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Authordc.contributor.authorRodrigo Salinas, Ramón 
Authordc.contributor.authorPrieto, Juan C. 
Authordc.contributor.authorCastillo, Rodrigo L. 
Admission datedc.date.accessioned2019-03-15T16:03:41Z
Available datedc.date.available2019-03-15T16:03:41Z
Publication datedc.date.issued2013
Cita de ítemdc.identifier.citationClinical Science, Volumen 124, Issue 1, 2018, Pages 1-15
Identifierdc.identifier.issn01435221
Identifierdc.identifier.other10.1042/CS20110663
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/165887
Abstractdc.description.abstractThe role of oxidative stress in ischaemic heart disease has been thoroughly investigated in humans. Increased levels of ROS (reactive oxygen species) and RNS (reactive nitrogen species) have been demonstrated during ischaemia and post-ischaemic reperfusion in humans. Depending on their concentrations, these reactive species can act either as benevolent molecules that promote cell survival (at low-to-moderate concentrations) or can induce irreversible cellular damage and death (at high concentrations). Although high ROS levels can induce NF-κB (nuclear factor κB) activation, inflammation, apoptosis or necrosis, low-to-moderate levels can enhance the antioxidant response, via Nrf2 (nuclear factor-erythroid 2-related factor 2) activation. However, a clear definition of these concentration thresholds remains to be established. Although a number of experimental studies have demonstrated that oxidative stress plays a major role in heart ischaemia/reperfusion pathophysiology, controlled clini
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceClinical Science
Keywordsdc.subjectAntioxidant
Keywordsdc.subjectApoptosis
Keywordsdc.subjectAutophagy
Keywordsdc.subjectIschaemia/reperfusion
Keywordsdc.subjectNecrosis
Keywordsdc.subjectOxidative stress
Títulodc.titleCardioprotection against ischaemia/reperfusion by vitamins C and E plus n-3 fatty acids: Molecular mechanisms and potential clinic applications
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile