{"title":"对精神分裂症皮质伽马振荡不足所隐含的突触变化的平均场分析","authors":"Deying Song, Daniel W Chung, G Bard Ermentrout","doi":"10.1007/s10827-024-00884-0","DOIUrl":null,"url":null,"abstract":"<p><p>Deficient gamma oscillations in the prefrontal cortex (PFC) of individuals with schizophrenia (SZ) are proposed to arise from alterations in the excitatory drive to fast-spiking interneurons (E <math><mo>→</mo></math> I) and in the inhibitory drive from these interneurons to excitatory neurons (I <math><mo>→</mo></math> E). Consistent with this idea, prior postmortem studies showed lower levels of molecular and structural markers for the strength of E <math><mo>→</mo></math> I and I <math><mo>→</mo></math> E synapses and also greater variability in E <math><mo>→</mo></math> I synaptic strength in PFC of SZ. Moreover, simulating these alterations in a network of quadratic integrate-and-fire (QIF) neurons revealed a synergistic effect of their interactions on reducing gamma power. In this study, we aimed to investigate the dynamical nature of this synergistic interaction at macroscopic level by deriving a mean-field description of the QIF model network that consists of all-to-all connected excitatory neurons and fast-spiking interneurons. Through a series of numerical simulations and bifurcation analyses, findings from our mean-field model showed that the macroscopic dynamics of gamma oscillations are synergistically disrupted by the interactions among lower strength of E <math><mo>→</mo></math> I and I <math><mo>→</mo></math> E synapses and greater variability in E <math><mo>→</mo></math> I synaptic strength. Furthermore, the two-dimensional bifurcation analyses showed that this synergistic interaction is primarily driven by the shift in Hopf bifurcation due to lower E <math><mo>→</mo></math> I synaptic strength. Together, these simulations predict the nature of dynamical mechanisms by which multiple synaptic alterations interact to robustly reduce PFC gamma power in SZ, and highlight the utility of mean-field model to study macroscopic neural dynamics and their alterations in the illness.</p>","PeriodicalId":54857,"journal":{"name":"Journal of Computational Neuroscience","volume":" ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mean-field analysis of synaptic alterations underlying deficient cortical gamma oscillations in schizophrenia.\",\"authors\":\"Deying Song, Daniel W Chung, G Bard Ermentrout\",\"doi\":\"10.1007/s10827-024-00884-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Deficient gamma oscillations in the prefrontal cortex (PFC) of individuals with schizophrenia (SZ) are proposed to arise from alterations in the excitatory drive to fast-spiking interneurons (E <math><mo>→</mo></math> I) and in the inhibitory drive from these interneurons to excitatory neurons (I <math><mo>→</mo></math> E). Consistent with this idea, prior postmortem studies showed lower levels of molecular and structural markers for the strength of E <math><mo>→</mo></math> I and I <math><mo>→</mo></math> E synapses and also greater variability in E <math><mo>→</mo></math> I synaptic strength in PFC of SZ. Moreover, simulating these alterations in a network of quadratic integrate-and-fire (QIF) neurons revealed a synergistic effect of their interactions on reducing gamma power. In this study, we aimed to investigate the dynamical nature of this synergistic interaction at macroscopic level by deriving a mean-field description of the QIF model network that consists of all-to-all connected excitatory neurons and fast-spiking interneurons. Through a series of numerical simulations and bifurcation analyses, findings from our mean-field model showed that the macroscopic dynamics of gamma oscillations are synergistically disrupted by the interactions among lower strength of E <math><mo>→</mo></math> I and I <math><mo>→</mo></math> E synapses and greater variability in E <math><mo>→</mo></math> I synaptic strength. Furthermore, the two-dimensional bifurcation analyses showed that this synergistic interaction is primarily driven by the shift in Hopf bifurcation due to lower E <math><mo>→</mo></math> I synaptic strength. Together, these simulations predict the nature of dynamical mechanisms by which multiple synaptic alterations interact to robustly reduce PFC gamma power in SZ, and highlight the utility of mean-field model to study macroscopic neural dynamics and their alterations in the illness.</p>\",\"PeriodicalId\":54857,\"journal\":{\"name\":\"Journal of Computational Neuroscience\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2024-11-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Computational Neuroscience\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10827-024-00884-0\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"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/s10827-024-00884-0","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MATHEMATICAL & COMPUTATIONAL BIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
精神分裂症(SZ)患者前额叶皮质(PFC)中伽马振荡的缺陷被认为是由于快速尖峰中间神经元(E → I)的兴奋驱动力和这些中间神经元对兴奋神经元(I → E)的抑制驱动力发生了改变。与这一观点一致的是,先前的尸检研究显示,在 SZ 的 PFC 中,E → I 和 I → E 突触强度的分子和结构标记水平较低,E → I 突触强度的变异性也较大。此外,在一个四元整合-发射(QIF)神经元网络中模拟这些变化,发现它们之间的相互作用对降低伽马功率有协同作用。在这项研究中,我们的目的是通过推导由全对全连接的兴奋神经元和快速尖峰中间神经元组成的 QIF 模型网络的均场描述,在宏观水平上研究这种协同作用的动态性质。通过一系列数值模拟和分叉分析,我们的均场模型发现,伽马振荡的宏观动力学会受到E→I和I→E突触强度较低和E→I突触强度变化较大之间相互作用的协同干扰。此外,二维分叉分析表明,这种协同作用主要是由 E → I 突触强度降低导致的霍普夫分叉移动驱动的。总之,这些模拟预测了多种突触改变相互作用以有力降低 SZ 中 PFC γ 功率的动力学机制的性质,并突出了均场模型在研究疾病中的宏观神经动力学及其改变方面的实用性。
Mean-field analysis of synaptic alterations underlying deficient cortical gamma oscillations in schizophrenia.
Deficient gamma oscillations in the prefrontal cortex (PFC) of individuals with schizophrenia (SZ) are proposed to arise from alterations in the excitatory drive to fast-spiking interneurons (E I) and in the inhibitory drive from these interneurons to excitatory neurons (I E). Consistent with this idea, prior postmortem studies showed lower levels of molecular and structural markers for the strength of E I and I E synapses and also greater variability in E I synaptic strength in PFC of SZ. Moreover, simulating these alterations in a network of quadratic integrate-and-fire (QIF) neurons revealed a synergistic effect of their interactions on reducing gamma power. In this study, we aimed to investigate the dynamical nature of this synergistic interaction at macroscopic level by deriving a mean-field description of the QIF model network that consists of all-to-all connected excitatory neurons and fast-spiking interneurons. Through a series of numerical simulations and bifurcation analyses, findings from our mean-field model showed that the macroscopic dynamics of gamma oscillations are synergistically disrupted by the interactions among lower strength of E I and I E synapses and greater variability in E I synaptic strength. Furthermore, the two-dimensional bifurcation analyses showed that this synergistic interaction is primarily driven by the shift in Hopf bifurcation due to lower E I synaptic strength. Together, these simulations predict the nature of dynamical mechanisms by which multiple synaptic alterations interact to robustly reduce PFC gamma power in SZ, and highlight the utility of mean-field model to study macroscopic neural dynamics and their alterations in the illness.
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.