Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1984 Oct;355:587–603. doi: 10.1113/jphysiol.1984.sp015440

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

R Katz, E Pierrot-Deseilligny
PMCID: PMC1193512  PMID: 6492004

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.

Full text

PDF

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bussel B., Pierrot-Deseilligny E. Inhibition of human motoneurons, probably of Renshaw origin, elicited by an orthodromic motor discharge. J Physiol. 1977 Jul;269(2):319–339. doi: 10.1113/jphysiol.1977.sp011904. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Devanandan M. S., Eccles R. M., Stenhouse D. Presynaptic inhibition evoked by muscle contraction. J Physiol. 1966 Jul;185(2):471–485. doi: 10.1113/jphysiol.1966.sp007997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Gottlieb G. L., Agarwal G. C., Stark L. Interactions between voluntary and postural mechanisms of thehuman motor system. J Neurophysiol. 1970 May;33(3):365–381. doi: 10.1152/jn.1970.33.3.365. [DOI] [PubMed] [Google Scholar]
  4. Hagbarth K. E., Wallen G., Löfstedt L. Muscle spindle activity in man during voluntary fast alternating movements. J Neurol Neurosurg Psychiatry. 1975 Jul;38(7):625–635. doi: 10.1136/jnnp.38.7.625. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hultborn H., Pierrot-Deseilligny E. Changes in recurrent inhibition during voluntary soleus contractions in man studied by an H-reflex technique. J Physiol. 1979 Dec;297(0):229–251. doi: 10.1113/jphysiol.1979.sp013037. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hultborn H., Pierrot-Deseilligny E. Input-output relations in the pathway of recurrent inhibition to motoneurones in the cat. J Physiol. 1979 Dec;297(0):267–287. doi: 10.1113/jphysiol.1979.sp013039. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hultborn H., Pierrot-Deseilligny E., Wigström H. Recurrent inhibition and afterhyperpolarization following motoneuronal discharge in the cat. J Physiol. 1979 Dec;297(0):253–266. doi: 10.1113/jphysiol.1979.sp013038. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Katz R., Pierrot-Deseilligny E. Recurrent inhibition of alpha-motoneurons in patients with upper motor neuron lesions. Brain. 1982 Mar;105(Pt 1):103–124. doi: 10.1093/brain/105.1.103. [DOI] [PubMed] [Google Scholar]
  9. Morin C., Pierrot-Deseilligny E., Hultborn H. Evidence for presynaptic inhibition of muscle spindle Ia afferents in man. Neurosci Lett. 1984 Feb 10;44(2):137–142. doi: 10.1016/0304-3940(84)90071-5. [DOI] [PubMed] [Google Scholar]
  10. Morin C., Pierrot-Deseilligny E. Role of Ia afferents in the soleus motoneurones. Inhibition during a tibialis anterior voluntary contraction in man. Exp Brain Res. 1977 Apr 21;27(5):509–522. doi: 10.1007/BF00239040. [DOI] [PubMed] [Google Scholar]
  11. Piercey M. F., Goldfarb J. Discharge patterns of Renshaw cells evoked by volleys in ipsilateral cutaneous and high-threshold muscle afferents and their relationship to reflexes recorded in ventral roots. J Neurophysiol. 1974 Mar;37(2):294–302. doi: 10.1152/jn.1974.37.2.294. [DOI] [PubMed] [Google Scholar]
  12. Pierrot-Deseilligny E., Bergego C., Katz R. Reversal in cutaneous of Ib pathways during human voluntary contraction. Brain Res. 1982 Feb 11;233(2):400–403. doi: 10.1016/0006-8993(82)91213-6. [DOI] [PubMed] [Google Scholar]
  13. Pierrot-Deseilligny E., Katz R., Morin C. Evidence of Ib inhibition in human subjects. Brain Res. 1979 Apr 20;166(1):176–179. doi: 10.1016/0006-8993(79)90660-7. [DOI] [PubMed] [Google Scholar]
  14. Pierrot-Deseilligny E., Lacert P., Cathala H. P. Amplitude et variabilité des réflexes monosynaptiques avant un mouvement volontaire. Physiol Behav. 1971 Oct;7(4):495–508. doi: 10.1016/0031-9384(71)90100-4. [DOI] [PubMed] [Google Scholar]
  15. Pierrot-Deseilligny E., Morin C., Bergego C., Tankov N. Pattern of group I fibre projections from ankle flexor and extensor muscles in man. Exp Brain Res. 1981;42(3-4):337–350. doi: 10.1007/BF00237499. [DOI] [PubMed] [Google Scholar]
  16. Pierrot-Deseilligny E., Morin C., Katz R., Bussel B. Influence of voluntary movement and posture on recurrent inhibition in human subjects. Brain Res. 1977 Apr 1;124(3):427–436. doi: 10.1016/0006-8993(77)90944-1. [DOI] [PubMed] [Google Scholar]
  17. Prochazka A., Hulliger M. Muscle afferent function and its significance for motor control mechanisms during voluntary movements in cat, monkey, and man. Adv Neurol. 1983;39:93–132. [PubMed] [Google Scholar]
  18. Ryall R. W. Renshaw cell mediated inhibition of Renshaw cells: patterns of excitation and inhibition from impulses in motor axon collaterals. J Neurophysiol. 1970 Mar;33(2):257–270. doi: 10.1152/jn.1970.33.2.257. [DOI] [PubMed] [Google Scholar]
  19. Simoyama M., Tanaka R. Reciprocal La inhibition at the onset of voluntary movements in man. Brain Res. 1974 Dec 27;82(2):334–337. doi: 10.1016/0006-8993(74)90615-5. [DOI] [PubMed] [Google Scholar]
  20. Tanaka R. Reciprocal Ia inhibition during voluntary movements in man. Exp Brain Res. 1974;21(5):529–540. doi: 10.1007/BF00237171. [DOI] [PubMed] [Google Scholar]
  21. Vallbo A. B., Hagbarth K. E., Torebjörk H. E., Wallin B. G. Somatosensory, proprioceptive, and sympathetic activity in human peripheral nerves. Physiol Rev. 1979 Oct;59(4):919–957. doi: 10.1152/physrev.1979.59.4.919. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES