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Tuning Eye-Gaze Perception by Transitory STS Inhibition
Processing eye-gaze information is a key step to human social interaction. Neuroimaging studies have shown that superior temporal sulcus (STS) is highly implicated in eye-gaze perception. In autism, a lack of preference for the eyes, as well as anatomo-functional abnormalities within the STS, has be...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869819/ https://www.ncbi.nlm.nih.gov/pubmed/26946130 http://dx.doi.org/10.1093/cercor/bhw045 |
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author | Saitovitch, Ana Popa, Traian Lemaitre, Hervé Rechtman, Elza Lamy, Jean-Charles Grévent, David Calmon, Raphael Meunier, Sabine Brunelle, Francis Samson, Yves Boddaert, Nathalie Zilbovicius, Monica |
author_facet | Saitovitch, Ana Popa, Traian Lemaitre, Hervé Rechtman, Elza Lamy, Jean-Charles Grévent, David Calmon, Raphael Meunier, Sabine Brunelle, Francis Samson, Yves Boddaert, Nathalie Zilbovicius, Monica |
author_sort | Saitovitch, Ana |
collection | PubMed |
description | Processing eye-gaze information is a key step to human social interaction. Neuroimaging studies have shown that superior temporal sulcus (STS) is highly implicated in eye-gaze perception. In autism, a lack of preference for the eyes, as well as anatomo-functional abnormalities within the STS, has been described. To date, there are no experimental data in humans showing whether it is possible to interfere with eye-gaze processing by modulating STS neural activity. Here, we measured eye-gaze perception before and after inhibitory transcranial magnetic stimulation (TMS) applied over the posterior STS (pSTS) in young healthy volunteers. Eye-gaze processing, namely overt orienting toward the eyes, was measured using eye tracking during passive visualization of social movies. Inhibition of the right pSTS led participants to look less to the eyes of characters during visualization of social movies. Such effect was specific for the eyes and was not observed after inhibition of the left pSTS nor after placebo TMS. These results indicate for the first time that interfering with the right pSTS neural activity transitorily disrupts the behavior of orienting toward the eyes and thus indirectly gaze perception, a fundamental process for human social cognition. These results could open up new perspectives in therapeutic interventions in autism. |
format | Online Article Text |
id | pubmed-4869819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48698192016-05-26 Tuning Eye-Gaze Perception by Transitory STS Inhibition Saitovitch, Ana Popa, Traian Lemaitre, Hervé Rechtman, Elza Lamy, Jean-Charles Grévent, David Calmon, Raphael Meunier, Sabine Brunelle, Francis Samson, Yves Boddaert, Nathalie Zilbovicius, Monica Cereb Cortex Articles Processing eye-gaze information is a key step to human social interaction. Neuroimaging studies have shown that superior temporal sulcus (STS) is highly implicated in eye-gaze perception. In autism, a lack of preference for the eyes, as well as anatomo-functional abnormalities within the STS, has been described. To date, there are no experimental data in humans showing whether it is possible to interfere with eye-gaze processing by modulating STS neural activity. Here, we measured eye-gaze perception before and after inhibitory transcranial magnetic stimulation (TMS) applied over the posterior STS (pSTS) in young healthy volunteers. Eye-gaze processing, namely overt orienting toward the eyes, was measured using eye tracking during passive visualization of social movies. Inhibition of the right pSTS led participants to look less to the eyes of characters during visualization of social movies. Such effect was specific for the eyes and was not observed after inhibition of the left pSTS nor after placebo TMS. These results indicate for the first time that interfering with the right pSTS neural activity transitorily disrupts the behavior of orienting toward the eyes and thus indirectly gaze perception, a fundamental process for human social cognition. These results could open up new perspectives in therapeutic interventions in autism. Oxford University Press 2016-06 2016-03-05 /pmc/articles/PMC4869819/ /pubmed/26946130 http://dx.doi.org/10.1093/cercor/bhw045 Text en © The Author 2016. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Articles Saitovitch, Ana Popa, Traian Lemaitre, Hervé Rechtman, Elza Lamy, Jean-Charles Grévent, David Calmon, Raphael Meunier, Sabine Brunelle, Francis Samson, Yves Boddaert, Nathalie Zilbovicius, Monica Tuning Eye-Gaze Perception by Transitory STS Inhibition |
title | Tuning Eye-Gaze Perception by Transitory STS Inhibition |
title_full | Tuning Eye-Gaze Perception by Transitory STS Inhibition |
title_fullStr | Tuning Eye-Gaze Perception by Transitory STS Inhibition |
title_full_unstemmed | Tuning Eye-Gaze Perception by Transitory STS Inhibition |
title_short | Tuning Eye-Gaze Perception by Transitory STS Inhibition |
title_sort | tuning eye-gaze perception by transitory sts inhibition |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869819/ https://www.ncbi.nlm.nih.gov/pubmed/26946130 http://dx.doi.org/10.1093/cercor/bhw045 |
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