dc.creatorGlaser, Viviane
dc.creatorde Paula Martins, Roberta
dc.creatorHoffmann Vieira, Ana Julia
dc.creatorde Medeiros Oliveira, Eliana
dc.creatorStraliotto, Marcos Raniel
dc.creatorMukdsi, Jorge Humberto
dc.creatorTorres, Alicia Ines
dc.creatorFabro de Bem, Andreza
dc.creatorFarina, Marcelo
dc.creatorTeixeira da Rocha, Joao Batista
dc.creatorde Paul, Ana Lucia
dc.creatorLatini, Alexandra
dc.date.accessioned2018-01-16T17:41:34Z
dc.date.available2018-01-16T17:41:34Z
dc.date.created2018-01-16T17:41:34Z
dc.date.issued2014-03
dc.identifierGlaser, Viviane; de Paula Martins, Roberta; Hoffmann Vieira, Ana Julia; de Medeiros Oliveira, Eliana; Straliotto, Marcos Raniel; et al.; Diphenyl diselenide administration enhances cortical mitochondrial number and activity by increasing hemeoxygenase type 1 content in a methylmercury-induced neurotoxicity mouse model; Springer; Molecular and Cellular Biochemistry; 390; 1-2; 3-2014; 1-8
dc.identifier0300-8177
dc.identifierhttp://hdl.handle.net/11336/33427
dc.identifier1573-4919
dc.identifierCONICET Digital
dc.identifierCONICET
dc.description.abstractInterest in biochemistry of organoselenium compound has increased in the last decades, mainly due to their chemical and biological activities. Here, we investigated the protective effect of diphenyl diselenide (PhSe)2 (5 μmol/kg), in a mouse model of methylmercury (MeHg)-induced brain toxicity. Swiss male mice were divided into four experimental groups: control, (PhSe)2 (5 μmol/kg, subcutaneous administration), MeHg (40 mg/L, in tap water), and MeHg + (PhSe)2. After the treatment (21 days), the animals were killed and the cerebral cortex was analyzed. Electron microscopy indicated an enlarged and fused mitochondria leading to a reduced number of organelles, in the MeHg-exposed mice. Furthermore, cortical creatine kinase activity, a sensitive mitochondrial oxidative stress sensor, was almost abolished by MeHg. Subcutaneous (PhSe)2 co-treatment rescued from MeHg-induced mitochondrial alterations. (PhSe)2 also behaved as an enhancer of mitochondrial biogenesis, by increasing cortical mitochondria content in mouse-receiving (PhSe)2 alone. Mechanistically, (PhSe)2 (1 μM; 24 h) would trigger the cytoprotective Nrf-2 pathway for activating target genes, since astroglial cells exposed to the chalcogen showed increased content of hemeoxygenase type 1, a sensitive marker of the activation of this via. Thus, it is proposed that the (PhSe)2-neuroprotective effect might be linked to its mitoprotective activity.
dc.languageeng
dc.publisherSpringer
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1007/s11010-013-1870-9
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007%2Fs11010-013-1870-9
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectDiphenyl Diselenide
dc.subjectMethylmercury
dc.subjectMitochondrial Morphology
dc.subjectCreatine Kinase
dc.subjectHemeoxygenase Type 1
dc.titleDiphenyl diselenide administration enhances cortical mitochondrial number and activity by increasing hemeoxygenase type 1 content in a methylmercury-induced neurotoxicity mouse model
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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