Show simple item record

dc.creatorARACENA,PAULA
dc.creatorAGUIRRE,PABLA
dc.creatorMUÑOZ,PABLO
dc.creatorNÚÑEZ,MARCO T
dc.date2006-01-01
dc.date.accessioned2019-05-02T21:21:30Z
dc.date.available2019-05-02T21:21:30Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0716-97602006000100017
dc.identifier.urihttp://revistaschilenas.uchile.cl/handle/2250/81629
dc.descriptionNeurons, as non-dividing cells, encounter a myriad of stressful conditions throughout their lifespan. In particular, there is increasing evidence that iron progressively accumulates in the brain with age and that iron-induced oxidative stress is the cause of several forms of neurodegeneration. Here, we review recent evidence that gives support to the following notions: 1) neuronal iron accumulation leads to oxidative stress and cell death; 2) neuronal survival to iron accumulation associates with decreased expression of the iron import transporter DMT1 and increased expression of the efflux transporter IREG1; and 3) the adaptive process of neurons towards iron-induced oxidative stress includes a marked increase in both the expression of the catalytic subunit of gamma glutamate-cysteine ligase and glutathione. These findings may help to understand aging-related neurodegeneration hallmarks: oxidative damage, functional impairment and cell death.
dc.formattext/html
dc.languageen
dc.publisherSociedad de Biología de Chile
dc.relation10.4067/S0716-97602006000100017
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceBiological Research v.39 n.1 2006
dc.subjectneurons
dc.subjectiron metabolism
dc.subjectiron accumulation
dc.subjectoxidative stress
dc.subjectglutathione metabolism
dc.subjectneurodegeneration
dc.titleIron and glutathione at the crossroad of redox metabolism in neurons


This item appears in the following Collection(s)

Show simple item record