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Hydrogen Sulfide Improves Cardiomyocyte Function in a Cardiac Arrest Model

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Hydrogen Sulfide Improves Cardiomyocyte Function in a Cardiac Arrest Model

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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


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