Monosodium l-glutamate-induced convulsions: changes in uptake and release of catecholamines in cerebral cortex and caudate nucleus of adult rats

Adult rats (60 days old) were injected intraperitoneally with 5 mg/g monosodium l-glutamate (MSG). During the convulsive period (1 h after injection), uptake and release of [ 3H]norepinephrine ( 3H-NE) and [ 14C]dopamine ( 14C-DA) were measured in a crude synaptosoma fraction and in slices of cerebr...

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Bibliographic Details
Published inEpilepsy research Vol. 4; no. 1; pp. 20 - 27
Main Authors Beas-Zárate, Carlos, Schliebs, Reinhard, Morales-Villagran, Alberto, Feria-Velasco, Alfredo
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.07.1989
Elsevier
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Summary:Adult rats (60 days old) were injected intraperitoneally with 5 mg/g monosodium l-glutamate (MSG). During the convulsive period (1 h after injection), uptake and release of [ 3H]norepinephrine ( 3H-NE) and [ 14C]dopamine ( 14C-DA) were measured in a crude synaptosoma fraction and in slices of cerebral cortex and caudate nucleus, respectively. A significant reduction of 3H-NE uptake was detected in cortical slices (by 42%) and in synaptosomal fraction (by 33%) of rats treated with MSG, whereas K +-stimulated 3H-NE release was decreased by 32% and 39% in brain slices and in a synaptosomal fraction of cerebral cortex, respectively, in comparison with animals injected with 0.9% NaCl aqueous solution (PSS). In the caudate nucleus, 14C-DA uptake was increased by 100% in brain slices and by 36% in the synaptosomal fraction following MSG administration, whereas K +-stimulated 14C-DA release was enhanced by 80% in slices and by 25% in synaptosomes as compared to PSS-injected rats. Data suggest that catecholaminergic neurotransmission may play an important role in the etiopathology of convulsions in the experimental model using MSG.
ISSN:0920-1211
1872-6844
DOI:10.1016/0920-1211(89)90054-5