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刺激反应和抑制重复的独特相互作用的皮质网络。

Distinct interacting cortical networks for stimulus-response and repetition-suppression.

机构信息

Department of Neurology, Otto-von-Guericke University of Magdeburg, Leipziger Str. 44, 39120, Magdeburg, Germany.

Department of Behavioral Neurology, Leibniz Institute for Neurobiology, Brenneckestr. 6, 39120, Magdeburg, Germany.

出版信息

Commun Biol. 2022 Sep 5;5(1):909. doi: 10.1038/s42003-022-03861-4.

DOI:10.1038/s42003-022-03861-4
PMID:36064744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9445181/
Abstract

Non-invasive studies consider the initial neural stimulus response (SR) and repetition suppression (RS) - the decreased response to repeated sensory stimuli - as engaging the same neurons. That is, RS is a suppression of the SR. We challenge this conjecture using electrocorticographic (ECoG) recordings with high spatial resolution in ten patients listening to task-irrelevant trains of auditory stimuli. SR and RS were indexed by high-frequency activity (HFA) across temporal, parietal, and frontal cortices. HFA and HFA were temporally and spatially distinct, with HFA emerging later than HFA and showing only a limited spatial intersection with HFA: most HFA sites did not demonstrate HFA, and HFA was found where no HFA could be recorded. β activity was enhanced in HFA compared to HFA cortical sites. θ activity was enhanced in HFA compared to HFA sites. Furthermore, HFA sites propagated information to HFA sites via transient θ:β phase-phase coupling. In contrast to predictive coding (PC) accounts our results indicate that HFA and HFA are functionally linked but have minimal spatial overlap. HFA might enable stable and rapid perception of environmental stimuli across extended temporal intervals. In contrast HFA might support efficient generation of an internal model based on stimulus history.

摘要

非侵入性研究将初始神经刺激反应 (SR) 和重复抑制 (RS) 视为相同的神经元活动,RS 是对重复感觉刺激的反应减弱。我们在十名患者中使用高空间分辨率的脑电描记术 (ECoG) 记录对此进行了质疑,这些患者在听与任务无关的听觉刺激序列时会产生 RS 和 RS。SR 和 RS 通过颞叶、顶叶和额叶皮质的高频活动 (HFA) 进行索引。HFA 和 HFA 在时间和空间上是不同的,HFA 比 HFA 出现得晚,并且与 HFA 的空间交集有限:大多数 HFA 位点没有显示 HFA,而 HFA 是在没有 HFA 可以记录的地方发现的。与 HFA 相比,β 活动在 HFA 皮质位点增强。与 HFA 相比,θ 活动在 HFA 位点增强。此外,HFA 位点通过短暂的θ:β 相位-相位耦合将信息传递到 HFA 位点。与预测编码 (PC) 解释相反,我们的结果表明 HFA 和 HFA 虽然功能上相关,但空间重叠很小。HFA 可能支持在扩展的时间间隔内稳定而快速地感知环境刺激。相反,HFA 可能支持基于刺激历史的内部模型的有效生成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3315/9445181/7c720898cd66/42003_2022_3861_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3315/9445181/d34baa3d8b26/42003_2022_3861_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3315/9445181/4f4871aba8fa/42003_2022_3861_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3315/9445181/7c720898cd66/42003_2022_3861_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3315/9445181/d34baa3d8b26/42003_2022_3861_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3315/9445181/4f4871aba8fa/42003_2022_3861_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3315/9445181/7c720898cd66/42003_2022_3861_Fig3_HTML.jpg

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