Cargando…
Neural excitability and sensory input determine intensity perception with opposing directions in initial cortical responses
Perception of sensory information is determined by stimulus features (e.g., intensity) and instantaneous neural states (e.g., excitability). Commonly, it is assumed that both are reflected similarly in evoked brain potentials, that is, larger amplitudes are associated with a stronger percept of a st...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492057/ https://www.ncbi.nlm.nih.gov/pubmed/34609278 http://dx.doi.org/10.7554/eLife.67838 |
_version_ | 1784578854256377856 |
---|---|
author | Stephani, Tilman Hodapp, Alice Jamshidi Idaji, Mina Villringer, Arno Nikulin, Vadim V |
author_facet | Stephani, Tilman Hodapp, Alice Jamshidi Idaji, Mina Villringer, Arno Nikulin, Vadim V |
author_sort | Stephani, Tilman |
collection | PubMed |
description | Perception of sensory information is determined by stimulus features (e.g., intensity) and instantaneous neural states (e.g., excitability). Commonly, it is assumed that both are reflected similarly in evoked brain potentials, that is, larger amplitudes are associated with a stronger percept of a stimulus. We tested this assumption in a somatosensory discrimination task in humans, simultaneously assessing (i) single-trial excitatory post-synaptic currents inferred from short-latency somatosensory evoked potentials (SEPs), (ii) pre-stimulus alpha oscillations (8–13 Hz), and (iii) peripheral nerve measures. Fluctuations of neural excitability shaped the perceived stimulus intensity already during the very first cortical response (at ~20 ms) yet demonstrating opposite neural signatures as compared to the effect of presented stimulus intensity. We reconcile this discrepancy via a common framework based on the modulation of electro-chemical membrane gradients linking neural states and responses, which calls for reconsidering conventional interpretations of brain potential magnitudes in stimulus intensity encoding. |
format | Online Article Text |
id | pubmed-8492057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-84920572021-10-06 Neural excitability and sensory input determine intensity perception with opposing directions in initial cortical responses Stephani, Tilman Hodapp, Alice Jamshidi Idaji, Mina Villringer, Arno Nikulin, Vadim V eLife Neuroscience Perception of sensory information is determined by stimulus features (e.g., intensity) and instantaneous neural states (e.g., excitability). Commonly, it is assumed that both are reflected similarly in evoked brain potentials, that is, larger amplitudes are associated with a stronger percept of a stimulus. We tested this assumption in a somatosensory discrimination task in humans, simultaneously assessing (i) single-trial excitatory post-synaptic currents inferred from short-latency somatosensory evoked potentials (SEPs), (ii) pre-stimulus alpha oscillations (8–13 Hz), and (iii) peripheral nerve measures. Fluctuations of neural excitability shaped the perceived stimulus intensity already during the very first cortical response (at ~20 ms) yet demonstrating opposite neural signatures as compared to the effect of presented stimulus intensity. We reconcile this discrepancy via a common framework based on the modulation of electro-chemical membrane gradients linking neural states and responses, which calls for reconsidering conventional interpretations of brain potential magnitudes in stimulus intensity encoding. eLife Sciences Publications, Ltd 2021-10-05 /pmc/articles/PMC8492057/ /pubmed/34609278 http://dx.doi.org/10.7554/eLife.67838 Text en © 2021, Stephani et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Stephani, Tilman Hodapp, Alice Jamshidi Idaji, Mina Villringer, Arno Nikulin, Vadim V Neural excitability and sensory input determine intensity perception with opposing directions in initial cortical responses |
title | Neural excitability and sensory input determine intensity perception with opposing directions in initial cortical responses |
title_full | Neural excitability and sensory input determine intensity perception with opposing directions in initial cortical responses |
title_fullStr | Neural excitability and sensory input determine intensity perception with opposing directions in initial cortical responses |
title_full_unstemmed | Neural excitability and sensory input determine intensity perception with opposing directions in initial cortical responses |
title_short | Neural excitability and sensory input determine intensity perception with opposing directions in initial cortical responses |
title_sort | neural excitability and sensory input determine intensity perception with opposing directions in initial cortical responses |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492057/ https://www.ncbi.nlm.nih.gov/pubmed/34609278 http://dx.doi.org/10.7554/eLife.67838 |
work_keys_str_mv | AT stephanitilman neuralexcitabilityandsensoryinputdetermineintensityperceptionwithopposingdirectionsininitialcorticalresponses AT hodappalice neuralexcitabilityandsensoryinputdetermineintensityperceptionwithopposingdirectionsininitialcorticalresponses AT jamshidiidajimina neuralexcitabilityandsensoryinputdetermineintensityperceptionwithopposingdirectionsininitialcorticalresponses AT villringerarno neuralexcitabilityandsensoryinputdetermineintensityperceptionwithopposingdirectionsininitialcorticalresponses AT nikulinvadimv neuralexcitabilityandsensoryinputdetermineintensityperceptionwithopposingdirectionsininitialcorticalresponses |