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http://purl.uniprot.org/citations/22464990http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22464990http://www.w3.org/2000/01/rdf-schema#comment"Methylmercury (MeHg) exposure at high concentrations poses significant neurotoxic threat to humans worldwide. The present study investigated the mechanisms of glutathione-mediated attenuation of MeHg neurotoxicity in primary cortical culture. MeHg (5 μM) caused depletion of mono- and disulfide glutathione in neuronal, glial and mixed cultures. Supplementation with exogenous glutathione, specifically glutathione monoethyl ester (GSHME) protected against the MeHg induced neuronal death. MeHg caused increased reactive oxygen species (ROS) formation measured by dichlorodihydrofluorescein (DCF) fluorescence with an early increase at 30 min and a late increase at 6h. This oxidative stress was prevented by the presence of either GSHME or the free radical scavenger, trolox. While trolox was capable of quenching the ROS, it showed no neuroprotection. Exposure to MeHg at subtoxic concentrations (3 μM) caused an increase in system x(c)(-) mediated (14)C-cystine uptake that was blocked by the protein synthesis inhibitor, cycloheximide (CHX). Interestingly, blockade of the early ROS burst prevented the functional upregulation of system x(c)(-). Inhibition of multidrug resistance protein-1 (MRP1) potentiated MeHg neurotoxicity and increased cellular MeHg. Taken together, these data suggest glutathione offers neuroprotection against MeHg toxicity in a manner dependent on MRP1-mediated efflux."xsd:string
http://purl.uniprot.org/citations/22464990http://purl.org/dc/terms/identifier"doi:10.1016/j.neuro.2012.03.004"xsd:string
http://purl.uniprot.org/citations/22464990http://purl.uniprot.org/core/author"Liu X."xsd:string
http://purl.uniprot.org/citations/22464990http://purl.uniprot.org/core/author"Petering D.H."xsd:string
http://purl.uniprot.org/citations/22464990http://purl.uniprot.org/core/author"Lobner D."xsd:string
http://purl.uniprot.org/citations/22464990http://purl.uniprot.org/core/author"Rush T."xsd:string
http://purl.uniprot.org/citations/22464990http://purl.uniprot.org/core/author"Nowakowski A.B."xsd:string
http://purl.uniprot.org/citations/22464990http://purl.uniprot.org/core/date"2012"xsd:gYear
http://purl.uniprot.org/citations/22464990http://purl.uniprot.org/core/name"Neurotoxicology"xsd:string
http://purl.uniprot.org/citations/22464990http://purl.uniprot.org/core/pages"476-481"xsd:string
http://purl.uniprot.org/citations/22464990http://purl.uniprot.org/core/title"Glutathione-mediated neuroprotection against methylmercury neurotoxicity in cortical culture is dependent on MRP1."xsd:string
http://purl.uniprot.org/citations/22464990http://purl.uniprot.org/core/volume"33"xsd:string
http://purl.uniprot.org/citations/22464990http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/22464990
http://purl.uniprot.org/citations/22464990http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/22464990
http://purl.uniprot.org/uniprot/#_A5D6P3-mappedCitation-22464990http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22464990
http://purl.uniprot.org/uniprot/#_O35379-mappedCitation-22464990http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22464990
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http://purl.uniprot.org/uniprot/#_Q9JL41-mappedCitation-22464990http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22464990
http://purl.uniprot.org/uniprot/#_Q8C7V6-mappedCitation-22464990http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22464990
http://purl.uniprot.org/uniprot/Q8BRD0http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22464990
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http://purl.uniprot.org/uniprot/O35379http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22464990