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Occipital Magnocellular VEP Non-linearities Show a Short Latency Interaction Between Contrast and Facial Emotion
The magnocellular system has been implicated in the rapid processing of facial emotions, such as fear. Of the various anatomical possibilities, the retino-colliculo-pulvinar route to the amygdala is currently favored. However, it is not clear whether and when amygdala arousal activates the primary v...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381315/ https://www.ncbi.nlm.nih.gov/pubmed/32754021 http://dx.doi.org/10.3389/fnhum.2020.00268 |
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author | Mu, Eveline Crewther, David |
author_facet | Mu, Eveline Crewther, David |
author_sort | Mu, Eveline |
collection | PubMed |
description | The magnocellular system has been implicated in the rapid processing of facial emotions, such as fear. Of the various anatomical possibilities, the retino-colliculo-pulvinar route to the amygdala is currently favored. However, it is not clear whether and when amygdala arousal activates the primary visual cortex (V1). Non-linear visual evoked potentials provide a well-accepted technique for examining temporal processing in the magnocellular and parvocellular pathways in the visual cortex. Here, we investigated the relationship between facial emotion processing and the separable magnocellular (K2.1) and parvocellular (K2.2) components of the second-order non-linear multifocal visual evoked potential responses recorded from the occipital scalp (O(Z)). Stimuli comprised pseudorandom brightening/darkening of fearful, happy, neutral faces (or no face) with surround patches decorrelated from the central face-bearing patch. For the central patch, the spatial contrast of the faces was 30% while the modulation of the per-pixel brightening/darkening was uniformly 10% or 70%. From 14 neurotypical young adults, we found a significant interaction between emotion and contrast in the magnocellularly driven K2.1 peak amplitudes, with greater K2.1 amplitudes for fearful (vs. happy) faces at 70% temporal contrast condition. Taken together, our findings suggest that facial emotional information is present in early V1 processing as conveyed by the M pathway, and more activated for fearful as opposed to happy and neutral faces. An explanation is offered in terms of the contest between feedback and response gain modulation models. |
format | Online Article Text |
id | pubmed-7381315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73813152020-08-03 Occipital Magnocellular VEP Non-linearities Show a Short Latency Interaction Between Contrast and Facial Emotion Mu, Eveline Crewther, David Front Hum Neurosci Human Neuroscience The magnocellular system has been implicated in the rapid processing of facial emotions, such as fear. Of the various anatomical possibilities, the retino-colliculo-pulvinar route to the amygdala is currently favored. However, it is not clear whether and when amygdala arousal activates the primary visual cortex (V1). Non-linear visual evoked potentials provide a well-accepted technique for examining temporal processing in the magnocellular and parvocellular pathways in the visual cortex. Here, we investigated the relationship between facial emotion processing and the separable magnocellular (K2.1) and parvocellular (K2.2) components of the second-order non-linear multifocal visual evoked potential responses recorded from the occipital scalp (O(Z)). Stimuli comprised pseudorandom brightening/darkening of fearful, happy, neutral faces (or no face) with surround patches decorrelated from the central face-bearing patch. For the central patch, the spatial contrast of the faces was 30% while the modulation of the per-pixel brightening/darkening was uniformly 10% or 70%. From 14 neurotypical young adults, we found a significant interaction between emotion and contrast in the magnocellularly driven K2.1 peak amplitudes, with greater K2.1 amplitudes for fearful (vs. happy) faces at 70% temporal contrast condition. Taken together, our findings suggest that facial emotional information is present in early V1 processing as conveyed by the M pathway, and more activated for fearful as opposed to happy and neutral faces. An explanation is offered in terms of the contest between feedback and response gain modulation models. Frontiers Media S.A. 2020-07-09 /pmc/articles/PMC7381315/ /pubmed/32754021 http://dx.doi.org/10.3389/fnhum.2020.00268 Text en Copyright © 2020 Mu and Crewther. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Human Neuroscience Mu, Eveline Crewther, David Occipital Magnocellular VEP Non-linearities Show a Short Latency Interaction Between Contrast and Facial Emotion |
title | Occipital Magnocellular VEP Non-linearities Show a Short Latency Interaction Between Contrast and Facial Emotion |
title_full | Occipital Magnocellular VEP Non-linearities Show a Short Latency Interaction Between Contrast and Facial Emotion |
title_fullStr | Occipital Magnocellular VEP Non-linearities Show a Short Latency Interaction Between Contrast and Facial Emotion |
title_full_unstemmed | Occipital Magnocellular VEP Non-linearities Show a Short Latency Interaction Between Contrast and Facial Emotion |
title_short | Occipital Magnocellular VEP Non-linearities Show a Short Latency Interaction Between Contrast and Facial Emotion |
title_sort | occipital magnocellular vep non-linearities show a short latency interaction between contrast and facial emotion |
topic | Human Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381315/ https://www.ncbi.nlm.nih.gov/pubmed/32754021 http://dx.doi.org/10.3389/fnhum.2020.00268 |
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