Neural activity in the human anterior thalamus during natural vision

Abstract In natural vision humans and other primates explore environment by active sensing, using saccadic eye movements to relocate the fovea and sample different bits of information multiple times per second. Saccades induce a phase reset of ongoing neuronal oscillations in primary and higher-orde...

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Autores principales: Marcin Leszczynski, Leila Chaieb, Tobias Staudigl, Simon Jonas Enkirch, Juergen Fell, Charles E. Schroeder
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:551408da270344888da64bc8098ce4862021-12-02T19:04:19ZNeural activity in the human anterior thalamus during natural vision10.1038/s41598-021-96588-x2045-2322https://doaj.org/article/551408da270344888da64bc8098ce4862021-09-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-96588-xhttps://doaj.org/toc/2045-2322Abstract In natural vision humans and other primates explore environment by active sensing, using saccadic eye movements to relocate the fovea and sample different bits of information multiple times per second. Saccades induce a phase reset of ongoing neuronal oscillations in primary and higher-order visual cortices and in the medial temporal lobe. As a result, neuron ensembles are shifted to a common state at the time visual input propagates through the system (i.e., just after fixation). The extent of the brain’s circuitry that is modulated by saccades is not yet known. Here, we evaluate the possibility that saccadic phase reset impacts the anterior nuclei of the thalamus (ANT). Using recordings in the human thalamus of three surgical patients during natural vision, we found that saccades and visual stimulus onset both modulate neural activity, but with distinct field potential morphologies. Specifically, we found that fixation-locked field potentials had a component that preceded saccade onset. It was followed by an early negativity around 50 ms after fixation onset which is significantly faster than any response to visual stimulus presentation. The timing of these events suggests that the ANT is predictively modulated before the saccadic eye movement. We also found oscillatory phase concentration, peaking at 3–4 Hz, coincident with suppression of Broadband High-frequency Activity (BHA; 80–180 Hz), both locked to fixation onset supporting the idea that neural oscillations in these nuclei are reorganized to a low excitability state right after fixation onset. These findings show that during real-world natural visual exploration neural dynamics in the human ANT is influenced by visual and oculomotor events, which supports the idea that ANT, apart from their contribution to episodic memory, also play a role in natural vision.Marcin LeszczynskiLeila ChaiebTobias StaudiglSimon Jonas EnkirchJuergen FellCharles E. SchroederNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Marcin Leszczynski
Leila Chaieb
Tobias Staudigl
Simon Jonas Enkirch
Juergen Fell
Charles E. Schroeder
Neural activity in the human anterior thalamus during natural vision
description Abstract In natural vision humans and other primates explore environment by active sensing, using saccadic eye movements to relocate the fovea and sample different bits of information multiple times per second. Saccades induce a phase reset of ongoing neuronal oscillations in primary and higher-order visual cortices and in the medial temporal lobe. As a result, neuron ensembles are shifted to a common state at the time visual input propagates through the system (i.e., just after fixation). The extent of the brain’s circuitry that is modulated by saccades is not yet known. Here, we evaluate the possibility that saccadic phase reset impacts the anterior nuclei of the thalamus (ANT). Using recordings in the human thalamus of three surgical patients during natural vision, we found that saccades and visual stimulus onset both modulate neural activity, but with distinct field potential morphologies. Specifically, we found that fixation-locked field potentials had a component that preceded saccade onset. It was followed by an early negativity around 50 ms after fixation onset which is significantly faster than any response to visual stimulus presentation. The timing of these events suggests that the ANT is predictively modulated before the saccadic eye movement. We also found oscillatory phase concentration, peaking at 3–4 Hz, coincident with suppression of Broadband High-frequency Activity (BHA; 80–180 Hz), both locked to fixation onset supporting the idea that neural oscillations in these nuclei are reorganized to a low excitability state right after fixation onset. These findings show that during real-world natural visual exploration neural dynamics in the human ANT is influenced by visual and oculomotor events, which supports the idea that ANT, apart from their contribution to episodic memory, also play a role in natural vision.
format article
author Marcin Leszczynski
Leila Chaieb
Tobias Staudigl
Simon Jonas Enkirch
Juergen Fell
Charles E. Schroeder
author_facet Marcin Leszczynski
Leila Chaieb
Tobias Staudigl
Simon Jonas Enkirch
Juergen Fell
Charles E. Schroeder
author_sort Marcin Leszczynski
title Neural activity in the human anterior thalamus during natural vision
title_short Neural activity in the human anterior thalamus during natural vision
title_full Neural activity in the human anterior thalamus during natural vision
title_fullStr Neural activity in the human anterior thalamus during natural vision
title_full_unstemmed Neural activity in the human anterior thalamus during natural vision
title_sort neural activity in the human anterior thalamus during natural vision
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/551408da270344888da64bc8098ce486
work_keys_str_mv AT marcinleszczynski neuralactivityinthehumananteriorthalamusduringnaturalvision
AT leilachaieb neuralactivityinthehumananteriorthalamusduringnaturalvision
AT tobiasstaudigl neuralactivityinthehumananteriorthalamusduringnaturalvision
AT simonjonasenkirch neuralactivityinthehumananteriorthalamusduringnaturalvision
AT juergenfell neuralactivityinthehumananteriorthalamusduringnaturalvision
AT charleseschroeder neuralactivityinthehumananteriorthalamusduringnaturalvision
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