Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/110189
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dc.contributor.authorCorreia, Sónia C.-
dc.contributor.authorCarvalho, Cristina-
dc.contributor.authorCardoso, Susana-
dc.contributor.authorSantos, Renato X.-
dc.contributor.authorSantos, Maria S.-
dc.contributor.authorOliveira, C. R.-
dc.contributor.authorPerry, George-
dc.contributor.authorZhu, Xiongwei-
dc.contributor.authorSmith, Mark A.-
dc.contributor.authorMoreira, Paula I.-
dc.date.accessioned2023-11-16T11:39:55Z-
dc.date.available2023-11-16T11:39:55Z-
dc.date.issued2010-
dc.identifier.issn16634365pt
dc.identifier.urihttps://hdl.handle.net/10316/110189-
dc.description.abstractMitochondria have long been known as the powerhouse of the cell. However, these organelles are also pivotal players in neuronal cell death. Mitochondrial dysfunction is a prominent feature of chronic brain disorders, including Alzheimer's disease (AD) and Parkinson's disease (PD), and cerebral ischemic stroke. Data derived from morphologic, biochemical, and molecular genetic studies indicate that mitochondria constitute a convergence point for neurodegeneration. Conversely, mitochondria have also been implicated in the neuroprotective signaling processes of preconditioning. Despite the precise molecular mechanisms underlying preconditioning-induced brain tolerance are still unclear, mitochondrial reactive oxygen species generation and mitochondrial ATP-sensitive potassium channels activation have been shown to be involved in the preconditioning phenomenon. This review intends to discuss how mitochondrial malfunction contributes to the onset and progression of cerebral ischemic stroke and AD and PD, two major neurodegenerative disorders. The role of mitochondrial mechanisms involved in the preconditioning-mediated neuroprotective events will be also discussed. Mitochondrial targeted preconditioning may represent a promising therapeutic weapon to fight neurodegeneration.pt
dc.language.isoengpt
dc.publisherFrontiers Media S.A.pt
dc.relationEuropean Foundation for the Study of Diabetes/Servier Programme 2007pt
dc.relationSFRH/BD/40702/2007pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectmitochondriapt
dc.subjectmitoKATP channelspt
dc.subjectneurodegenerationpt
dc.subjectneuroprotectionpt
dc.subjectpreconditioningpt
dc.subjectreactive oxygen speciespt
dc.titleMitochondrial preconditioning: a potential neuroprotective strategypt
dc.typearticle-
degois.publication.firstPage138pt
degois.publication.issueAUGpt
degois.publication.titleFrontiers in Aging Neurosciencept
dc.peerreviewedyespt
dc.identifier.doi10.3389/fnagi.2010.00138pt
degois.publication.volume2pt
dc.date.embargo2010-01-01*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0001-5887-6417-
crisitem.author.orcid0000-0002-9866-933X-
crisitem.author.orcid0000-0002-6881-9392-
crisitem.author.orcid0000-0001-6942-4328-
crisitem.author.orcid0000-0001-5177-6747-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
FCTUC Ciências da Vida - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais
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