Peterson S L, Schwade N D
Department of Medical Pharmacology and Toxicology, Texas A&M University, College Station 77843-1114.
Epilepsy Res. 1993 Jun;15(2):141-8. doi: 10.1016/0920-1211(93)90094-n.
D-Cycloserine has been shown to exert anticonvulsant activity in maximal electroshock seizures. The purpose of the present study was to evaluate the spectrum of D-cycloserine anticonvulsant activity using other experimental models of epilepsy. D-Cycloserine induced a dose-related decrease in the incidence of tonic convulsions induced by 120 mg/kg of pentylenetetrazol. The ED50 of D-cycloserine for the inhibition of the tonic convulsions was 109 mg/kg. The anticonvulsant activity was specific for the D-isomer at L-cycloserine (400 mg/kg) had no effect on the tonic convulsions. D-Cycloserine had no effect on the pentylenetetrazol-induced clonic convulsions induced by either 70 or 120 mg/kg pentylenetetrazol, electrically induced nonkindled hippocampal seizures or kindled amygdala seizures. D-Cycloserine had no effect on strychnine-induced tonic convulsions. These results indicate that D-cycloserine is inactive against clonic convulsions and may be active only against tonic convulsions mediated by brainstem sites.
D-环丝氨酸已被证明在最大电休克惊厥中具有抗惊厥活性。本研究的目的是使用其他癫痫实验模型评估D-环丝氨酸抗惊厥活性的范围。D-环丝氨酸可使由120mg/kg戊四氮诱导的强直性惊厥发生率呈剂量相关下降。D-环丝氨酸抑制强直性惊厥的半数有效剂量(ED50)为109mg/kg。抗惊厥活性对D-异构体具有特异性,因为L-环丝氨酸(400mg/kg)对强直性惊厥没有影响。D-环丝氨酸对70mg/kg或120mg/kg戊四氮诱导的戊四氮性阵挛性惊厥、电诱导的非点燃海马惊厥或点燃杏仁核惊厥均无影响。D-环丝氨酸对士的宁诱导的强直性惊厥也没有影响。这些结果表明,D-环丝氨酸对阵挛性惊厥无活性,可能仅对脑干部位介导的强直性惊厥有活性。