| Literature DB >> 6089054 |
R Bernasconi, W Bencze, K Hauser, M Klein, P Martin, M Schmutz.
Abstract
GABA level and the activity of L-glutamate-1-decarboxylase (GAD) (EC 4.1.1.15) were studied in brains of mice treated with beta-vinyllactic acid, a new, selective and pyridoxal phosphate-independent GAD inhibitor. Valproate and diazepam protected mice against convulsions caused by beta-vinyllactic acid although both anti-epileptic drugs antagonized neither the decrease in GABA concentrations nor the inhibition of GAD observed after treatment with beta-vinyllactic acid alone. Assuming that the anticonvulsant effect measured with both antiepileptics is GABA mediated, these results support the hypothesis of a postsynaptic enhancement of GABAergic transmission by diazepam and valproate.Entities:
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Year: 1984 PMID: 6089054 DOI: 10.1016/0304-3940(84)90536-6
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046