刺激报告过程中小鼠大脑皮层反馈动态的神经和计算结构。

IF 2.7 3区 医学 Q3 NEUROSCIENCES eNeuro Pub Date : 2024-09-25 Print Date: 2024-09-01 DOI:10.1523/ENEURO.0191-24.2024
Simone Ciceri, Matthijs N Oude Lohuis, Vivi Rottschäfer, Cyriel M A Pennartz, Daniele Avitabile, Simon van Gaal, Umberto Olcese
{"title":"刺激报告过程中小鼠大脑皮层反馈动态的神经和计算结构。","authors":"Simone Ciceri, Matthijs N Oude Lohuis, Vivi Rottschäfer, Cyriel M A Pennartz, Daniele Avitabile, Simon van Gaal, Umberto Olcese","doi":"10.1523/ENEURO.0191-24.2024","DOIUrl":null,"url":null,"abstract":"<p><p>Conscious reportability of visual input is associated with a bimodal neural response in the primary visual cortex (V1): an early-latency response coupled to stimulus features and a late-latency response coupled to stimulus report or detection. This late wave of activity, central to major theories of consciousness, is thought to be driven by the prefrontal cortex (PFC), responsible for \"igniting\" it. Here we analyzed two electrophysiological studies in mice performing different stimulus detection tasks and characterized neural activity profiles in three key cortical regions: V1, posterior parietal cortex (PPC), and PFC. We then developed a minimal network model, constrained by known connectivity between these regions, reproducing the spatiotemporal propagation of visual- and report-related activity. Remarkably, while PFC was indeed necessary to generate report-related activity in V1, this occurred only through the mediation of PPC. PPC, and not PFC, had the final veto in enabling the report-related late wave of V1 activity.</p>","PeriodicalId":11617,"journal":{"name":"eNeuro","volume":null,"pages":null},"PeriodicalIF":2.7000,"publicationDate":"2024-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11444237/pdf/","citationCount":"0","resultStr":"{\"title\":\"The Neural and Computational Architecture of Feedback Dynamics in Mouse Cortex during Stimulus Report.\",\"authors\":\"Simone Ciceri, Matthijs N Oude Lohuis, Vivi Rottschäfer, Cyriel M A Pennartz, Daniele Avitabile, Simon van Gaal, Umberto Olcese\",\"doi\":\"10.1523/ENEURO.0191-24.2024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Conscious reportability of visual input is associated with a bimodal neural response in the primary visual cortex (V1): an early-latency response coupled to stimulus features and a late-latency response coupled to stimulus report or detection. This late wave of activity, central to major theories of consciousness, is thought to be driven by the prefrontal cortex (PFC), responsible for \\\"igniting\\\" it. Here we analyzed two electrophysiological studies in mice performing different stimulus detection tasks and characterized neural activity profiles in three key cortical regions: V1, posterior parietal cortex (PPC), and PFC. We then developed a minimal network model, constrained by known connectivity between these regions, reproducing the spatiotemporal propagation of visual- and report-related activity. Remarkably, while PFC was indeed necessary to generate report-related activity in V1, this occurred only through the mediation of PPC. PPC, and not PFC, had the final veto in enabling the report-related late wave of V1 activity.</p>\",\"PeriodicalId\":11617,\"journal\":{\"name\":\"eNeuro\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-09-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11444237/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"eNeuro\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1523/ENEURO.0191-24.2024\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/9/1 0:00:00\",\"PubModel\":\"Print\",\"JCR\":\"Q3\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"eNeuro","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1523/ENEURO.0191-24.2024","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/1 0:00:00","PubModel":"Print","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

视觉输入的有意识可报告性与初级视觉皮层(V1)的双模神经反应有关:与刺激特征相关的早衰反应和与刺激报告或检测相关的晚衰反应。这种晚期活动波是主要意识理论的核心,被认为是由负责 "点燃 "这种活动波的前额叶皮层(PFC)驱动的。在这里,我们分析了对执行不同刺激检测任务的小鼠进行的两项电生理研究,并描述了三个关键皮层区域的神经活动特征:V1、后顶叶皮层(PPC)和前顶叶皮层。然后,我们建立了一个最小网络模型,该模型受这些区域之间已知连通性的限制,再现了视觉和报告相关活动的时空传播。值得注意的是,虽然 PFC 确实是在 V1 中产生报告相关活动的必要条件,但这只有通过 PPC 的调解才能实现。意义声明 意识研究的一个长期目标是描述与非感知的感觉刺激相比,感知的感觉刺激的神经特征。特别是,不同皮层区域在意识产生过程中的作用正在引起激烈的争论。在这里,我们结合电生理学和建模研究,探讨了大脑区域之间的单个连接在产生意识报告时所观察到的活动模式中的机理作用。我们发现,虽然额叶区启动了与报告相关的活动,但顶叶皮层则充当了决定这种活动是否会传播回视觉皮层的闸门。前额叶和顶叶皮层之间的这种分工是目前的意识理论模型所无法解释的,因此会对有意识报告的机理神经模型产生重大影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
The Neural and Computational Architecture of Feedback Dynamics in Mouse Cortex during Stimulus Report.

Conscious reportability of visual input is associated with a bimodal neural response in the primary visual cortex (V1): an early-latency response coupled to stimulus features and a late-latency response coupled to stimulus report or detection. This late wave of activity, central to major theories of consciousness, is thought to be driven by the prefrontal cortex (PFC), responsible for "igniting" it. Here we analyzed two electrophysiological studies in mice performing different stimulus detection tasks and characterized neural activity profiles in three key cortical regions: V1, posterior parietal cortex (PPC), and PFC. We then developed a minimal network model, constrained by known connectivity between these regions, reproducing the spatiotemporal propagation of visual- and report-related activity. Remarkably, while PFC was indeed necessary to generate report-related activity in V1, this occurred only through the mediation of PPC. PPC, and not PFC, had the final veto in enabling the report-related late wave of V1 activity.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
eNeuro
eNeuro Neuroscience-General Neuroscience
CiteScore
5.00
自引率
2.90%
发文量
486
审稿时长
16 weeks
期刊介绍: An open-access journal from the Society for Neuroscience, eNeuro publishes high-quality, broad-based, peer-reviewed research focused solely on the field of neuroscience. eNeuro embodies an emerging scientific vision that offers a new experience for authors and readers, all in support of the Society’s mission to advance understanding of the brain and nervous system.
期刊最新文献
Sex-Dependent Changes in Gonadotropin-Releasing Hormone Neuron Voltage-Gated Potassium Currents in a Mouse Model of Temporal Lobe Epilepsy. Bilateral Alignment of Receptive Fields in the Olfactory Cortex. Peripheral CaV2.2 channels in skin regulate prolonged heat hypersensitivity during neuroinflammation. The Neural Correlates of Spontaneous Beat Processing and Its Relationship with Music-Related Characteristics of the Individual. The Orbitofrontal Cortex Is Required for Learned Modulation of Innate Olfactory Behavior.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1