• 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

相似文献

1
Are the Breaks Breaking Down?这些骨折正在恶化吗?
Epilepsy Curr. 2019 Mar-Apr;19(2):117-118. doi: 10.1177/1535759719835350.
2
Altered hippocampal interneuron activity precedes ictal onset.海马区中间神经元活动的改变先于癫痫发作的开始。
Elife. 2018 Nov 2;7:e40750. doi: 10.7554/eLife.40750.
3
Feedforward inhibition ahead of ictal wavefronts is provided by both parvalbumin- and somatostatin-expressing interneurons.在痫性波阵面之前,由表达 parvalbumin 和 somatostatin 的中间神经元提供前馈抑制。
J Physiol. 2019 Apr;597(8):2297-2314. doi: 10.1113/JP277749. Epub 2019 Mar 18.
4
Selective activation of parvalbumin- or somatostatin-expressing interneurons triggers epileptic seizurelike activity in mouse medial entorhinal cortex.选择性激活表达小白蛋白或生长抑素的中间神经元会在小鼠内侧内嗅皮层引发癫痫样发作活动。
J Neurophysiol. 2015 Mar 1;113(5):1616-30. doi: 10.1152/jn.00841.2014. Epub 2014 Dec 10.
5
Inhibition by Somatostatin Interneurons in Olfactory Cortex.嗅觉皮层中生长抑素中间神经元的抑制作用
Front Neural Circuits. 2016 Aug 17;10:62. doi: 10.3389/fncir.2016.00062. eCollection 2016.
6
Excitatory Inputs Determine Phase-Locking Strength and Spike-Timing of CA1 Stratum Oriens/Alveus Parvalbumin and Somatostatin Interneurons during Intrinsically Generated Hippocampal Theta Rhythm.兴奋性输入决定海马内源性θ节律期间CA1海马伞/海马槽小白蛋白和生长抑素中间神经元的锁相强度和峰电位时间。
J Neurosci. 2016 Jun 22;36(25):6605-22. doi: 10.1523/JNEUROSCI.3951-13.2016.
7
Unit Activity of Hippocampal Interneurons before Spontaneous Seizures in an Animal Model of Temporal Lobe Epilepsy.颞叶癫痫动物模型中自发癫痫发作前海马中间神经元的单位活动
J Neurosci. 2015 Apr 22;35(16):6600-18. doi: 10.1523/JNEUROSCI.4786-14.2015.
8
Chemogenetic Recruitment of Specific Interneurons Suppresses Seizure Activity.特定中间神经元的化学遗传募集可抑制癫痫活动。
Front Cell Neurosci. 2018 Sep 5;12:293. doi: 10.3389/fncel.2018.00293. eCollection 2018.
9
The antiepileptic and ictogenic effects of optogenetic neurostimulation of PV-expressing interneurons.对表达小白蛋白的中间神经元进行光遗传学神经刺激的抗癫痫和致痫作用。
J Neurophysiol. 2016 Oct 1;116(4):1694-1704. doi: 10.1152/jn.00744.2015. Epub 2016 Jul 13.
10
Neuronal synchrony and the transition to spontaneous seizures.神经元同步与自发性癫痫发作的转变。
Exp Neurol. 2013 Oct;248:72-84. doi: 10.1016/j.expneurol.2013.05.004. Epub 2013 May 23.

本文引用的文献

1
Brain State Is a Major Factor in Preseizure Hippocampal Network Activity and Influences Success of Seizure Intervention.脑状态是癫痫发作前海马体网络活动的主要因素,并影响癫痫发作干预的成功率。
J Neurosci. 2015 Nov 25;35(47):15635-48. doi: 10.1523/JNEUROSCI.5112-14.2015.
2
The role of inhibition in epileptic networks.抑制在癫痫网络中的作用。
J Clin Neurophysiol. 2015 Jun;32(3):227-34. doi: 10.1097/WNP.0000000000000160.
3
Unit Activity of Hippocampal Interneurons before Spontaneous Seizures in an Animal Model of Temporal Lobe Epilepsy.颞叶癫痫动物模型中自发癫痫发作前海马中间神经元的单位活动
J Neurosci. 2015 Apr 22;35(16):6600-18. doi: 10.1523/JNEUROSCI.4786-14.2015.
4
A reorganized GABAergic circuit in a model of epilepsy: evidence from optogenetic labeling and stimulation of somatostatin interneurons.癫痫模型中的 GABA 能回路重组:来自光遗传标记和生长抑素中间神经元刺激的证据。
J Neurosci. 2013 Sep 4;33(36):14392-405. doi: 10.1523/JNEUROSCI.2045-13.2013.
5
Early activation of ventral hippocampus and subiculum during spontaneous seizures in a rat model of temporal lobe epilepsy.颞叶癫痫大鼠模型自发发作期间腹侧海马和下托的早期激活。
J Neurosci. 2013 Jul 3;33(27):11100-15. doi: 10.1523/JNEUROSCI.0472-13.2013.
6
Neuronal synchrony and the transition to spontaneous seizures.神经元同步与自发性癫痫发作的转变。
Exp Neurol. 2013 Oct;248:72-84. doi: 10.1016/j.expneurol.2013.05.004. Epub 2013 May 23.
7
On-demand optogenetic control of spontaneous seizures in temporal lobe epilepsy.按需光遗传学控制颞叶癫痫的自发性癫痫发作。
Nat Commun. 2013;4:1376. doi: 10.1038/ncomms2376.
8
Feedforward inhibition contributes to the control of epileptiform propagation speed.前馈抑制有助于控制癫痫样放电的传播速度。
J Neurosci. 2007 Mar 28;27(13):3383-7. doi: 10.1523/JNEUROSCI.0145-07.2007.

这些骨折正在恶化吗?

Are the Breaks Breaking Down?

作者信息

Ewell Laura A

出版信息

Epilepsy Curr. 2019 Mar-Apr;19(2):117-118. doi: 10.1177/1535759719835350.

DOI:10.1177/1535759719835350
PMID:30955417
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6610410/
Abstract

Altered Hippocampal Interneuron Activity Precedes Ictal Onset Miri ML, Vinck M, Pant R, Cardin JA. Elife. 2018;7. pii: e40750. doi:10.7554/eLife.40750. Although failure of GABAergic inhibition is a commonly hypothesized mechanism underlying seizure disorders, the series of events that precipitates a rapid shift from healthy to ictal activity remains unclear. Furthermore, the diversity of inhibitory interneuron populations poses a challenge for understanding local circuit interactions during seizure initiation. Using a combined optogenetic and electrophysiological approach, we examined the activity of identified mouse hippocampal interneuron classes during chemoconvulsant seizure induction in vivo. Surprisingly, synaptic inhibition from parvalbumin-(PV) and somatostatin-expressing (SST) interneurons remained intact throughout the preictal period and early ictal phase. However, these 2 sources of inhibition exhibited cell type-specific differences in their preictal firing patterns and sensitivity to input. Our findings suggest that the onset of ictal activity is not associated with loss of firing by these interneurons or a failure of synaptic inhibition but is instead linked with disruptions of the respective roles these interneurons play in the hippocampal circuit.

摘要

海马体中间神经元活动改变先于癫痫发作起始

米里·ML、温克·M、潘特·R、卡丁·JA。《eLife》。2018年;7。文章编号:e40750。doi:10.7554/eLife.40750。尽管γ-氨基丁酸能抑制功能失效是癫痫疾病常见的潜在发病机制,但导致从健康状态迅速转变为癫痫发作活动的一系列事件仍不清楚。此外,抑制性中间神经元群体的多样性对理解癫痫发作起始时的局部回路相互作用构成了挑战。我们采用光遗传学和电生理学相结合的方法,在体内化学惊厥诱导过程中研究了已鉴定的小鼠海马体中间神经元类别的活动。令人惊讶的是,在发作前期和癫痫发作早期,小白蛋白(PV)和生长抑素表达(SST)中间神经元的突触抑制作用始终保持完整。然而,这两种抑制来源在发作前期放电模式和对输入的敏感性方面表现出细胞类型特异性差异。我们的研究结果表明,癫痫发作活动的起始并非与这些中间神经元的放电丧失或突触抑制功能失效相关,而是与这些中间神经元在海马体回路中所起的各自作用受到破坏有关。