C. Kamei et al., EPILEPTOGENIC ACTIVITY-INDUCED BY COMBINED TREATMENT WITH ANTIINFLAMMATORY DRUGS AND ENOXACIN AND ITS INHIBITION BY A CALCIUM-ANTAGONIST, NICARDIPINE, Methods and findings in experimental and clinical pharmacology, 18(9), 1996, pp. 579-588
Epileptogenic activity induced by combined treatment with antiinflamma
tory drugs and enoxacin was investigated in chronic electrode-implante
d rats. Ferubinac ethyl adn aspirin DL-lysine showed a spike or spike
and wave complex in EEG without showing remarkable behavioral changes
when they were injected intraventricularly, although a relatively high
dose was needed. Enoxacin, on the other hand, elicited potent epilept
ogenic activity characterized by uninterrupted high voltage spike and
wave complex at doses of 50 and 100 mu g. At the same time,rats showed
hyperactivity, jumping and violent convulsion. Combined treatment wit
h enoxacin (p.o.) and ferubinac ethyl (i.v.) caused potent epileptogen
ic activity characterized by uninterrupted burst of high voltage spike
and wave complex. Behaviorally, animals showed forelimb clonus, head
nodding and generalized convulsion. High voltage spike and wave comple
x was also observed after combined treatment with enoxacin (i. vent.)
and ferubinac ethyl (i.v. or i. vent) in association with hyperactivit
y and jumping and violent convulsion. Nicardipine remarkably inhibited
epileptic seizures induced by combined treatment with enoxacin (p.o)
and ferubinac ethyl (i.v.). It is concluded that simultaneous treatmen
t with enoxacin and ferubinac ethyl produced epileptogenic activity wh
en injected intraventricularly, and nicardipine inhibited convulsions
induced by combined use of enoxacin (p.o.) and ferubinac ethyl (i.v.).