Methylmercury increases glutamate release from brain synaptosomes and glutamate uptake by cortical slices from suckling rat pups: Modulatory effect of ebselen

被引:75
|
作者
Farina, M
Dahm, KCS
Schwalm, FD
Brusque, AM
Frizzo, MES
Zeni, G
Souza, DO
Rocha, JBT
机构
[1] Univ Fed Rio Grande do Sul, Dept Bioquim, Inst Ciencias Basicas Saude, BR-90035003 Porto Alegre, RS, Brazil
[2] Univ Estadual Rio Grande Sol, Curso Engn Bioproc & Biotecnol, Caxias Do Sul, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Dept Bioquim, Inst Ciencias Basicas Saude, BR-90035003 Porto Alegre, RS, Brazil
[4] Univ Fed Santa Maria, Dept Quim, Ctr Ciencias Nat & Exatas, BR-97105900 Santa Maria, RS, Brazil
[5] Univ Fed Rio Grande do Sul, Dept Ciencias Morfol, Inst Ciencias Basicas Saude, BR-90035003 Porto Alegre, RS, Brazil
关键词
methylmercury; ebselen; glutamate uptake; glutamate release; cortical slices; synaptosomes;
D O I
10.1093/toxsci/kfg058
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
During the early postnatal period the brain is extremely sensitive to external agents. Here, we examined the effect of subcutaneous injections of methylmercury (MeHg; 2 mg/kg) during the suckling period (postnatal days [PND] 3-10, 3-17, or 3-24) on glutamate release from brain synaptosomal preparations and on glutamate uptake by brain cortical slices of rat pups. The possible antagonist effect of ebselen against MeHg effect was also examined at PND 24. MeHg increased the basal (but not K+-stimulated) glutamate release and glutamate uptake at PND 24. A strong tendency of increase in the basal glutamate release from synaptosomes (p= 0.088) was observed at PND 17. Ebselen, which did not affect glutamate release and uptake per se, prevented both effects of MeHg. This study indicates that (1) the effect of MeHg on glutamate release could be involved in its toxicity; (2) the increase in the glutamate uptake could represent a pathophysiological response to MeHg-induced glutamate release; (3) the inhibitory effect of ebselen on MeHg-induced glutamate release could be related to its reported neuroprotective effects.
引用
收藏
页码:135 / 140
页数:6
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