Suppr超能文献

天冬氨酸酰基转移酶/吸引素双突变小鼠中的失神样发作和强直性发作

Absence-like and tonic seizures in aspartoacylase/attractin double-mutant mice.

作者信息

Gohma Hiroshi, Kuramoto Takashi, Matalon Reuben, Surendran Sankar, Tyring Stephen, Kitada Kazuhiro, Sasa Masashi, Serikawa Tadao

机构信息

Institute of Laboratory Animals, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

Exp Anim. 2007 Apr;56(2):161-5. doi: 10.1538/expanim.56.161.

Abstract

The Spontaneously Epileptic Rat (SER), a double-mutant for tremor and zitter mutations, shows spontaneous occurrences of absence-like and tonic seizures. Several lines of evidence suggest that the combined effect of Aspa and Atrn mutations is the most likely cause of the epileptic phenotype of the SER. To address this issue, we produced a new double-mutant mouse line carrying both homozygous Aspa-knockout and Atrn(mg-3J) mutant alleles. The Aspa/Atrn double-mutant mice exhibited absence-like and tonic seizures that were characterized by the appearance of 5-7 Hz spike-wave-like complexes and low voltage fast waves on EEGs. These results demonstrate directly that the simultaneous loss of the Aspa and Atrn gene functions causes epileptic seizures in the mouse and suggest that both Aspa and Atrn deficiencies might be responsible for epileptic seizures in the SER.

摘要

自发性癫痫大鼠(SER)是震颤和颤抖突变的双突变体,表现出失神样发作和强直发作的自发发生。多条证据表明,Aspa和Atrn突变的联合作用最有可能是SER癫痫表型的原因。为了解决这个问题,我们培育了一种新的双突变小鼠品系,它携带纯合的Aspa基因敲除和Atrn(mg-3J)突变等位基因。Aspa/Atrn双突变小鼠表现出失神样发作和强直发作,其特征是脑电图上出现5-7Hz的棘波样复合波和低电压快波。这些结果直接证明,Aspa和Atrn基因功能的同时丧失会导致小鼠癫痫发作,并表明Aspa和Atrn的缺陷都可能是SER癫痫发作的原因。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验