Excitability of reciprocal and recurrent inhibitory pathways after voluntary muscle relaxation in man
- PMID: 4029300
- DOI: 10.1007/BF00230904
Excitability of reciprocal and recurrent inhibitory pathways after voluntary muscle relaxation in man
Abstract
We studied the potential contribution of postsynaptic mechanisms to the depression of reflex excitability which occurs immediately after a voluntary release from tonic muscle contraction. The excitability of the Soleus (Sol) motor pool was tested at rest and after voluntary muscle relaxation. In both cases the Sol H-reflex was conditioned by a single shock to the peroneal nerve, in order to activate the Ia interneurones (INs) mediating the reciprocal inhibition via a peripheral input, or by a short-lasting voluntary contraction of the Tibialis Anterior (TA) muscle, to activate the Ia INs via a central command. Changes in excitability of Renshaw cells were also tested at rest and after release, to assess the role of recurrent inhibition in the release-induced inhibition of the Sol H-reflex. It was demonstrated that: the excitability of the INs mediating the reciprocal inhibition was only slightly enhanced in comparison with resting conditions; the H-reflex of the antagonist muscle (TA) evoked after Sol release was not consistently facilitated with respect to rest; the command to contract the TA muscle reduced the H-reflex of the Sol muscle during rest but not after Sol release; recurrent inhibition did not increase its effect in the post-release period. Such features suggest that recurrent and reciprocal post-synaptic inhibitions do not play a major role in reducing the reflex excitability of a relaxing muscle; rather, the command to release prevents the reciprocal inhibitory effect which accompanies the contraction of the antagonist muscle.(ABSTRACT TRUNCATED AT 250 WORDS)
Similar articles
-
Reciprocal Ia inhibition between ankle flexors and extensors in man.J Physiol. 1987 Aug;389:163-85. doi: 10.1113/jphysiol.1987.sp016652. J Physiol. 1987. PMID: 3681725 Free PMC article.
-
Facilitation of soleus-coupled Renshaw cells during voluntary contraction of pretibial flexor muscles in man.J Physiol. 1984 Oct;355:587-603. doi: 10.1113/jphysiol.1984.sp015440. J Physiol. 1984. PMID: 6492004 Free PMC article.
-
Changes in recurrent inhibition during voluntary soleus contractions in man studied by an H-reflex technique.J Physiol. 1979 Dec;297(0):229-51. doi: 10.1113/jphysiol.1979.sp013037. J Physiol. 1979. PMID: 536912 Free PMC article.
-
Reciprocal inhibition in man.Dan Med Bull. 1993 Nov;40(5):571-81. Dan Med Bull. 1993. PMID: 8299401 Review.
-
Electromyography in disorders of muscle tone.Can J Neurol Sci. 1987 Aug;14(3 Suppl):501-5. doi: 10.1017/s0317167100037999. Can J Neurol Sci. 1987. PMID: 3315152 Review.
Cited by
-
The effect of initiation prediction and non-prediction on muscle relaxation control.J Phys Ther Sci. 2023 Apr;35(4):293-299. doi: 10.1589/jpts.35.293. Epub 2023 Apr 1. J Phys Ther Sci. 2023. PMID: 37020829 Free PMC article.
-
Reflex excitability of human soleus motoneurones during voluntary shortening or lengthening contractions.J Physiol. 1987 Sep;390:271-84. doi: 10.1113/jphysiol.1987.sp016699. J Physiol. 1987. PMID: 3443936 Free PMC article.
-
Excitability of the soleus H-reflex arc during walking and stepping in man.Exp Brain Res. 1987;66(1):49-60. doi: 10.1007/BF00236201. Exp Brain Res. 1987. PMID: 3582535
-
Time Course of Corticospinal Excitability and Intracortical Inhibition Just before Muscle Relaxation.Front Hum Neurosci. 2016 Jan 28;10:1. doi: 10.3389/fnhum.2016.00001. eCollection 2016. Front Hum Neurosci. 2016. PMID: 26858619 Free PMC article.
-
Muscle stretching and motoneuron excitability.Eur J Appl Physiol Occup Physiol. 1988;58(1-2):47-52. doi: 10.1007/BF00636602. Eur J Appl Physiol Occup Physiol. 1988. PMID: 3203674