• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

Fyn激酶缺陷小鼠对听源性惊厥的易感性增强。

Enhanced susceptibility of audiogenic seizures in Fyn-kinase deficient mice.

作者信息

Miyakawa T, Yagi T, Taniguchi M, Matsuura H, Tateishi K, Niki H

机构信息

Department of Psychology, Faculty of Letters, University of Tokyo, Japan.

出版信息

Brain Res Mol Brain Res. 1995 Feb;28(2):349-52. doi: 10.1016/0169-328x(94)00251-9.

DOI:10.1016/0169-328x(94)00251-9
PMID:7723633
Abstract

Mice with a mutation in fyn genes were examined for their susceptibility to acoustically primed audiogenic seizures. Homozygous mutant (fynz/fynz) mice were significantly more likely to have seizures and to show the stronger seizure syndrome (clonus). These results indicate that the susceptibility of acoustically primed audiogenic seizures is enhanced in the Fyn kinase deficient mice.

摘要

对fyn基因发生突变的小鼠进行了声学引发的听源性癫痫易感性检测。纯合突变体(fynz/fynz)小鼠发生癫痫和表现出更强癫痫综合征(阵挛)的可能性显著更高。这些结果表明,Fyn激酶缺陷型小鼠对声学引发的听源性癫痫的易感性增强。

相似文献

1
Enhanced susceptibility of audiogenic seizures in Fyn-kinase deficient mice.Fyn激酶缺陷小鼠对听源性惊厥的易感性增强。
Brain Res Mol Brain Res. 1995 Feb;28(2):349-52. doi: 10.1016/0169-328x(94)00251-9.
2
Radial maze performance, open-field and elevated plus-maze behaviors in Fyn-kinase deficient mice: further evidence for increased fearfulness.Fyn激酶缺陷小鼠的放射状迷宫表现、旷场和高架十字迷宫行为:恐惧增加的进一步证据。
Brain Res Mol Brain Res. 1996 Apr;37(1-2):145-50. doi: 10.1016/0169-328x(95)00300-h.
3
Reduced susceptibility to seizures in carbonic anhydrase II deficient mutant mice.
Epilepsy Res. 1993 Feb;14(2):115-21. doi: 10.1016/0920-1211(93)90016-z.
4
Susceptibility to drug-induced seizures of Fyn tyrosine kinase-deficient mice.
Neuroreport. 1996 Nov 4;7(15-17):2723-6. doi: 10.1097/00001756-199611040-00063.
5
Periaqueductal gray neurons exhibit increased responsiveness associated with audiogenic seizures in the genetically epilepsy-prone rat.在遗传性癫痫易感大鼠中,导水管周围灰质神经元表现出与听源性癫痫发作相关的反应性增加。
Neuroscience. 1998 May;84(2):619-25. doi: 10.1016/s0306-4522(97)00551-4.
6
Increased fearfulness of Fyn tyrosine kinase deficient mice.Fyn酪氨酸激酶缺陷小鼠的恐惧加剧。
Brain Res Mol Brain Res. 1994 Nov;27(1):179-82. doi: 10.1016/0169-328x(94)90201-1.
7
Effect of precollicular transection on audiogenic seizures in genetically epilepsy-prone rats.中脑前丘横断对遗传性癫痫易感性大鼠听源性惊厥的影响。
Exp Neurol. 1999 Feb;155(2):295-301. doi: 10.1006/exnr.1998.6981.
8
Deficiency of Vlgr1 resulted in deafness and susceptibility to audiogenic seizures while the degree of hearing impairment was not correlated with seizure severity in C57BL/6- and 129-backcrossed lines of Vlgr1 knockout mice.在C57BL/6和129回交的Vlgr1基因敲除小鼠品系中,Vlgr1基因缺失导致耳聋和对听源性惊厥敏感,而听力损伤程度与惊厥严重程度无关。
Neurosci Lett. 2009 Sep 18;461(2):190-5. doi: 10.1016/j.neulet.2009.06.012. Epub 2009 Jun 17.
9
Brainstem seizure severity regulates forebrain seizure expression in the audiogenic kindling model.在听源性点燃模型中,脑干癫痫发作严重程度调节前脑癫痫发作表现。
Epilepsia. 2005 Sep;46(9):1380-8. doi: 10.1111/j.1528-1167.2005.39404.x.
10
An Scn1a epilepsy mutation in Scn8a alters seizure susceptibility and behavior.Scn8a 中的 Scn1a 癫痫突变会改变癫痫易感性和行为。
Exp Neurol. 2016 Jan;275 Pt 1(0 1):46-58. doi: 10.1016/j.expneurol.2015.09.008. Epub 2015 Sep 26.

引用本文的文献

1
Fyn-tau Ablation Modifies PTZ-Induced Seizures and Post-seizure Hallmarks of Early Epileptogenesis.Fyn-τ基因敲除改变戊四氮诱导的癫痫发作及早期癫痫发生的发作后特征。
Front Cell Neurosci. 2020 Dec 8;14:592374. doi: 10.3389/fncel.2020.592374. eCollection 2020.
2
fosB-null mice display impaired adult hippocampal neurogenesis and spontaneous epilepsy with depressive behavior.fosB 缺失型小鼠表现出成年海马神经发生受损和自发性癫痫伴抑郁行为。
Neuropsychopharmacology. 2013 Apr;38(5):895-906. doi: 10.1038/npp.2012.260. Epub 2012 Dec 18.
3
Regulation of Na(v)1.2 channels by brain-derived neurotrophic factor, TrkB, and associated Fyn kinase.
脑源性神经营养因子、酪氨酸激酶受体B(TrkB)及相关的Fyn激酶对电压门控性钠通道1.2(Na(v)1.2)的调节
J Neurosci. 2007 Oct 24;27(43):11533-42. doi: 10.1523/JNEUROSCI.5005-06.2007.
4
Growth factor-mediated Fyn signaling regulates alpha-amino-3- hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor expression in rodent neocortical neurons.生长因子介导的Fyn信号传导调节啮齿动物新皮质神经元中α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体的表达。
Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2461-6. doi: 10.1073/pnas.96.5.2461.
5
Rescuing impairment of long-term potentiation in fyn-deficient mice by introducing Fyn transgene.通过引入Fyn转基因挽救fyn基因缺陷小鼠的长时程增强损伤。
Proc Natl Acad Sci U S A. 1997 Apr 29;94(9):4761-5. doi: 10.1073/pnas.94.9.4761.