• 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

实验室啮齿动物自发性复发性癫痫的模型与检测。

Models and detection of spontaneous recurrent seizures in laboratory rodents.

机构信息

Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC 27599, USA.

Psychology & Neuroscience Program, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Zool Res. 2017 Jul 18;38(4):171-179. doi: 10.24272/j.issn.2095-8137.2017.042.

DOI:10.24272/j.issn.2095-8137.2017.042
PMID:28825447
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5571473/
Abstract

Epilepsy, characterized by spontaneous recurrent seizures (SRS), is a serious and common neurological disorder afflicting an estimated 1% of the population worldwide. Animal experiments, especially those utilizing small laboratory rodents, remain essential to understanding the fundamental mechanisms underlying epilepsy and to prevent, diagnose, and treat this disease. While much attention has been focused on epileptogenesis in animal models of epilepsy, there is little discussion on SRS, the hallmark of epilepsy. This is in part due to the technical difficulties of rigorous SRS detection. In this review, we comprehensively summarize both genetic and acquired models of SRS and discuss the methodology used to monitor and detect SRS in mice and rats.

摘要

癫痫,其特征为自发性反复发作性癫痫发作(SRS),是一种严重且常见的神经系统疾病,估计全球有 1%的人口受到影响。动物实验,特别是利用小型实验室啮齿动物的实验,对于理解癫痫的基本机制以及预防、诊断和治疗这种疾病仍然至关重要。虽然人们对癫痫动物模型中的癫痫发生过程给予了很多关注,但对 SRS 的讨论却很少,而 SRS 正是癫痫的标志。这在一定程度上是由于严格检测 SRS 的技术困难所致。在这篇综述中,我们全面总结了 SRS 的遗传和获得性模型,并讨论了用于监测和检测小鼠和大鼠 SRS 的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02f5/5571473/b2355af60717/ZoolRes-38-4-171-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02f5/5571473/b2355af60717/ZoolRes-38-4-171-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02f5/5571473/b2355af60717/ZoolRes-38-4-171-g1.jpg

相似文献

1
Models and detection of spontaneous recurrent seizures in laboratory rodents.实验室啮齿动物自发性复发性癫痫的模型与检测。
Zool Res. 2017 Jul 18;38(4):171-179. doi: 10.24272/j.issn.2095-8137.2017.042.
2
Epilepsy induced by extended amygdala-kindling in rats: lack of clear association between development of spontaneous seizures and neuronal damage.大鼠杏仁核扩展点燃诱导的癫痫:自发性癫痫发作的发展与神经元损伤之间缺乏明确关联。
Epilepsy Res. 2004 Dec;62(2-3):135-56. doi: 10.1016/j.eplepsyres.2004.08.008.
3
Spontaneous recurrent seizures and neuropathology in the chronic phase of the pilocarpine and picrotoxin model epilepsy.匹鲁卡品和印防己毒素模型癫痫慢性期的自发性反复癫痫发作及神经病理学
Neurol Res. 2002 Mar;24(2):199-209. doi: 10.1179/016164102101199611.
4
The time course of acquired epilepsy: implications for therapeutic intervention to suppress epileptogenesis.获得性癫痫的时间进程:对抑制癫痫发生的治疗干预的影响。
Neurosci Lett. 2011 Jun 27;497(3):240-6. doi: 10.1016/j.neulet.2011.03.071. Epub 2011 Mar 31.
5
microRNA and Epilepsy.微小RNA与癫痫
Adv Exp Med Biol. 2015;888:41-70. doi: 10.1007/978-3-319-22671-2_4.
6
Toll-like receptor 3 deficiency decreases epileptogenesis in a pilocarpine model of SE-induced epilepsy in mice.Toll样受体3缺陷可降低毛果芸香碱诱导的小鼠癫痫持续状态模型中的癫痫发生。
Epilepsia. 2017 Apr;58(4):586-596. doi: 10.1111/epi.13688. Epub 2017 Feb 6.
7
Cortical hyperexcitability and epileptogenesis: Understanding the mechanisms of epilepsy - part 2.皮质兴奋性过高与癫痫发生:理解癫痫机制 - 第2部分
J Clin Neurosci. 2009 Apr;16(4):485-500. doi: 10.1016/j.jocn.2008.10.001. Epub 2009 Feb 20.
8
Genetic animal models of epilepsy as a unique resource for the evaluation of anticonvulsant drugs. A review.癫痫的遗传动物模型作为评估抗惊厥药物的独特资源。综述。
Methods Find Exp Clin Pharmacol. 1984 Sep;6(9):531-47.
9
Animal models.动物模型。
Handb Clin Neurol. 2012;107:63-98. doi: 10.1016/B978-0-444-52898-8.00004-5.
10
Molecular tools for the characterization of seizure susceptibility in genetic rodent models of epilepsy.用于遗传癫痫啮齿动物模型中癫痫易感性特征分析的分子工具。
Epilepsy Behav. 2021 Aug;121(Pt B):106594. doi: 10.1016/j.yebeh.2019.106594. Epub 2019 Nov 1.

引用本文的文献

1
Development of a preclinical testing platform for clinically relevant therapy for Dravet syndrome.开发用于Dravet综合征临床相关治疗的临床前测试平台。
Epilepsia. 2025 Jun 30. doi: 10.1111/epi.18516.
2
Neurodevelopmental defects in a mouse model of O-GlcNAc transferase intellectual disability.O-连接的N-乙酰葡糖胺转移酶智力障碍小鼠模型中的神经发育缺陷
Dis Model Mech. 2024 Apr 1;17(4). doi: 10.1242/dmm.050671. Epub 2024 Apr 25.
3
Animal Models of Drug-Resistant Epilepsy as Tools for Deciphering the Cellular and Molecular Mechanisms of Pharmacoresistance and Discovering More Effective Treatments.

本文引用的文献

1
Upholding WAG/Rij rats as a model of absence epileptogenesis: Hidden mechanisms and a new theory on seizure development.维持 WAG/Rij 大鼠作为失神癫痫发生模型:潜在机制和发作发展的新理论。
Neurosci Biobehav Rev. 2016 Dec;71:388-408. doi: 10.1016/j.neubiorev.2016.09.017. Epub 2016 Sep 26.
2
Eight Flurothyl-Induced Generalized Seizures Lead to the Rapid Evolution of Spontaneous Seizures in Mice: A Model of Epileptogenesis with Seizure Remission.八氟乙烷诱发的全身性癫痫发作导致小鼠自发性癫痫发作的快速演变:一种伴有癫痫发作缓解的癫痫发生模型。
J Neurosci. 2016 Jul 13;36(28):7485-96. doi: 10.1523/JNEUROSCI.3232-14.2016.
3
耐药性癫痫的动物模型作为破译药物抵抗的细胞和分子机制以及发现更有效的治疗方法的工具。
Cells. 2023 Apr 24;12(9):1233. doi: 10.3390/cells12091233.
4
Scoping review of disease-modifying effect of drugs in experimental epilepsy.药物对实验性癫痫疾病修饰作用的范围综述
Front Neurol. 2023 Feb 23;14:1097473. doi: 10.3389/fneur.2023.1097473. eCollection 2023.
5
Sustained overexpression of spliced X-box-binding protein-1 in neurons leads to spontaneous seizures and sudden death in mice.神经元中剪接 X 盒结合蛋白-1 的持续过表达可导致小鼠自发性癫痫发作和突然死亡。
Commun Biol. 2023 Mar 9;6(1):252. doi: 10.1038/s42003-023-04594-8.
6
The role of network connectivity on epileptiform activity.网络连通性对癫痫样活动的作用。
Sci Rep. 2021 Oct 21;11(1):20792. doi: 10.1038/s41598-021-00283-w.
7
Characterization and treatment of spontaneous recurrent seizures following nerve agent-induced status epilepticus in mice.在诱导癫痫持续状态后自发反复性癫痫发作的特征及治疗:小鼠模型。
Epilepsy Res. 2020 May;162:106320. doi: 10.1016/j.eplepsyres.2020.106320. Epub 2020 Mar 10.
8
Potential Role of miRNAs as Theranostic Biomarkers of Epilepsy.微小RNA作为癫痫诊疗生物标志物的潜在作用
Mol Ther Nucleic Acids. 2018 Dec 7;13:275-290. doi: 10.1016/j.omtn.2018.09.008. Epub 2018 Sep 13.
GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility.
泛素蛋白连接酶E3A在γ-氨基丁酸能神经元中的特异性缺失导致类似天使综合征的脑电图异常并增强癫痫易感性。
Neuron. 2016 Apr 6;90(1):56-69. doi: 10.1016/j.neuron.2016.02.040. Epub 2016 Mar 24.
4
Genetically epilepsy-prone rats (GEPRs) and DBA/2 mice: Two animal models of audiogenic reflex epilepsy for the evaluation of new generation AEDs.遗传性癫痫易感大鼠(GEPRs)和DBA/2小鼠:两种用于评估新一代抗癫痫药物的听源性反射癫痫动物模型。
Epilepsy Behav. 2017 Jun;71(Pt B):165-173. doi: 10.1016/j.yebeh.2015.06.030. Epub 2015 Aug 6.
5
Disruption of Fgf13 causes synaptic excitatory-inhibitory imbalance and genetic epilepsy and febrile seizures plus.Fgf13的破坏会导致突触兴奋性-抑制性失衡、遗传性癫痫和热性惊厥附加症。
J Neurosci. 2015 Jun 10;35(23):8866-81. doi: 10.1523/JNEUROSCI.3470-14.2015.
6
Glutamatergic neuron-targeted loss of LGI1 epilepsy gene results in seizures.LGI1癫痫基因在谷氨酸能神经元中的靶向缺失会导致癫痫发作。
Brain. 2014 Nov;137(Pt 11):2984-96. doi: 10.1093/brain/awu259. Epub 2014 Sep 17.
7
Convulsive seizures and SUDEP in a mouse model of SCN8A epileptic encephalopathy.SCN8A 癫痫性脑病小鼠模型中的惊厥性癫痫发作和癫痫性猝死
Hum Mol Genet. 2015 Jan 15;24(2):506-15. doi: 10.1093/hmg/ddu470. Epub 2014 Sep 16.
8
Candidate drug targets for prevention or modification of epilepsy.用于预防或改善癫痫的候选药物靶点。
Annu Rev Pharmacol Toxicol. 2015;55:229-47. doi: 10.1146/annurev-pharmtox-010814-124607. Epub 2014 Aug 25.
9
The consequences of refractory epilepsy and its treatment.难治性癫痫的后果及其治疗。
Epilepsy Behav. 2014 Aug;37:59-70. doi: 10.1016/j.yebeh.2014.05.031. Epub 2014 Jun 27.
10
The role of T-type calcium channel genes in absence seizures.T型钙通道基因在失神发作中的作用。
Front Neurol. 2014 May 9;5:45. doi: 10.3389/fneur.2014.00045. eCollection 2014.