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Specific sensorimotor interneuron circuits are sensitive to cerebellar-attention interactions

Background: Short latency afferent inhibition (SAI) provides a method to investigate mechanisms of sensorimotor integration. Cholinergic involvement in the SAI phenomena suggests that SAI may provide a marker of cognitive influence over implicit sensorimotor processes. Consistent with this hypothesi...

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Autores principales: Mirdamadi, Jasmine L., Meehan, Sean K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437336/
https://www.ncbi.nlm.nih.gov/pubmed/36061499
http://dx.doi.org/10.3389/fnhum.2022.920526
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author Mirdamadi, Jasmine L.
Meehan, Sean K.
author_facet Mirdamadi, Jasmine L.
Meehan, Sean K.
author_sort Mirdamadi, Jasmine L.
collection PubMed
description Background: Short latency afferent inhibition (SAI) provides a method to investigate mechanisms of sensorimotor integration. Cholinergic involvement in the SAI phenomena suggests that SAI may provide a marker of cognitive influence over implicit sensorimotor processes. Consistent with this hypothesis, we previously demonstrated that visual attention load suppresses SAI circuits preferentially recruited by anterior-to-posterior (AP)-, but not posterior-to-anterior (PA)-current induced by transcranial magnetic stimulation. However, cerebellar modulation can also modulate these same AP-sensitive SAI circuits. Yet, the consequences of concurrent cognitive and implicit cerebellar influences over these AP circuits are unknown. Objective: We used cerebellar intermittent theta-burst stimulation (iTBS) to determine whether the cerebellar modulation of sensory to motor projections interacts with the attentional modulation of sensory to motor circuits probed by SAI. Methods: We assessed AP-SAI and PA-SAI during a concurrent visual detection task of varying attention load before and after cerebellar iTBS. Results: Before cerebellar iTBS, a higher visual attention load suppressed AP-SAI, but not PA-SAI, compared to a lower visual attention load. Post-cerebellar iTBS, the pattern of AP-SAI in response to visual attention load, was reversed; a higher visual attention load enhanced AP-SAI compared to a lower visual attention load. Cerebellar iTBS did not affect PA-SAI regardless of visual attention load. Conclusion: These findings suggest that attention and cerebellar networks converge on overlapping AP-sensitive circuitry to influence motor output by controlling the strength of the afferent projections to the motor cortex. This interaction has important implications for understanding the mechanisms of motor performance and learning.
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spelling pubmed-94373362022-09-03 Specific sensorimotor interneuron circuits are sensitive to cerebellar-attention interactions Mirdamadi, Jasmine L. Meehan, Sean K. Front Hum Neurosci Human Neuroscience Background: Short latency afferent inhibition (SAI) provides a method to investigate mechanisms of sensorimotor integration. Cholinergic involvement in the SAI phenomena suggests that SAI may provide a marker of cognitive influence over implicit sensorimotor processes. Consistent with this hypothesis, we previously demonstrated that visual attention load suppresses SAI circuits preferentially recruited by anterior-to-posterior (AP)-, but not posterior-to-anterior (PA)-current induced by transcranial magnetic stimulation. However, cerebellar modulation can also modulate these same AP-sensitive SAI circuits. Yet, the consequences of concurrent cognitive and implicit cerebellar influences over these AP circuits are unknown. Objective: We used cerebellar intermittent theta-burst stimulation (iTBS) to determine whether the cerebellar modulation of sensory to motor projections interacts with the attentional modulation of sensory to motor circuits probed by SAI. Methods: We assessed AP-SAI and PA-SAI during a concurrent visual detection task of varying attention load before and after cerebellar iTBS. Results: Before cerebellar iTBS, a higher visual attention load suppressed AP-SAI, but not PA-SAI, compared to a lower visual attention load. Post-cerebellar iTBS, the pattern of AP-SAI in response to visual attention load, was reversed; a higher visual attention load enhanced AP-SAI compared to a lower visual attention load. Cerebellar iTBS did not affect PA-SAI regardless of visual attention load. Conclusion: These findings suggest that attention and cerebellar networks converge on overlapping AP-sensitive circuitry to influence motor output by controlling the strength of the afferent projections to the motor cortex. This interaction has important implications for understanding the mechanisms of motor performance and learning. Frontiers Media S.A. 2022-08-19 /pmc/articles/PMC9437336/ /pubmed/36061499 http://dx.doi.org/10.3389/fnhum.2022.920526 Text en Copyright © 2022 Mirdamadi and Meehan. https://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
Mirdamadi, Jasmine L.
Meehan, Sean K.
Specific sensorimotor interneuron circuits are sensitive to cerebellar-attention interactions
title Specific sensorimotor interneuron circuits are sensitive to cerebellar-attention interactions
title_full Specific sensorimotor interneuron circuits are sensitive to cerebellar-attention interactions
title_fullStr Specific sensorimotor interneuron circuits are sensitive to cerebellar-attention interactions
title_full_unstemmed Specific sensorimotor interneuron circuits are sensitive to cerebellar-attention interactions
title_short Specific sensorimotor interneuron circuits are sensitive to cerebellar-attention interactions
title_sort specific sensorimotor interneuron circuits are sensitive to cerebellar-attention interactions
topic Human Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437336/
https://www.ncbi.nlm.nih.gov/pubmed/36061499
http://dx.doi.org/10.3389/fnhum.2022.920526
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