Cargando…

The Existence of the StartReact Effect Implies Reticulospinal, Not Corticospinal, Inputs Dominate Drive to Motoneurons during Voluntary Movement

Reaction time is accelerated if a loud (startling) sound accompanies the cue—the “StartReact” effect. Animal studies revealed a reticulospinal substrate for the startle reflex; StartReact may similarly involve the reticulospinal tract, but this is currently uncertain. Here we trained two female maca...

Descripción completa

Detalles Bibliográficos
Autores principales: Tapia, Jesus A., Tohyama, Takamichi, Poll, Annie, Baker, Stuart N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546468/
https://www.ncbi.nlm.nih.gov/pubmed/36658461
http://dx.doi.org/10.1523/JNEUROSCI.2473-21.2022
_version_ 1784805048661835776
author Tapia, Jesus A.
Tohyama, Takamichi
Poll, Annie
Baker, Stuart N.
author_facet Tapia, Jesus A.
Tohyama, Takamichi
Poll, Annie
Baker, Stuart N.
author_sort Tapia, Jesus A.
collection PubMed
description Reaction time is accelerated if a loud (startling) sound accompanies the cue—the “StartReact” effect. Animal studies revealed a reticulospinal substrate for the startle reflex; StartReact may similarly involve the reticulospinal tract, but this is currently uncertain. Here we trained two female macaque monkeys to perform elbow flexion/extension movements following a visual cue. The cue was sometimes accompanied by a loud sound, generating a StartReact effect in electromyogram response latency, as seen in humans. Extracellular recordings were made from antidromically identified corticospinal neurons in primary motor cortex (M1), from the reticular formation (RF), and from the spinal cord (SC; C5–C8 segments). After loud sound, task-related activity was suppressed in M1 (latency, 70–200 ms after cue), but was initially enhanced (70–80 ms) and then suppressed (140–210 ms) in RF. SC activity was unchanged. In a computational model, we simulated a motoneuron pool receiving input from different proportions of the average M1 and RF activity recorded experimentally. Motoneuron firing generated simulated electromyogram, allowing reaction time measurements. Only if ≥60% of motoneuron drive came from RF (≤40% from M1) did loud sound shorten reaction time. The extent of shortening increased as more drive came from RF. If RF provided <60% of drive, loud sound lengthened the reaction time—the opposite of experimental findings. The majority of the drive for voluntary movements is thus likely to originate from the brainstem, not the cortex; changes in the magnitude of the StartReact effect can measure a shift in the relative importance of descending systems. SIGNIFICANCE STATEMENT Our results reveal that a loud sound has opposite effects on neural spiking in corticospinal cells from primary motor cortex, and in the reticular formation. We show that this fortuitously allows changes in reaction time produced by a loud sound to be used to assess the relative importance of reticulospinal versus corticospinal control of movement, validating previous noninvasive measurements in humans. Our findings suggest that the majority of the descending drive to motoneurons producing voluntary movement in primates comes from the reticulospinal tract, not the corticospinal tract.
format Online
Article
Text
id pubmed-9546468
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Society for Neuroscience
record_format MEDLINE/PubMed
spelling pubmed-95464682022-10-11 The Existence of the StartReact Effect Implies Reticulospinal, Not Corticospinal, Inputs Dominate Drive to Motoneurons during Voluntary Movement Tapia, Jesus A. Tohyama, Takamichi Poll, Annie Baker, Stuart N. J Neurosci Research Articles Reaction time is accelerated if a loud (startling) sound accompanies the cue—the “StartReact” effect. Animal studies revealed a reticulospinal substrate for the startle reflex; StartReact may similarly involve the reticulospinal tract, but this is currently uncertain. Here we trained two female macaque monkeys to perform elbow flexion/extension movements following a visual cue. The cue was sometimes accompanied by a loud sound, generating a StartReact effect in electromyogram response latency, as seen in humans. Extracellular recordings were made from antidromically identified corticospinal neurons in primary motor cortex (M1), from the reticular formation (RF), and from the spinal cord (SC; C5–C8 segments). After loud sound, task-related activity was suppressed in M1 (latency, 70–200 ms after cue), but was initially enhanced (70–80 ms) and then suppressed (140–210 ms) in RF. SC activity was unchanged. In a computational model, we simulated a motoneuron pool receiving input from different proportions of the average M1 and RF activity recorded experimentally. Motoneuron firing generated simulated electromyogram, allowing reaction time measurements. Only if ≥60% of motoneuron drive came from RF (≤40% from M1) did loud sound shorten reaction time. The extent of shortening increased as more drive came from RF. If RF provided <60% of drive, loud sound lengthened the reaction time—the opposite of experimental findings. The majority of the drive for voluntary movements is thus likely to originate from the brainstem, not the cortex; changes in the magnitude of the StartReact effect can measure a shift in the relative importance of descending systems. SIGNIFICANCE STATEMENT Our results reveal that a loud sound has opposite effects on neural spiking in corticospinal cells from primary motor cortex, and in the reticular formation. We show that this fortuitously allows changes in reaction time produced by a loud sound to be used to assess the relative importance of reticulospinal versus corticospinal control of movement, validating previous noninvasive measurements in humans. Our findings suggest that the majority of the descending drive to motoneurons producing voluntary movement in primates comes from the reticulospinal tract, not the corticospinal tract. Society for Neuroscience 2022-10-05 /pmc/articles/PMC9546468/ /pubmed/36658461 http://dx.doi.org/10.1523/JNEUROSCI.2473-21.2022 Text en Copyright © 2022 Tapia, Tohyama 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
Tapia, Jesus A.
Tohyama, Takamichi
Poll, Annie
Baker, Stuart N.
The Existence of the StartReact Effect Implies Reticulospinal, Not Corticospinal, Inputs Dominate Drive to Motoneurons during Voluntary Movement
title The Existence of the StartReact Effect Implies Reticulospinal, Not Corticospinal, Inputs Dominate Drive to Motoneurons during Voluntary Movement
title_full The Existence of the StartReact Effect Implies Reticulospinal, Not Corticospinal, Inputs Dominate Drive to Motoneurons during Voluntary Movement
title_fullStr The Existence of the StartReact Effect Implies Reticulospinal, Not Corticospinal, Inputs Dominate Drive to Motoneurons during Voluntary Movement
title_full_unstemmed The Existence of the StartReact Effect Implies Reticulospinal, Not Corticospinal, Inputs Dominate Drive to Motoneurons during Voluntary Movement
title_short The Existence of the StartReact Effect Implies Reticulospinal, Not Corticospinal, Inputs Dominate Drive to Motoneurons during Voluntary Movement
title_sort existence of the startreact effect implies reticulospinal, not corticospinal, inputs dominate drive to motoneurons during voluntary movement
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546468/
https://www.ncbi.nlm.nih.gov/pubmed/36658461
http://dx.doi.org/10.1523/JNEUROSCI.2473-21.2022
work_keys_str_mv AT tapiajesusa theexistenceofthestartreacteffectimpliesreticulospinalnotcorticospinalinputsdominatedrivetomotoneuronsduringvoluntarymovement
AT tohyamatakamichi theexistenceofthestartreacteffectimpliesreticulospinalnotcorticospinalinputsdominatedrivetomotoneuronsduringvoluntarymovement
AT pollannie theexistenceofthestartreacteffectimpliesreticulospinalnotcorticospinalinputsdominatedrivetomotoneuronsduringvoluntarymovement
AT bakerstuartn theexistenceofthestartreacteffectimpliesreticulospinalnotcorticospinalinputsdominatedrivetomotoneuronsduringvoluntarymovement
AT tapiajesusa existenceofthestartreacteffectimpliesreticulospinalnotcorticospinalinputsdominatedrivetomotoneuronsduringvoluntarymovement
AT tohyamatakamichi existenceofthestartreacteffectimpliesreticulospinalnotcorticospinalinputsdominatedrivetomotoneuronsduringvoluntarymovement
AT pollannie existenceofthestartreacteffectimpliesreticulospinalnotcorticospinalinputsdominatedrivetomotoneuronsduringvoluntarymovement
AT bakerstuartn existenceofthestartreacteffectimpliesreticulospinalnotcorticospinalinputsdominatedrivetomotoneuronsduringvoluntarymovement