Gohma Hiroshi, Kuramoto Takashi, Matalon Reuben, Surendran Sankar, Tyring Stephen, Kitada Kazuhiro, Sasa Masashi, Serikawa Tadao
Institute of Laboratory Animals, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Exp Anim. 2007 Apr;56(2):161-5. doi: 10.1538/expanim.56.161.
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.
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。