dc.creatorMaldonado Maldonado, Edio Luis
dc.creatorRojas, Diego
dc.creatorUrbina, Fabiola
dc.creatorSolari Illescas, Aldo Gerónimo
dc.date.accessioned2021-10-28T17:26:11Z
dc.date.accessioned2022-01-27T19:30:50Z
dc.date.available2021-10-28T17:26:11Z
dc.date.available2022-01-27T19:30:50Z
dc.date.created2021-10-28T17:26:11Z
dc.date.issued2021
dc.identifierAntioxidants 2021, 10, 1022
dc.identifier10.3390/antiox10071022
dc.identifierhttps://repositorio.uchile.cl/handle/2250/182471
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3310741
dc.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.
dc.languageen
dc.publisherMDPI
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/us/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States
dc.sourceAntioxidants
dc.subjectTrypanosoma cruzi
dc.subjectROS
dc.subjectChagas
dc.subjectAntioxidants
dc.subjectOxidative stress
dc.subjectMitochondrial biogenesis
dc.titleThe use of antioxidants as potential co-adjuvants to treat chronic chagas disease
dc.typeArtículos de revistas


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