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Restricting Visual Exploration Directly Impedes Neural Activity, Functional Connectivity, and Memory
We move our eyes to explore the visual world, extract information, and create memories. The number of gaze fixations—the stops that the eyes make—has been shown to correlate with activity in the hippocampus, a region critical for memory, and with later recognition memory. Here, we combined eyetracki...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595095/ https://www.ncbi.nlm.nih.gov/pubmed/33154992 http://dx.doi.org/10.1093/texcom/tgaa054 |
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author | Liu, Zhong-Xu Rosenbaum, R Shayna Ryan, Jennifer D |
author_facet | Liu, Zhong-Xu Rosenbaum, R Shayna Ryan, Jennifer D |
author_sort | Liu, Zhong-Xu |
collection | PubMed |
description | We move our eyes to explore the visual world, extract information, and create memories. The number of gaze fixations—the stops that the eyes make—has been shown to correlate with activity in the hippocampus, a region critical for memory, and with later recognition memory. Here, we combined eyetracking with fMRI to provide direct evidence for the relationships between gaze fixations, neural activity, and memory during scene viewing. Compared to free viewing, fixating a single location reduced: 1) subsequent memory, 2) neural activity along the ventral visual stream into the hippocampus, 3) neural similarity between effects of subsequent memory and visual exploration, and 4) functional connectivity among the hippocampus, parahippocampal place area, and other cortical regions. Gaze fixations were uniquely related to hippocampal activity, even after controlling for neural effects due to subsequent memory. Therefore, this study provides key causal evidence supporting the notion that the oculomotor and memory systems are intrinsically related at both the behavioral and neural level. Individual gaze fixations may provide the basic unit of information on which memory binding processes operate. |
format | Online Article Text |
id | pubmed-7595095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-75950952020-11-03 Restricting Visual Exploration Directly Impedes Neural Activity, Functional Connectivity, and Memory Liu, Zhong-Xu Rosenbaum, R Shayna Ryan, Jennifer D Cereb Cortex Commun Original Article We move our eyes to explore the visual world, extract information, and create memories. The number of gaze fixations—the stops that the eyes make—has been shown to correlate with activity in the hippocampus, a region critical for memory, and with later recognition memory. Here, we combined eyetracking with fMRI to provide direct evidence for the relationships between gaze fixations, neural activity, and memory during scene viewing. Compared to free viewing, fixating a single location reduced: 1) subsequent memory, 2) neural activity along the ventral visual stream into the hippocampus, 3) neural similarity between effects of subsequent memory and visual exploration, and 4) functional connectivity among the hippocampus, parahippocampal place area, and other cortical regions. Gaze fixations were uniquely related to hippocampal activity, even after controlling for neural effects due to subsequent memory. Therefore, this study provides key causal evidence supporting the notion that the oculomotor and memory systems are intrinsically related at both the behavioral and neural level. Individual gaze fixations may provide the basic unit of information on which memory binding processes operate. Oxford University Press 2020-08-25 /pmc/articles/PMC7595095/ /pubmed/33154992 http://dx.doi.org/10.1093/texcom/tgaa054 Text en © The Author(s) 2020. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Liu, Zhong-Xu Rosenbaum, R Shayna Ryan, Jennifer D Restricting Visual Exploration Directly Impedes Neural Activity, Functional Connectivity, and Memory |
title | Restricting Visual Exploration Directly Impedes Neural Activity, Functional Connectivity, and Memory |
title_full | Restricting Visual Exploration Directly Impedes Neural Activity, Functional Connectivity, and Memory |
title_fullStr | Restricting Visual Exploration Directly Impedes Neural Activity, Functional Connectivity, and Memory |
title_full_unstemmed | Restricting Visual Exploration Directly Impedes Neural Activity, Functional Connectivity, and Memory |
title_short | Restricting Visual Exploration Directly Impedes Neural Activity, Functional Connectivity, and Memory |
title_sort | restricting visual exploration directly impedes neural activity, functional connectivity, and memory |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595095/ https://www.ncbi.nlm.nih.gov/pubmed/33154992 http://dx.doi.org/10.1093/texcom/tgaa054 |
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