{"title":"具有相关噪声的θ神经元的稳态和对周期性刺激发射率的反应。","authors":"Jannik Franzen, Lukas Ramlow, Benjamin Lindner","doi":"10.1007/s10827-022-00836-6","DOIUrl":null,"url":null,"abstract":"<p><p>The stochastic activity of neurons is caused by various sources of correlated fluctuations and can be described in terms of simplified, yet biophysically grounded, integrate-and-fire models. One paradigmatic model is the quadratic integrate-and-fire model and its equivalent phase description by the theta neuron. Here we study the theta neuron model driven by a correlated Ornstein-Uhlenbeck noise and by periodic stimuli. We apply the matrix-continued-fraction method to the associated Fokker-Planck equation to develop an efficient numerical scheme to determine the stationary firing rate as well as the stimulus-induced modulation of the instantaneous firing rate. For the stationary case, we identify the conditions under which the firing rate decreases or increases by the effect of the colored noise and compare our results to existing analytical approximations for limit cases. For an additional periodic signal we demonstrate how the linear and nonlinear response terms can be computed and report resonant behavior for some of them. We extend the method to the case of two periodic signals, generally with incommensurable frequencies, and present a particular case for which a strong mixed response to both signals is observed, i.e. where the response to the sum of signals differs significantly from the sum of responses to the single signals. We provide Python code for our computational method: https://github.com/jannikfranzen/theta_neuron .</p>","PeriodicalId":54857,"journal":{"name":"Journal of Computational Neuroscience","volume":"51 1","pages":"107-128"},"PeriodicalIF":1.5000,"publicationDate":"2023-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9840600/pdf/","citationCount":"0","resultStr":"{\"title\":\"The steady state and response to a periodic stimulation of the firing rate for a theta neuron with correlated noise.\",\"authors\":\"Jannik Franzen, Lukas Ramlow, Benjamin Lindner\",\"doi\":\"10.1007/s10827-022-00836-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The stochastic activity of neurons is caused by various sources of correlated fluctuations and can be described in terms of simplified, yet biophysically grounded, integrate-and-fire models. One paradigmatic model is the quadratic integrate-and-fire model and its equivalent phase description by the theta neuron. Here we study the theta neuron model driven by a correlated Ornstein-Uhlenbeck noise and by periodic stimuli. We apply the matrix-continued-fraction method to the associated Fokker-Planck equation to develop an efficient numerical scheme to determine the stationary firing rate as well as the stimulus-induced modulation of the instantaneous firing rate. For the stationary case, we identify the conditions under which the firing rate decreases or increases by the effect of the colored noise and compare our results to existing analytical approximations for limit cases. For an additional periodic signal we demonstrate how the linear and nonlinear response terms can be computed and report resonant behavior for some of them. We extend the method to the case of two periodic signals, generally with incommensurable frequencies, and present a particular case for which a strong mixed response to both signals is observed, i.e. where the response to the sum of signals differs significantly from the sum of responses to the single signals. We provide Python code for our computational method: https://github.com/jannikfranzen/theta_neuron .</p>\",\"PeriodicalId\":54857,\"journal\":{\"name\":\"Journal of Computational Neuroscience\",\"volume\":\"51 1\",\"pages\":\"107-128\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2023-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9840600/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Computational Neuroscience\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10827-022-00836-6\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/10/22 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"MATHEMATICAL & COMPUTATIONAL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Computational Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10827-022-00836-6","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/10/22 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"MATHEMATICAL & COMPUTATIONAL BIOLOGY","Score":null,"Total":0}
The steady state and response to a periodic stimulation of the firing rate for a theta neuron with correlated noise.
The stochastic activity of neurons is caused by various sources of correlated fluctuations and can be described in terms of simplified, yet biophysically grounded, integrate-and-fire models. One paradigmatic model is the quadratic integrate-and-fire model and its equivalent phase description by the theta neuron. Here we study the theta neuron model driven by a correlated Ornstein-Uhlenbeck noise and by periodic stimuli. We apply the matrix-continued-fraction method to the associated Fokker-Planck equation to develop an efficient numerical scheme to determine the stationary firing rate as well as the stimulus-induced modulation of the instantaneous firing rate. For the stationary case, we identify the conditions under which the firing rate decreases or increases by the effect of the colored noise and compare our results to existing analytical approximations for limit cases. For an additional periodic signal we demonstrate how the linear and nonlinear response terms can be computed and report resonant behavior for some of them. We extend the method to the case of two periodic signals, generally with incommensurable frequencies, and present a particular case for which a strong mixed response to both signals is observed, i.e. where the response to the sum of signals differs significantly from the sum of responses to the single signals. We provide Python code for our computational method: https://github.com/jannikfranzen/theta_neuron .
期刊介绍:
The Journal of Computational Neuroscience provides a forum for papers that fit the interface between computational and experimental work in the neurosciences. The Journal of Computational Neuroscience publishes full length original papers, rapid communications and review articles describing theoretical and experimental work relevant to computations in the brain and nervous system. Papers that combine theoretical and experimental work are especially encouraged. Primarily theoretical papers should deal with issues of obvious relevance to biological nervous systems. Experimental papers should have implications for the computational function of the nervous system, and may report results using any of a variety of approaches including anatomy, electrophysiology, biophysics, imaging, and molecular biology. Papers investigating the physiological mechanisms underlying pathologies of the nervous system, or papers that report novel technologies of interest to researchers in computational neuroscience, including advances in neural data analysis methods yielding insights into the function of the nervous system, are also welcomed (in this case, methodological papers should include an application of the new method, exemplifying the insights that it yields).It is anticipated that all levels of analysis from cognitive to cellular will be represented in the Journal of Computational Neuroscience.