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Cortical output to fast and slow muscles of the ankle in the rhesus macaque

The cortical control of fast and slow muscles of the ankle has been the subject of numerous reports yielding conflicting results. Although it is generally agreed that cortical stimulation yields short latency facilitation of fast muscles, the effects on the slow muscle, soleus, remain controversial....

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Autores principales: Hudson, Heather M., Griffin, Darcy M., Belhaj-Saïf, Abderraouf, Cheney, Paul D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585439/
https://www.ncbi.nlm.nih.gov/pubmed/23459919
http://dx.doi.org/10.3389/fncir.2013.00033
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author Hudson, Heather M.
Griffin, Darcy M.
Belhaj-Saïf, Abderraouf
Cheney, Paul D.
author_facet Hudson, Heather M.
Griffin, Darcy M.
Belhaj-Saïf, Abderraouf
Cheney, Paul D.
author_sort Hudson, Heather M.
collection PubMed
description The cortical control of fast and slow muscles of the ankle has been the subject of numerous reports yielding conflicting results. Although it is generally agreed that cortical stimulation yields short latency facilitation of fast muscles, the effects on the slow muscle, soleus, remain controversial. Some studies have shown predominant facilitation of soleus from the cortex while others have provided evidence of differential control in which soleus is predominantly inhibited from the cortex. The objective of this study was to investigate the cortical control of fast and slow muscles of the ankle using stimulus triggered averaging (StTA) of EMG activity, which is a sensitive method of detecting output effects on muscle activity. This method also has relatively high spatial resolution and can be applied in awake, behaving subjects. Two rhesus macaques were trained to perform a hindlimb push-pull task. Stimulus triggered averages (StTAs) of EMG activity (15, 30, and 60 μA at 15 Hz) were computed for four muscles of the ankle [tibialis anterior (TA), medial gastrocnemius (MG), lateral gastrocnemius (LG), and soleus] as the monkeys performed the task. Poststimulus facilitation (PStF) was observed in both the fast muscles (TA, MG, and LG) as well as the slow muscle (soleus) and was as common and as strong in soleus as in the fast muscles. However, while poststimulus suppression (PStS) was observed in all muscles, it was more common in the slow muscle compared to the fast muscles and was as common as facilitation at low stimulus intensities. Overall, our results demonstrate that cortical facilitation of soleus has an organization that is very similar to that of the fast ankle muscles. However, cortical inhibition is organized differently allowing for more prominent suppression of soleus motoneurons.
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spelling pubmed-35854392013-03-04 Cortical output to fast and slow muscles of the ankle in the rhesus macaque Hudson, Heather M. Griffin, Darcy M. Belhaj-Saïf, Abderraouf Cheney, Paul D. Front Neural Circuits Neuroscience The cortical control of fast and slow muscles of the ankle has been the subject of numerous reports yielding conflicting results. Although it is generally agreed that cortical stimulation yields short latency facilitation of fast muscles, the effects on the slow muscle, soleus, remain controversial. Some studies have shown predominant facilitation of soleus from the cortex while others have provided evidence of differential control in which soleus is predominantly inhibited from the cortex. The objective of this study was to investigate the cortical control of fast and slow muscles of the ankle using stimulus triggered averaging (StTA) of EMG activity, which is a sensitive method of detecting output effects on muscle activity. This method also has relatively high spatial resolution and can be applied in awake, behaving subjects. Two rhesus macaques were trained to perform a hindlimb push-pull task. Stimulus triggered averages (StTAs) of EMG activity (15, 30, and 60 μA at 15 Hz) were computed for four muscles of the ankle [tibialis anterior (TA), medial gastrocnemius (MG), lateral gastrocnemius (LG), and soleus] as the monkeys performed the task. Poststimulus facilitation (PStF) was observed in both the fast muscles (TA, MG, and LG) as well as the slow muscle (soleus) and was as common and as strong in soleus as in the fast muscles. However, while poststimulus suppression (PStS) was observed in all muscles, it was more common in the slow muscle compared to the fast muscles and was as common as facilitation at low stimulus intensities. Overall, our results demonstrate that cortical facilitation of soleus has an organization that is very similar to that of the fast ankle muscles. However, cortical inhibition is organized differently allowing for more prominent suppression of soleus motoneurons. Frontiers Media S.A. 2013-03-01 /pmc/articles/PMC3585439/ /pubmed/23459919 http://dx.doi.org/10.3389/fncir.2013.00033 Text en Copyright © 2013 Hudson, Griffin, Belhaj-Saïf and Cheney. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Hudson, Heather M.
Griffin, Darcy M.
Belhaj-Saïf, Abderraouf
Cheney, Paul D.
Cortical output to fast and slow muscles of the ankle in the rhesus macaque
title Cortical output to fast and slow muscles of the ankle in the rhesus macaque
title_full Cortical output to fast and slow muscles of the ankle in the rhesus macaque
title_fullStr Cortical output to fast and slow muscles of the ankle in the rhesus macaque
title_full_unstemmed Cortical output to fast and slow muscles of the ankle in the rhesus macaque
title_short Cortical output to fast and slow muscles of the ankle in the rhesus macaque
title_sort cortical output to fast and slow muscles of the ankle in the rhesus macaque
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585439/
https://www.ncbi.nlm.nih.gov/pubmed/23459919
http://dx.doi.org/10.3389/fncir.2013.00033
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