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The sequence of cortical activity inferred by response latency variability in the human ventral pathway of face processing

Variability in neuronal response latency has been typically considered caused by random noise. Previous studies of single cells and large neuronal populations have shown that the temporal variability tends to increase along the visual pathway. Inspired by these previous studies, we hypothesized that...

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Autores principales: Lin, Jo-Fu Lotus, Silva-Pereyra, Juan, Chou, Chih-Che, Lin, Fa-Hsuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895585/
https://www.ncbi.nlm.nih.gov/pubmed/29643441
http://dx.doi.org/10.1038/s41598-018-23942-x
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author Lin, Jo-Fu Lotus
Silva-Pereyra, Juan
Chou, Chih-Che
Lin, Fa-Hsuan
author_facet Lin, Jo-Fu Lotus
Silva-Pereyra, Juan
Chou, Chih-Che
Lin, Fa-Hsuan
author_sort Lin, Jo-Fu Lotus
collection PubMed
description Variability in neuronal response latency has been typically considered caused by random noise. Previous studies of single cells and large neuronal populations have shown that the temporal variability tends to increase along the visual pathway. Inspired by these previous studies, we hypothesized that functional areas at later stages in the visual pathway of face processing would have larger variability in the response latency. To test this hypothesis, we used magnetoencephalographic data collected when subjects were presented with images of human faces. Faces are known to elicit a sequence of activity from the primary visual cortex to the fusiform gyrus. Our results revealed that the fusiform gyrus showed larger variability in the response latency compared to the calcarine fissure. Dynamic and spectral analyses of the latency variability indicated that the response latency in the fusiform gyrus was more variable than in the calcarine fissure between 70 ms and 200 ms after the stimulus onset and between 4 Hz and 40 Hz, respectively. The sequential processing of face information from the calcarine sulcus to the fusiform sulcus was more reliably detected based on sizes of the response variability than instants of the maximal response peaks. With two areas in the ventral visual pathway, we show that the variability in response latency across brain areas can be used to infer the sequence of cortical activity.
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spelling pubmed-58955852018-04-12 The sequence of cortical activity inferred by response latency variability in the human ventral pathway of face processing Lin, Jo-Fu Lotus Silva-Pereyra, Juan Chou, Chih-Che Lin, Fa-Hsuan Sci Rep Article Variability in neuronal response latency has been typically considered caused by random noise. Previous studies of single cells and large neuronal populations have shown that the temporal variability tends to increase along the visual pathway. Inspired by these previous studies, we hypothesized that functional areas at later stages in the visual pathway of face processing would have larger variability in the response latency. To test this hypothesis, we used magnetoencephalographic data collected when subjects were presented with images of human faces. Faces are known to elicit a sequence of activity from the primary visual cortex to the fusiform gyrus. Our results revealed that the fusiform gyrus showed larger variability in the response latency compared to the calcarine fissure. Dynamic and spectral analyses of the latency variability indicated that the response latency in the fusiform gyrus was more variable than in the calcarine fissure between 70 ms and 200 ms after the stimulus onset and between 4 Hz and 40 Hz, respectively. The sequential processing of face information from the calcarine sulcus to the fusiform sulcus was more reliably detected based on sizes of the response variability than instants of the maximal response peaks. With two areas in the ventral visual pathway, we show that the variability in response latency across brain areas can be used to infer the sequence of cortical activity. Nature Publishing Group UK 2018-04-11 /pmc/articles/PMC5895585/ /pubmed/29643441 http://dx.doi.org/10.1038/s41598-018-23942-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lin, Jo-Fu Lotus
Silva-Pereyra, Juan
Chou, Chih-Che
Lin, Fa-Hsuan
The sequence of cortical activity inferred by response latency variability in the human ventral pathway of face processing
title The sequence of cortical activity inferred by response latency variability in the human ventral pathway of face processing
title_full The sequence of cortical activity inferred by response latency variability in the human ventral pathway of face processing
title_fullStr The sequence of cortical activity inferred by response latency variability in the human ventral pathway of face processing
title_full_unstemmed The sequence of cortical activity inferred by response latency variability in the human ventral pathway of face processing
title_short The sequence of cortical activity inferred by response latency variability in the human ventral pathway of face processing
title_sort sequence of cortical activity inferred by response latency variability in the human ventral pathway of face processing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895585/
https://www.ncbi.nlm.nih.gov/pubmed/29643441
http://dx.doi.org/10.1038/s41598-018-23942-x
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