contributor.funder | Ministerio de Economía y Competitividad | es_ES |
dc.contributor.funder | Ministerio de Ciencia e Innovación | es_ES |