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蹒跚突变小鼠失神发作的抗惊厥敏感性

Anticonvulsant sensitivity of absence seizures in the tottering mutant mouse.

作者信息

Heller A H, Dichter M A, Sidman R L

出版信息

Epilepsia. 1983 Feb;24(1):25-34. doi: 10.1111/j.1528-1157.1983.tb04862.x.

Abstract

Homozygous tottering mice (tg, autosomal recessive) exhibit frequent spontaneous "absence" seizures accompanied by bilaterally synchronous spike-and-wave or polyspike electrocorticographic discharges. In adult tottering mice, the antiepileptic effects of a single dose of ethosuximide, diazepam, phenobarbital, or phenytoin were assessed using continuous electrocorticographic recording to monitor seizure incidence. The dose chosen for each drug was selected to correspond to an effective antiepileptic dose in standard murine models. Ethosuximide, 150 mg/kg, diazepam, 1.4 mg/kg, and phenobarbital, 25 mg/kg were effective against absence seizures. In contrast, phenytoin at 5, 10, 30, or 60 mg/kg produced no significant reduction in the incidence of absence seizures. These results suggest that absence seizures in the tottering mutant may represent a relatively specific pharmacological model for the identification of drugs effective for clinical absence epilepsy, and emphasize the potential value of this new model for the study of fundamental mechanisms of absence of epilepsy and the actions of antiepileptic drugs.

摘要

纯合子蹒跚小鼠(tg,常染色体隐性)表现出频繁的自发性“失神”发作,伴有双侧同步的棘波和慢波或多棘波皮层脑电图放电。在成年蹒跚小鼠中,使用连续皮层脑电图记录来监测癫痫发作发生率,评估单剂量乙琥胺、地西泮、苯巴比妥或苯妥英的抗癫痫作用。为每种药物选择的剂量对应于标准小鼠模型中的有效抗癫痫剂量。150毫克/千克的乙琥胺、1.4毫克/千克的地西泮和25毫克/千克的苯巴比妥对失神发作有效。相比之下,5、10、30或60毫克/千克的苯妥英对失神发作的发生率没有显著降低。这些结果表明,蹒跚突变体中的失神发作可能代表一种相对特异的药理学模型,用于鉴定对临床失神癫痫有效的药物,并强调了这种新模型在研究失神癫痫的基本机制和抗癫痫药物作用方面的潜在价值。

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