Neural mechanisms influencing interlimb coordination during locomotion in humans: presynaptic modulation of forearm H-reflexes during leg cycling.

Presynaptic inhibition of transmission between Ia afferent terminals and alpha motoneurons (Ia PSI) is a major control mechanism associated with soleus H-reflex modulation during human locomotion. Rhythmic arm cycling suppresses soleus H-reflex amplitude by increasing segmental Ia PSI. There is a re...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Tsuyoshi Nakajima, Rinaldo A Mezzarane, Taryn Klarner, Trevor S Barss, Sandra R Hundza, Tomoyoshi Komiyama, E Paul Zehr
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
Materias:
R
Q
Acceso en línea:https://doaj.org/article/69d1db76b89d466f934ff4d3ab872db6
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:69d1db76b89d466f934ff4d3ab872db6
record_format dspace
spelling oai:doaj.org-article:69d1db76b89d466f934ff4d3ab872db62021-11-18T08:50:28ZNeural mechanisms influencing interlimb coordination during locomotion in humans: presynaptic modulation of forearm H-reflexes during leg cycling.1932-620310.1371/journal.pone.0076313https://doaj.org/article/69d1db76b89d466f934ff4d3ab872db62013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24204611/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Presynaptic inhibition of transmission between Ia afferent terminals and alpha motoneurons (Ia PSI) is a major control mechanism associated with soleus H-reflex modulation during human locomotion. Rhythmic arm cycling suppresses soleus H-reflex amplitude by increasing segmental Ia PSI. There is a reciprocal organization in the human nervous system such that arm cycling modulates H-reflexes in leg muscles and leg cycling modulates H-reflexes in forearm muscles. However, comparatively little is known about mechanisms subserving the effects from leg to arm. Using a conditioning-test (C-T) stimulation paradigm, the purpose of this study was to test the hypothesis that changes in Ia PSI underlie the modulation of H-reflexes in forearm flexor muscles during leg cycling. Subjects performed leg cycling and static activation while H-reflexes were evoked in forearm flexor muscles. H-reflexes were conditioned with either electrical stimuli to the radial nerve (to increase Ia PSI; C-T interval  = 20 ms) or to the superficial radial (SR) nerve (to reduce Ia PSI; C-T interval  = 37-47 ms). While stationary, H-reflex amplitudes were significantly suppressed by radial nerve conditioning and facilitated by SR nerve conditioning. Leg cycling suppressed H-reflex amplitudes and the amount of this suppression was increased with radial nerve conditioning. SR conditioning stimulation removed the suppression of H-reflex amplitude resulting from leg cycling. Interestingly, these effects and interactions on H-reflex amplitudes were observed with subthreshold conditioning stimulus intensities (radial n., ∼0.6×MT; SR n., ∼ perceptual threshold) that did not have clear post synaptic effects. That is, did not evoke reflexes in the surface EMG of forearm flexor muscles. We conclude that the interaction between leg cycling and somatosensory conditioning of forearm H-reflex amplitudes is mediated by modulation of Ia PSI pathways. Overall our results support a conservation of neural control mechanisms between the arms and legs during locomotor behaviors in humans.Tsuyoshi NakajimaRinaldo A MezzaraneTaryn KlarnerTrevor S BarssSandra R HundzaTomoyoshi KomiyamaE Paul ZehrPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 10, p e76313 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Tsuyoshi Nakajima
Rinaldo A Mezzarane
Taryn Klarner
Trevor S Barss
Sandra R Hundza
Tomoyoshi Komiyama
E Paul Zehr
Neural mechanisms influencing interlimb coordination during locomotion in humans: presynaptic modulation of forearm H-reflexes during leg cycling.
description Presynaptic inhibition of transmission between Ia afferent terminals and alpha motoneurons (Ia PSI) is a major control mechanism associated with soleus H-reflex modulation during human locomotion. Rhythmic arm cycling suppresses soleus H-reflex amplitude by increasing segmental Ia PSI. There is a reciprocal organization in the human nervous system such that arm cycling modulates H-reflexes in leg muscles and leg cycling modulates H-reflexes in forearm muscles. However, comparatively little is known about mechanisms subserving the effects from leg to arm. Using a conditioning-test (C-T) stimulation paradigm, the purpose of this study was to test the hypothesis that changes in Ia PSI underlie the modulation of H-reflexes in forearm flexor muscles during leg cycling. Subjects performed leg cycling and static activation while H-reflexes were evoked in forearm flexor muscles. H-reflexes were conditioned with either electrical stimuli to the radial nerve (to increase Ia PSI; C-T interval  = 20 ms) or to the superficial radial (SR) nerve (to reduce Ia PSI; C-T interval  = 37-47 ms). While stationary, H-reflex amplitudes were significantly suppressed by radial nerve conditioning and facilitated by SR nerve conditioning. Leg cycling suppressed H-reflex amplitudes and the amount of this suppression was increased with radial nerve conditioning. SR conditioning stimulation removed the suppression of H-reflex amplitude resulting from leg cycling. Interestingly, these effects and interactions on H-reflex amplitudes were observed with subthreshold conditioning stimulus intensities (radial n., ∼0.6×MT; SR n., ∼ perceptual threshold) that did not have clear post synaptic effects. That is, did not evoke reflexes in the surface EMG of forearm flexor muscles. We conclude that the interaction between leg cycling and somatosensory conditioning of forearm H-reflex amplitudes is mediated by modulation of Ia PSI pathways. Overall our results support a conservation of neural control mechanisms between the arms and legs during locomotor behaviors in humans.
format article
author Tsuyoshi Nakajima
Rinaldo A Mezzarane
Taryn Klarner
Trevor S Barss
Sandra R Hundza
Tomoyoshi Komiyama
E Paul Zehr
author_facet Tsuyoshi Nakajima
Rinaldo A Mezzarane
Taryn Klarner
Trevor S Barss
Sandra R Hundza
Tomoyoshi Komiyama
E Paul Zehr
author_sort Tsuyoshi Nakajima
title Neural mechanisms influencing interlimb coordination during locomotion in humans: presynaptic modulation of forearm H-reflexes during leg cycling.
title_short Neural mechanisms influencing interlimb coordination during locomotion in humans: presynaptic modulation of forearm H-reflexes during leg cycling.
title_full Neural mechanisms influencing interlimb coordination during locomotion in humans: presynaptic modulation of forearm H-reflexes during leg cycling.
title_fullStr Neural mechanisms influencing interlimb coordination during locomotion in humans: presynaptic modulation of forearm H-reflexes during leg cycling.
title_full_unstemmed Neural mechanisms influencing interlimb coordination during locomotion in humans: presynaptic modulation of forearm H-reflexes during leg cycling.
title_sort neural mechanisms influencing interlimb coordination during locomotion in humans: presynaptic modulation of forearm h-reflexes during leg cycling.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/69d1db76b89d466f934ff4d3ab872db6
work_keys_str_mv AT tsuyoshinakajima neuralmechanismsinfluencinginterlimbcoordinationduringlocomotioninhumanspresynapticmodulationofforearmhreflexesduringlegcycling
AT rinaldoamezzarane neuralmechanismsinfluencinginterlimbcoordinationduringlocomotioninhumanspresynapticmodulationofforearmhreflexesduringlegcycling
AT tarynklarner neuralmechanismsinfluencinginterlimbcoordinationduringlocomotioninhumanspresynapticmodulationofforearmhreflexesduringlegcycling
AT trevorsbarss neuralmechanismsinfluencinginterlimbcoordinationduringlocomotioninhumanspresynapticmodulationofforearmhreflexesduringlegcycling
AT sandrarhundza neuralmechanismsinfluencinginterlimbcoordinationduringlocomotioninhumanspresynapticmodulationofforearmhreflexesduringlegcycling
AT tomoyoshikomiyama neuralmechanismsinfluencinginterlimbcoordinationduringlocomotioninhumanspresynapticmodulationofforearmhreflexesduringlegcycling
AT epaulzehr neuralmechanismsinfluencinginterlimbcoordinationduringlocomotioninhumanspresynapticmodulationofforearmhreflexesduringlegcycling
_version_ 1718421266947375104