Literature DB >> 6492004

Facilitation of soleus-coupled Renshaw cells during voluntary contraction of pretibial flexor muscles in man.

R Katz, E Pierrot-Deseilligny.   

Abstract

Recurrent inhibition to soleus motoneurones, brought about by a conditioning H-reflex discharge, was estimated in human subjects by a subsequent test H reflex. Changes in recurrent inhibition during voluntary ankle dorsiflexion were evaluated by comparing the amplitude of the test H reflex to a reference H reflex: both reflexes were subjected to the same type of influences which modified soleus monosynaptic reflex excitability during pretibial flexor contraction, but only the test H reflex was subject to the recurrent inhibition evoked by the conditioning H-reflex discharge. During tonic or phasic ramp contractions of the pretibial flexors the inhibition of the test H reflex, as compared to rest, was more marked than that of the reference H reflex. Evidence is presented that this may indicate a facilitation of soleus-coupled Renshaw cells. Since this facilitation of soleus-coupled Renshaw cells was also observed before ramp contraction, it is, at least in part, supraspinal in origin. Within the range of forces studied (8-45% of maximum force) there was no evidence that the facilitation of soleus-coupled Renshaw cells increased along with increased force of the pretibial flexor voluntary contraction. During voluntary phasic ankle dorsiflexion, facilitation of soleus-coupled Renshaw cells was maximum at the moment when soleus motoneurones were most facilitated by the stretch-induced soleus I a discharge. There was no evidence for changes in Renshaw cell excitability during ballistic contractions. It is suggested that this facilitation of soleus-coupled Renshaw cells may be one of the mechanisms preventing the occurrence of a soleus stretch reflex during a voluntary ankle dorsiflexion. Such a mechanism could become important if reciprocal inhibition, via I a inhibitory interneurones, were not strong enough, e.g. because of a weak gamma-drive to the contracting muscles.

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Year:  1984        PMID: 6492004      PMCID: PMC1193512          DOI: 10.1113/jphysiol.1984.sp015440

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  21 in total

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Journal:  J Neurol Neurosurg Psychiatry       Date:  1975-07       Impact factor: 10.154

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Journal:  J Physiol       Date:  1966-07       Impact factor: 5.182

4.  Input-output relations in the pathway of recurrent inhibition to motoneurones in the cat.

Authors:  H Hultborn; E Pierrot-Deseilligny
Journal:  J Physiol       Date:  1979-12       Impact factor: 5.182

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Authors:  E Pierrot-Deseilligny; P Lacert; H P Cathala
Journal:  Physiol Behav       Date:  1971-10

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Authors:  R Tanaka
Journal:  Exp Brain Res       Date:  1974       Impact factor: 1.972

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Authors:  A Prochazka; M Hulliger
Journal:  Adv Neurol       Date:  1983

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Authors:  E Pierrot-Deseilligny; C Bergego; R Katz
Journal:  Brain Res       Date:  1982-02-11       Impact factor: 3.252

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Authors:  E Pierrot-Deseilligny; R Katz; C Morin
Journal:  Brain Res       Date:  1979-04-20       Impact factor: 3.252

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Authors:  H Hultborn; E Pierrot-Deseilligny; H Wigström
Journal:  J Physiol       Date:  1979-12       Impact factor: 5.182

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  8 in total

1.  Modulation of recurrent inhibition from knee extensors to ankle motoneurones during human walking.

Authors:  Jean-Charles Lamy; Caroline Iglesias; Alexandra Lackmy; Jens Bo Nielsen; Rose Katz; Véronique Marchand-Pauvert
Journal:  J Physiol       Date:  2008-10-20       Impact factor: 5.182

2.  Monosynaptic Ia excitation and recurrent inhibition from quadriceps to ankle flexors and extensors in man.

Authors:  S Meunier; A Penicaud; E Pierrot-Deseilligny; A Rossi
Journal:  J Physiol       Date:  1990-04       Impact factor: 5.182

3.  Evidence of facilitation of soleus-coupled Renshaw cells during voluntary co-contraction of antagonistic ankle muscles in man.

Authors:  J Nielsen; E Pierrot-Deseilligny
Journal:  J Physiol       Date:  1996-06-01       Impact factor: 5.182

4.  Inhibitory connections of ipsilateral semicircular canal afferents onto Renshaw cells in the lumbar spinal cord of the cat.

Authors:  H G Ross; M Thewissen
Journal:  J Physiol       Date:  1987-07       Impact factor: 5.182

5.  Reciprocal Ia inhibition between ankle flexors and extensors in man.

Authors:  C Crone; H Hultborn; B Jespersen; J Nielsen
Journal:  J Physiol       Date:  1987-08       Impact factor: 5.182

6.  Depression of Renshaw recurrent inhibition by activation of corticospinal fibres in human upper and lower limb.

Authors:  R Mazzocchio; A Rossi; J C Rothwell
Journal:  J Physiol       Date:  1994-12-01       Impact factor: 5.182

7.  Pattern of heteronymous recurrent inhibition in the human lower limb.

Authors:  S Meunier; E Pierrot-Deseilligny; M Simonetta-Moreau
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

8.  Presence of homonymous recurrent inhibition in motoneurones supplying different lower limb muscles in humans.

Authors:  A Rossi; R Mazzocchio
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

  8 in total

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