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Ethosuximide is an anticonvulsant.1,2,3,4,5 It increases glucose, fructose-1,6-bisphosphate, and pyruvate levels in rat brain when administered at a dose of 200 mg/kg.1 Ethosuximide (400 mg/kg) reduces the severity of audiogenic seizures in a rat model of barbiturate withdrawal-induced convulsions.2 It also inhibits tonic hindlimb extension induced by pentylenetetrazole (PTZ; Item No. 18682) or brainstem stimulation (ED50s = 35 and 70 mg/kg, respectively), as well as leptazol-induced clonic seizures (ED50 = 230 mg/kg), in rats.3,4 Ethosuximide reduces resting tremor by 60% in a macaque model of Parkinson's disease induced by MPTP when administered at a dose of 150 mg/animal for 5 days.5 Formulations containing ethosuximide have been used in the treatment of petit mal seizures.
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1. Biochemical effects of the anticonvulsants trimethadione, ethosuximide and chlordiazepoxide in rat brain. J. Neurochem. 19(8), 1937-1946 (1972).
2. The effects of drugs on barbiturate withdrawal convulsions in the rat. J. Pharm. Pharmacol. 22(10), 763-766 (1970).
3. Anticonvulsant interaction of cannabidiol and ethosuximide in rats. J. Pharm. Pharmacol. 29(8), 500-501 (1977).
4. The effect of anticonvulsant drugs on convulsions triggered by direct stimulation of the brainstem. Neuropharmacology 21(4), 355-359 (1982).
5. Effect of ethosuximide on rest tremor in the MPTP monkey model. Mov. Disord. 7(2), 137-141 (1992).