Comparison of anticonvulsive and acute neuroprotective activity of three 2,3-benzodiazepine compounds, GYKI 52466, GYKI 53405, and GYKI 53655

GYKI 52466 [1-(4-aminophenyl)-4-methyl-7,8-methylenedioxy-5H-2,3-benzodiaze pine], a non-competitive AMPA [alpha -amino-3-hydroxy-5-methyl-4-isoxazolep ropionate] and kainate receptor antagonist and its two analogues, GYKI 5340 5 [1-(4-aminophenyl)-3-acetyl-4-methyl-3,4-dihydro-7,8-methylenedioxy-5H-2, 3-benzodiazepine] and GYKI 53655 [1-(4-aminophenyl)-3-methylcarbamyl-4-meth yl-3,4-dihydro-7,8-methylenedioxy-5H-2,3-benzodiazepine] were investigated in two seizure models and in MgCl2 induced global cerebral ischaemia, as an acute neuroprotective model. The ED50 values of GYKI 52466 for suppression of the tonic and clonic phases of sound-induced seizures were 3.6 and 4.3 mg/kg, respectively. The corresponding data for GYKI 53405 were 1.1 and 3.1 mg/kg, while ED50 values of GYKI 53655 were 1.3 and 2.0 mg/kg, respectivel y. The inhibition of seizure evoked by maximal electroshock was also found to be remarkable: the ED50 values of GYKI 52466 and its two analogues were 6.9, 2.6, and 2.2 mg/kg, respectively. All compounds prolonged the survival times in MgCl2 induced global cerebral ischaemia test in a close-dependent fashion, with PD50 (dose of 50% prolongation) values of 24.1, 8.3, and 8.2 mg/kg intraperitoneal respectively. In audiogenic seizure model the durati on of anticonvulsant action of 10 mg/kg GYKI 52466 and 5 mg/kg GYKI 53405, GYKI 53655 were examined, too. The effect of GYKI 52466 decreased to 50% af ter 2 h, while the analogues showed more than 80% seizure suppression 3 h a fter treatment. After 6 h the effect of GYKI 53655 decreased to zero, while the effect of GYKI 52466, remained on the 50% level. (C) 2001 Elsevier Sci ence Inc.