• 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

神经元生物物理网络中多种节律的相互作用。

Interactions of multiple rhythms in a biophysical network of neurons.

作者信息

Gelastopoulos Alexandros, Kopell Nancy J

机构信息

Department of Mathematics and Statistics, Boston University, 111 Cummington Mall, 02215, Boston, MA, USA.

Department of Marketing and Management, University of Southern Denmark, Campusvej 55, 5230, Odense, Denmark.

出版信息

J Math Neurosci. 2020 Nov 17;10(1):19. doi: 10.1186/s13408-020-00096-7.

DOI:10.1186/s13408-020-00096-7
PMID:33201339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7671958/
Abstract

Neural oscillations, including rhythms in the beta1 band (12-20 Hz), are important in various cognitive functions. Often neural networks receive rhythmic input at frequencies different from their natural frequency, but very little is known about how such input affects the network's behavior. We use a simplified, yet biophysical, model of a beta1 rhythm that occurs in the parietal cortex, in order to study its response to oscillatory inputs. We demonstrate that a cell has the ability to respond at the same time to two periodic stimuli of unrelated frequencies, firing in phase with one, but with a mean firing rate equal to that of the other. We show that this is a very general phenomenon, independent of the model used. We next show numerically that the behavior of a different cell, which is modeled as a high-dimensional dynamical system, can be described in a surprisingly simple way, owing to a reset that occurs in the state space when the cell fires. The interaction of the two cells leads to novel combinations of properties for neural dynamics, such as mode-locking to an input without phase-locking to it.

摘要

神经振荡,包括β1频段(12 - 20赫兹)的节律,在各种认知功能中都很重要。神经网络常常会接收到频率与其固有频率不同的节律性输入,但对于这种输入如何影响网络行为却知之甚少。我们使用一种简化但具有生物物理性质的顶叶皮层β1节律模型,来研究其对振荡输入的响应。我们证明,一个细胞能够同时对两个频率不相关的周期性刺激做出反应,与其中一个刺激同相放电,但其平均放电率与另一个刺激相同。我们表明这是一个非常普遍的现象,与所使用的模型无关。接下来我们通过数值模拟表明,另一个被建模为高维动力系统的细胞的行为,可以用一种惊人的简单方式来描述,这是由于细胞放电时状态空间中发生的重置。这两个细胞的相互作用导致了神经动力学特性的新组合,比如锁定到一个输入但不与之锁相。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/ddbc0627857a/13408_2020_96_Fig25_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/fcd1536f1f37/13408_2020_96_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/69df5e9e1c10/13408_2020_96_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/2c7df9350259/13408_2020_96_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/94b653f08044/13408_2020_96_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/a304a54f9fe6/13408_2020_96_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/fa53ee58f9e8/13408_2020_96_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/844593c4b444/13408_2020_96_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/cb934dab7366/13408_2020_96_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/940e7c5c1f8c/13408_2020_96_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/09e6baec59de/13408_2020_96_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/58104ed1d6d2/13408_2020_96_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/483c8fe47825/13408_2020_96_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/4be7080ecd5a/13408_2020_96_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/29360ce3a7df/13408_2020_96_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/f95cbec8bd67/13408_2020_96_Fig15_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/58bce33ee148/13408_2020_96_Fig16_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/4c503b78e97f/13408_2020_96_Fig17_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/64e5053de6df/13408_2020_96_Fig18_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/3ecab4f6c4ac/13408_2020_96_Fig19_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/c2b53ec57f95/13408_2020_96_Fig20_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/3f459d48bbed/13408_2020_96_Fig21_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/53ba8a3d7468/13408_2020_96_Fig22_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/9a8be8a00c72/13408_2020_96_Fig23_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/b742ced2d853/13408_2020_96_Fig24_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/ddbc0627857a/13408_2020_96_Fig25_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/fcd1536f1f37/13408_2020_96_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/69df5e9e1c10/13408_2020_96_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/2c7df9350259/13408_2020_96_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/94b653f08044/13408_2020_96_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/a304a54f9fe6/13408_2020_96_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/fa53ee58f9e8/13408_2020_96_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/844593c4b444/13408_2020_96_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/cb934dab7366/13408_2020_96_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/940e7c5c1f8c/13408_2020_96_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/09e6baec59de/13408_2020_96_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/58104ed1d6d2/13408_2020_96_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/483c8fe47825/13408_2020_96_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/4be7080ecd5a/13408_2020_96_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/29360ce3a7df/13408_2020_96_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/f95cbec8bd67/13408_2020_96_Fig15_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/58bce33ee148/13408_2020_96_Fig16_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/4c503b78e97f/13408_2020_96_Fig17_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/64e5053de6df/13408_2020_96_Fig18_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/3ecab4f6c4ac/13408_2020_96_Fig19_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/c2b53ec57f95/13408_2020_96_Fig20_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/3f459d48bbed/13408_2020_96_Fig21_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/53ba8a3d7468/13408_2020_96_Fig22_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/9a8be8a00c72/13408_2020_96_Fig23_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/b742ced2d853/13408_2020_96_Fig24_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f20d/7671958/ddbc0627857a/13408_2020_96_Fig25_HTML.jpg

相似文献

1
Interactions of multiple rhythms in a biophysical network of neurons.神经元生物物理网络中多种节律的相互作用。
J Math Neurosci. 2020 Nov 17;10(1):19. doi: 10.1186/s13408-020-00096-7.
2
Shaping Intrinsic Neural Oscillations with Periodic Stimulation.通过周期性刺激塑造内在神经振荡
J Neurosci. 2016 May 11;36(19):5328-37. doi: 10.1523/JNEUROSCI.0236-16.2016.
3
Orientation tuning properties of simple cells in area V1 derived from an approximate analysis of nonlinear neural field models.基于非线性神经场模型的近似分析得出的V1区简单细胞的方向调谐特性。
Neural Comput. 2001 Aug;13(8):1721-47. doi: 10.1162/08997660152469323.
4
Spiking resonances in models with the same slow resonant and fast amplifying currents but different subthreshold dynamic properties.具有相同缓慢共振电流和快速放大电流但不同阈下动态特性的模型中的峰值共振。
J Comput Neurosci. 2017 Dec;43(3):243-271. doi: 10.1007/s10827-017-0661-9. Epub 2017 Oct 24.
5
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.
6
Analyzing the competition of gamma rhythms with delayed pulse-coupled oscillators in phase representation.分析相位表示中的延迟脉冲耦合振荡器的伽马节律竞争。
Phys Rev E. 2018 Aug;98(2-1):022217. doi: 10.1103/PhysRevE.98.022217.
7
Multi-band oscillations emerge from a simple spiking network.多频段振荡源自一个简单的尖峰网络。
Chaos. 2023 Apr 1;33(4). doi: 10.1063/5.0106884.
8
Macroscopic phase resetting-curves determine oscillatory coherence and signal transfer in inter-coupled neural circuits.宏观相位重设曲线决定了耦合神经网络回路中的振荡相干性和信号传递。
PLoS Comput Biol. 2019 May 9;15(5):e1007019. doi: 10.1371/journal.pcbi.1007019. eCollection 2019 May.
9
A stochastic model of input effectiveness during irregular gamma rhythms.不规则伽马节律期间输入有效性的随机模型。
J Comput Neurosci. 2016 Feb;40(1):85-101. doi: 10.1007/s10827-015-0583-3. Epub 2015 Nov 26.
10
Synaptic origin and stimulus dependency of neuronal oscillatory activity in the primary visual cortex of the cat.猫初级视觉皮层中神经元振荡活动的突触起源和刺激依赖性
J Physiol. 1997 May 1;500 ( Pt 3)(Pt 3):751-74. doi: 10.1113/jphysiol.1997.sp022056.

引用本文的文献

1
Noninvasive inference methods for interaction and noise intensities of coupled oscillators using only spike time data.仅使用尖峰时间数据对耦合振荡器的相互作用和噪声强度进行非侵入式推断的方法。
Proc Natl Acad Sci U S A. 2022 Feb 8;119(6). doi: 10.1073/pnas.2113620119.

本文引用的文献

1
Parietal low beta rhythm provides a dynamical substrate for a working memory buffer.顶叶低频β节律为工作记忆缓冲提供了动力基础。
Proc Natl Acad Sci U S A. 2019 Aug 13;116(33):16613-16620. doi: 10.1073/pnas.1902305116. Epub 2019 Aug 1.
2
When brain rhythms aren't 'rhythmic': implication for their mechanisms and meaning.当脑节律“无节律”时:对其机制及意义的启示
Curr Opin Neurobiol. 2016 Oct;40:72-80. doi: 10.1016/j.conb.2016.06.010. Epub 2016 Jul 9.
3
Rhythms for Cognition: Communication through Coherence.认知的节奏:通过连贯性进行交流。
Neuron. 2015 Oct 7;88(1):220-35. doi: 10.1016/j.neuron.2015.09.034.
4
What does gamma coherence tell us about inter-regional neural communication?γ 相干性能告诉我们关于区域间神经通信的哪些信息?
Nat Neurosci. 2015 Apr;18(4):484-9. doi: 10.1038/nn.3952. Epub 2015 Feb 23.
5
Beyond the connectome: the dynome.超越连接组:动态组。
Neuron. 2014 Sep 17;83(6):1319-28. doi: 10.1016/j.neuron.2014.08.016.
6
Interareal oscillatory synchronization in top-down neocortical processing.自上而下的新皮层处理中的区域间振荡同步
Curr Opin Neurobiol. 2015 Apr;31:62-6. doi: 10.1016/j.conb.2014.08.010. Epub 2014 Sep 15.
7
The psychophysics of brain rhythms.脑节律的心理物理学。
Front Psychol. 2011 Aug 27;2:203. doi: 10.3389/fpsyg.2011.00203. eCollection 2011.
8
Control of multistability in ring circuits of oscillators.振荡器环形电路中多稳定性的控制。
Biol Cybern. 1999 Feb;80(2):87-102. doi: 10.1007/s004220050507.
9
Oscillations in the prefrontal cortex: a gateway to memory and attention.前额皮质的波动:通向记忆和注意力的大门。
Curr Opin Neurobiol. 2011 Jun;21(3):475-85. doi: 10.1016/j.conb.2011.01.004. Epub 2011 Mar 21.
10
Neural synchrony in cortical networks: history, concept and current status.皮质网络中的神经同步:历史、概念和现状。
Front Integr Neurosci. 2009 Jul 30;3:17. doi: 10.3389/neuro.07.017.2009. eCollection 2009.