Cargando…

Neural correlates of temporal recalibration to delayed auditory feedback of active and passive movements

When we perform an action, its sensory outcomes usually follow shortly after. This characteristic temporal relationship aids in distinguishing self‐ from externally generated sensory input. To preserve this ability under dynamically changing environmental conditions, our expectation of the timing be...

Descripción completa

Detalles Bibliográficos
Autores principales: Schmitter, Christina V., Kufer, Konstantin, Steinsträter, Olaf, Sommer, Jens, Kircher, Tilo, Straube, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619381/
https://www.ncbi.nlm.nih.gov/pubmed/37818950
http://dx.doi.org/10.1002/hbm.26508
_version_ 1785129976770592768
author Schmitter, Christina V.
Kufer, Konstantin
Steinsträter, Olaf
Sommer, Jens
Kircher, Tilo
Straube, Benjamin
author_facet Schmitter, Christina V.
Kufer, Konstantin
Steinsträter, Olaf
Sommer, Jens
Kircher, Tilo
Straube, Benjamin
author_sort Schmitter, Christina V.
collection PubMed
description When we perform an action, its sensory outcomes usually follow shortly after. This characteristic temporal relationship aids in distinguishing self‐ from externally generated sensory input. To preserve this ability under dynamically changing environmental conditions, our expectation of the timing between action and outcome must be able to recalibrate, for example, when the outcome is consistently delayed. Until now, it remains unclear whether this process, known as sensorimotor temporal recalibration, can be specifically attributed to recalibration of sensorimotor (action‐outcome) predictions, or whether it may be partly due to the recalibration of expectations about the intersensory (e.g., audio‐tactile) timing. Therefore, we investigated the behavioral and neural correlates of temporal recalibration and differences in sensorimotor and intersensory contexts. During fMRI, subjects were exposed to delayed or undelayed tones elicited by actively or passively generated button presses. While recalibration of the expected intersensory timing (i.e., between the tactile sensation during the button movement and the tones) can be expected to occur during both active and passive movements, recalibration of sensorimotor predictions should be limited to active movement conditions. Effects of this procedure on auditory temporal perception and the modality‐transfer to visual perception were tested in a delay detection task. Across both contexts, we found recalibration to be associated with activations in hippocampus and cerebellum. Context‐dependent differences emerged in terms of stronger behavioral recalibration effects in sensorimotor conditions and were captured by differential activation pattern in frontal cortices, cerebellum, and sensory processing regions. These findings highlight the role of the hippocampus in encoding and retrieving newly acquired temporal stimulus associations during temporal recalibration. Furthermore, recalibration‐related activations in the cerebellum may reflect the retention of multiple representations of temporal stimulus associations across both contexts. Finally, we showed that sensorimotor predictions modulate recalibration‐related processes in frontal, cerebellar, and sensory regions, which potentially account for the perceptual advantage of sensorimotor versus intersensory temporal recalibration.
format Online
Article
Text
id pubmed-10619381
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-106193812023-11-02 Neural correlates of temporal recalibration to delayed auditory feedback of active and passive movements Schmitter, Christina V. Kufer, Konstantin Steinsträter, Olaf Sommer, Jens Kircher, Tilo Straube, Benjamin Hum Brain Mapp Research Articles When we perform an action, its sensory outcomes usually follow shortly after. This characteristic temporal relationship aids in distinguishing self‐ from externally generated sensory input. To preserve this ability under dynamically changing environmental conditions, our expectation of the timing between action and outcome must be able to recalibrate, for example, when the outcome is consistently delayed. Until now, it remains unclear whether this process, known as sensorimotor temporal recalibration, can be specifically attributed to recalibration of sensorimotor (action‐outcome) predictions, or whether it may be partly due to the recalibration of expectations about the intersensory (e.g., audio‐tactile) timing. Therefore, we investigated the behavioral and neural correlates of temporal recalibration and differences in sensorimotor and intersensory contexts. During fMRI, subjects were exposed to delayed or undelayed tones elicited by actively or passively generated button presses. While recalibration of the expected intersensory timing (i.e., between the tactile sensation during the button movement and the tones) can be expected to occur during both active and passive movements, recalibration of sensorimotor predictions should be limited to active movement conditions. Effects of this procedure on auditory temporal perception and the modality‐transfer to visual perception were tested in a delay detection task. Across both contexts, we found recalibration to be associated with activations in hippocampus and cerebellum. Context‐dependent differences emerged in terms of stronger behavioral recalibration effects in sensorimotor conditions and were captured by differential activation pattern in frontal cortices, cerebellum, and sensory processing regions. These findings highlight the role of the hippocampus in encoding and retrieving newly acquired temporal stimulus associations during temporal recalibration. Furthermore, recalibration‐related activations in the cerebellum may reflect the retention of multiple representations of temporal stimulus associations across both contexts. Finally, we showed that sensorimotor predictions modulate recalibration‐related processes in frontal, cerebellar, and sensory regions, which potentially account for the perceptual advantage of sensorimotor versus intersensory temporal recalibration. John Wiley & Sons, Inc. 2023-10-11 /pmc/articles/PMC10619381/ /pubmed/37818950 http://dx.doi.org/10.1002/hbm.26508 Text en © 2023 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Schmitter, Christina V.
Kufer, Konstantin
Steinsträter, Olaf
Sommer, Jens
Kircher, Tilo
Straube, Benjamin
Neural correlates of temporal recalibration to delayed auditory feedback of active and passive movements
title Neural correlates of temporal recalibration to delayed auditory feedback of active and passive movements
title_full Neural correlates of temporal recalibration to delayed auditory feedback of active and passive movements
title_fullStr Neural correlates of temporal recalibration to delayed auditory feedback of active and passive movements
title_full_unstemmed Neural correlates of temporal recalibration to delayed auditory feedback of active and passive movements
title_short Neural correlates of temporal recalibration to delayed auditory feedback of active and passive movements
title_sort neural correlates of temporal recalibration to delayed auditory feedback of active and passive movements
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619381/
https://www.ncbi.nlm.nih.gov/pubmed/37818950
http://dx.doi.org/10.1002/hbm.26508
work_keys_str_mv AT schmitterchristinav neuralcorrelatesoftemporalrecalibrationtodelayedauditoryfeedbackofactiveandpassivemovements
AT kuferkonstantin neuralcorrelatesoftemporalrecalibrationtodelayedauditoryfeedbackofactiveandpassivemovements
AT steinstraterolaf neuralcorrelatesoftemporalrecalibrationtodelayedauditoryfeedbackofactiveandpassivemovements
AT sommerjens neuralcorrelatesoftemporalrecalibrationtodelayedauditoryfeedbackofactiveandpassivemovements
AT kirchertilo neuralcorrelatesoftemporalrecalibrationtodelayedauditoryfeedbackofactiveandpassivemovements
AT straubebenjamin neuralcorrelatesoftemporalrecalibrationtodelayedauditoryfeedbackofactiveandpassivemovements