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Spatial and Temporal Arrangement of Recurrent Inhibition in the Primate Upper Limb

Renshaw cells mediate recurrent inhibition between motoneurons within the spinal cord. The function of this circuit is not clear; we previously suggested based on computational modeling that it may cancel oscillations in muscle activity around 10 Hz, thereby reducing physiological tremor. Such tremo...

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Autores principales: Edgley, Steve A., Williams, Elizabeth R., Baker, Stuart N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896010/
https://www.ncbi.nlm.nih.gov/pubmed/33334866
http://dx.doi.org/10.1523/JNEUROSCI.1589-20.2020
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author Edgley, Steve A.
Williams, Elizabeth R.
Baker, Stuart N.
author_facet Edgley, Steve A.
Williams, Elizabeth R.
Baker, Stuart N.
author_sort Edgley, Steve A.
collection PubMed
description Renshaw cells mediate recurrent inhibition between motoneurons within the spinal cord. The function of this circuit is not clear; we previously suggested based on computational modeling that it may cancel oscillations in muscle activity around 10 Hz, thereby reducing physiological tremor. Such tremor is especially problematic for dexterous hand movements, yet knowledge of recurrent inhibitory function is sparse for the control of the primate upper limb, where no direct measurements have been made to date. In this study, we made intracellular penetrations into 89 motoneurons in the cervical enlargement of four terminally anesthetized female macaque monkeys, and recorded recurrent IPSPs in response to antidromic stimulation of motor axons. Recurrent inhibition was strongest to motoneurons innervating shoulder muscles and elbow extensors, weak to wrist and digit extensors, and almost absent to the intrinsic muscles of the hand. Recurrent inhibitory connections often spanned joints, for example from motoneurons innervating wrist and digit muscles to those controlling the shoulder and elbow. Wrist and digit flexor motoneurons sometimes inhibited the corresponding extensors, and vice versa. This complex connectivity presumably reflects the flexible usage of the primate upper limb. Using trains of stimuli to motor nerves timed as a Poisson process and coherence analysis, we also examined the temporal properties of recurrent inhibition. The recurrent feedback loop effectively carried frequencies up to 100 Hz, with a coherence peak around 20 Hz. The coherence phase validated predictions from our previous computational model, supporting the idea that recurrent inhibition may function to reduce tremor. SIGNIFICANCE STATEMENT We present the first direct measurements of recurrent inhibition in primate upper limb motoneurons, revealing that it is more flexibly organized than previous observations in cat. Recurrent inhibitory connections were relatively common between motoneurons controlling muscles that act at different joints, and between flexors and extensors. As in the cat, connections were minimal for motoneurons innervating the most distal intrinsic hand muscles. Empirical data are consistent with previous modeling: temporal properties of the recurrent inhibitory feedback loop are compatible with a role in reducing physiological tremor by suppressing oscillations around 10 Hz.
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spelling pubmed-78960102021-02-22 Spatial and Temporal Arrangement of Recurrent Inhibition in the Primate Upper Limb Edgley, Steve A. Williams, Elizabeth R. Baker, Stuart N. J Neurosci Research Articles Renshaw cells mediate recurrent inhibition between motoneurons within the spinal cord. The function of this circuit is not clear; we previously suggested based on computational modeling that it may cancel oscillations in muscle activity around 10 Hz, thereby reducing physiological tremor. Such tremor is especially problematic for dexterous hand movements, yet knowledge of recurrent inhibitory function is sparse for the control of the primate upper limb, where no direct measurements have been made to date. In this study, we made intracellular penetrations into 89 motoneurons in the cervical enlargement of four terminally anesthetized female macaque monkeys, and recorded recurrent IPSPs in response to antidromic stimulation of motor axons. Recurrent inhibition was strongest to motoneurons innervating shoulder muscles and elbow extensors, weak to wrist and digit extensors, and almost absent to the intrinsic muscles of the hand. Recurrent inhibitory connections often spanned joints, for example from motoneurons innervating wrist and digit muscles to those controlling the shoulder and elbow. Wrist and digit flexor motoneurons sometimes inhibited the corresponding extensors, and vice versa. This complex connectivity presumably reflects the flexible usage of the primate upper limb. Using trains of stimuli to motor nerves timed as a Poisson process and coherence analysis, we also examined the temporal properties of recurrent inhibition. The recurrent feedback loop effectively carried frequencies up to 100 Hz, with a coherence peak around 20 Hz. The coherence phase validated predictions from our previous computational model, supporting the idea that recurrent inhibition may function to reduce tremor. SIGNIFICANCE STATEMENT We present the first direct measurements of recurrent inhibition in primate upper limb motoneurons, revealing that it is more flexibly organized than previous observations in cat. Recurrent inhibitory connections were relatively common between motoneurons controlling muscles that act at different joints, and between flexors and extensors. As in the cat, connections were minimal for motoneurons innervating the most distal intrinsic hand muscles. Empirical data are consistent with previous modeling: temporal properties of the recurrent inhibitory feedback loop are compatible with a role in reducing physiological tremor by suppressing oscillations around 10 Hz. Society for Neuroscience 2021-02-17 /pmc/articles/PMC7896010/ /pubmed/33334866 http://dx.doi.org/10.1523/JNEUROSCI.1589-20.2020 Text en Copyright © 2021 Edgley et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Articles
Edgley, Steve A.
Williams, Elizabeth R.
Baker, Stuart N.
Spatial and Temporal Arrangement of Recurrent Inhibition in the Primate Upper Limb
title Spatial and Temporal Arrangement of Recurrent Inhibition in the Primate Upper Limb
title_full Spatial and Temporal Arrangement of Recurrent Inhibition in the Primate Upper Limb
title_fullStr Spatial and Temporal Arrangement of Recurrent Inhibition in the Primate Upper Limb
title_full_unstemmed Spatial and Temporal Arrangement of Recurrent Inhibition in the Primate Upper Limb
title_short Spatial and Temporal Arrangement of Recurrent Inhibition in the Primate Upper Limb
title_sort spatial and temporal arrangement of recurrent inhibition in the primate upper limb
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896010/
https://www.ncbi.nlm.nih.gov/pubmed/33334866
http://dx.doi.org/10.1523/JNEUROSCI.1589-20.2020
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