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dc.contributor.authorMeana González, Clara 
dc.contributor.authorRubín, José Manuel
dc.contributor.authorBordallo, Carmen
dc.contributor.authorSuárez, Lorena
dc.contributor.authorBordallo, Javier
dc.contributor.authorSánchez, Manuel
dc.date.accessioned2025-11-09T11:28:16Z
dc.date.available2025-11-09T11:28:16Z
dc.date.issued2015
dc.identifier.citationJournal of Cellular and Molecular Medicine, Feb 2016, vol. 20, n. 2, p. 302-12es
dc.identifier.issn1582-1838es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/79490
dc.descriptionProducción Científica
dc.description.abstractPolyamines contribute to several physiological and pathological processes, including cardiac hypertrophy in experimental animals. This involves an increase in ornithine decarboxylase (ODC) activity and intracellular polyamines associated with cyclic adenosine monophosphate (cAMP) increases. The aim of the study was to establish the role of these in the human heart in living patients. For this, polyamines (by high performance liquid chromatography) and the activity of ODC and N(1)-acetylpolyamine oxidases (APAO) were determined in the right atrial appendage of 17 patients undergoing extracorporeal circulation to correlate with clinical parameters. There existed enzymatic activity associated with the homeostasis of polyamines. Left atria size was positively associated with ODC (r = 0.661, P = 0.027) and negatively with APAO-N(1) -acetylspermine (r = -0.769, P = 0.026), suggesting that increased levels of polyamines are associated with left atrial hemodynamic overload. Left ventricular ejection fraction (LVEF) and heart rate were positively associated with spermidine (r = 0.690, P = 0.003; r = 0.590, P = 0.021) and negatively with N(1)-acetylspermidine (r = -0.554, P = 0.032; r = -0.644, P = 0.018). LVEF was negatively correlated with cAMP levels (r = -0.835, P = 0.001) and with cAMP/ODC (r = -0.794, P = 0.011), cAMP/spermidine (r = -0.813, P = 0.001) and cAMP/spermine (r = -0.747, P = 0.003) ratios. Abnormal LVEF patients showed decreased ODC activity and spermidine, and increased N(1) -acetylspermidine, and cAMP. Spermine decreased in congestive heart failure patients. The trace amine isoamylamine negatively correlated with septal wall thickness (r = -0.634, P = 0.008) and was increased in cardiac heart failure. The results indicated that modifications in polyamine homeostasis might be associated with cardiac function and remodelling. Increased cAMP might have a deleterious effect on function. Further studies should confirm these findings and the involvement of polyamines in different stages of heart failure.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherWiley
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.rights.uriAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectBioquímica
dc.subjectCardiología
dc.subjectFisiología humana
dc.subjectPatología clínica
dc.subject.classificationcorazón
dc.subject.classificationaurículas
dc.subject.classificationornitina descarboxilasa
dc.subject.classificationN1-acetilpoliamina oxidasa
dc.subject.classificationpoliaminas
dc.subject.classificationputrescina
dc.subject.classificationespermidina
dc.subject.classificationespermina
dc.subject.classificationAMP cíclico
dc.subject.classificationinsuficiencia cardíaca
dc.titleCorrelation between endogenous polyamines in human cardiac tissues and clinical parameters in patients with heart failurees
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2015 The Author(s)
dc.identifier.doi10.1111/jcmm.12674es
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/10.1111/jcmm.12674
dc.identifier.publicationfirstpage302es
dc.identifier.publicationissue2es
dc.identifier.publicationlastpage312es
dc.identifier.publicationtitleJournal of Cellular and Molecular Medicinees
dc.identifier.publicationvolume20es
dc.peerreviewedSIes
dc.identifier.essn1582-4934es
dc.rightsAttribution 4.0 International
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones
dc.subject.unesco2302 Bioquímica
dc.subject.unesco3205 Medicina Interna
dc.subject.unesco2411 Fisiología Humana


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