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Authordc.contributor.authorMaldonado Maldonado, Edio Luis
Authordc.contributor.authorRojas, Diego
Authordc.contributor.authorUrbina, Fabiola
Authordc.contributor.authorSolari Illescas, Aldo Gerónimo
Admission datedc.date.accessioned2021-10-28T17:26:11Z
Available datedc.date.available2021-10-28T17:26:11Z
Publication datedc.date.issued2021
Cita de ítemdc.identifier.citationAntioxidants 2021, 10, 1022es_ES
Identifierdc.identifier.other10.3390/antiox10071022
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/182471
Abstractdc.description.abstractChagas disease is a neglected tropical disease caused by the flagellated protozoa Trypanosome cruzi. This illness affects to almost 8-12 million people worldwide, however, is endemic to Latin American countries. It is mainly vectorially transmitted by insects of the Triatominae family, although other transmission routes also exist. T. cruzi-infected cardiomyocytes at the chronic stage of the disease display severe mitochondrial dysfunction and high ROS production, leading to chronic myocardial inflammation and heart failure. Under cellular stress, cells usually can launch mitochondrial biogenesis in order to restore energy loss. Key players to begin mitochondrial biogenesis are the PGC-1 (PPAR gamma coactivator 1) family of transcriptional coactivators, which are activated in response to several stimuli, either by deacetylation or dephosphorylation, and in turn can serve as coactivators for the NRF (nuclear respiratory factor) family of transcription factors. The NRF family of transcriptional activators, namely NRF1 and NRF2, can activate gene expression of oxidative phosphorylation (OXPHOS) components, mitochondrial transcriptional factor (Tfam) and nuclear encoded mitochondrial proteins, leading to mitochondrial biogenesis. On the other hand, NRF2 can activate gene expression of antioxidant enzymes in response to antioxidants, oxidants, electrophile compounds, pharmaceutical and dietary compounds in a mechanism dependent on KEAP1 (Kelch-like ECH-associated protein 1). Since a definitive cure to treat Chagas disease has not been found yet; the use of antioxidants a co-adjuvant therapy has been proposed in an effort to improve mitochondrial functions, biogenesis, and the antioxidant defenses response. Those antioxidants could activate different pathways to begin mitochondrial biogenesis and/or cytoprotective antioxidant defenses. In this review we discuss the main mechanisms of mitochondrial biogenesis and the NRF2-KEAP1 activation pathway. We also reviewed the antioxidants used as co-adjuvant therapy to treat experimental Chagas disease and their action mechanisms and finish with the discussion of antioxidant therapy used in Chagas disease patients.es_ES
Patrocinadordc.description.sponsorshipComision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) CONICYT FONDECYT 1190392 Instituto de Ciencias Biomedicas grant - Fondo Nacional de Desarrollo Cientifico y Tecnologico (FONDECYT) 1190392es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherMDPIes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
Sourcedc.sourceAntioxidantses_ES
Keywordsdc.subjectTrypanosoma cruzies_ES
Keywordsdc.subjectROSes_ES
Keywordsdc.subjectChagases_ES
Keywordsdc.subjectAntioxidantses_ES
Keywordsdc.subjectOxidative stresses_ES
Keywordsdc.subjectMitochondrial biogenesises_ES
Títulodc.titleThe use of antioxidants as potential co-adjuvants to treat chronic chagas diseasees_ES
Document typedc.typeArtículo de revistaes_ES
dc.description.versiondc.description.versionVersión publicada - versión final del editores_ES
dcterms.accessRightsdcterms.accessRightsAcceso abiertoes_ES
Catalogueruchile.catalogadorapces_ES
Indexationuchile.indexArtículo de publícación WoSes_ES


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