Literature DB >> 9821627

Evaluation of reciprocal inhibition of the soleus H-reflex during tonic plantar flexion in man.

N Petersen1, H Morita, J Nielsen.   

Abstract

Changes in reciprocal inhibition from ankle dorsiflexors to ankle plantar flexors were evaluated at increasing levels of tonic plantar flexion in 11 healthy subjects. Stimulation of the common peroneal nerve (CPN) evoked a short-latency depression of the rectified and averaged soleus electromyogram (average latency of depression: 40 ms) and a short-latency inhibition of the soleus H-reflex (conditioning-test interval: 2-3 ms). When the intensity of the CPN stimulation was below approximately 1.2 x motor threshold (x MT) the inhibition of both the soleus EMG (expressed as the amount of EMG during the inhibition as percentage of the background EMG) and the soleus H-reflex (expressed as the size of the conditioned reflex as percentage of the control H-reflex size) were seen to decrease with increasing levels of plantar flexion. At intensities of stimulation higher than approximately 1.2 x MT the inhibition of the EMG and the H-reflex was very strong and was not modulated with contraction. It is suggested that the decrease of reciprocal inhibition with increasing levels of plantar flexion is due to a decreased excitability of the Ia inhibitory interneurones which are responsible for the inhibition. It is emphasized that submaximal stimulation is necessary to demonstrate this modulation of inhibition and that the functional contribution of reciprocal inhibition to motor performance cannot be revealed from the amount of inhibition evoked by artificial electrical stimulation of a peripheral nerve.

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Mesh:

Year:  1998        PMID: 9821627     DOI: 10.1016/s0165-0270(98)00044-2

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


  18 in total

1.  Suppression of soleus H-reflex amplitude is graded with frequency of rhythmic arm cycling.

Authors:  Sandra R Hundza; E Paul Zehr
Journal:  Exp Brain Res       Date:  2008-11-15       Impact factor: 1.972

2.  Rhythmic arm cycling differentially modulates stretch and H-reflex amplitudes in soleus muscle.

Authors:  Andres F Palomino; Sandra R Hundza; E Paul Zehr
Journal:  Exp Brain Res       Date:  2011-09-08       Impact factor: 1.972

3.  Facilitation from flexor digitorum superficialis to extensor carpi radialis in humans.

Authors:  Mitsuhiro Nito; Wataru Hashizume; Takuji Miyasaka; Katsuhiko Suzuki; Toshiaki Sato; Hiromi Fujii; Masaomi Shindo; Akira Naito
Journal:  Exp Brain Res       Date:  2016-03-24       Impact factor: 1.972

4.  Reciprocal inhibition post-stroke is related to reflex excitability and movement ability.

Authors:  Neha Bhagchandani; Sheila Schindler-Ivens
Journal:  Clin Neurophysiol       Date:  2012-05-19       Impact factor: 3.708

5.  Short-term plasticity of human spinal inhibitory circuits after isometric and isotonic ankle training.

Authors:  Traci Jessop; Alyssa DePaola; Lauren Casaletto; Chaya Englard; Maria Knikou
Journal:  Eur J Appl Physiol       Date:  2012-06-09       Impact factor: 3.078

6.  Oligosynaptic inhibition mediated by group Ia afferents from flexor digitorum superficialis to wrist flexors in humans.

Authors:  Mitsuhiro Nito; Wataru Hashizume; Manabu Jimenji; Katsuhiko Suzuki; Toshiaki Sato; Hiromi Fujii; Takuji Miyasaka; Masaomi Shindo; Akira Naito
Journal:  Exp Brain Res       Date:  2018-04-20       Impact factor: 1.972

7.  Modulation of reciprocal inhibition between ankle extensors and flexors during walking in man.

Authors:  N Petersen; H Morita; J Nielsen
Journal:  J Physiol       Date:  1999-10-15       Impact factor: 5.182

8.  Convergence of ipsi- and contralateral muscle afferents on common interneurons mediating reciprocal inhibition of ankle plantarflexors in humans.

Authors:  Natalie Mrachacz-Kersting; S S Geertsen; A J T Stevenson; J B Nielsen
Journal:  Exp Brain Res       Date:  2017-03-03       Impact factor: 1.972

9.  Reduced reciprocal inhibition is seen only in spastic limbs in patients with neurolathyrism.

Authors:  C Crone; N T Petersen; S Gimenéz-Roldán; B Lungholt; K Nyborg; J B Nielsen
Journal:  Exp Brain Res       Date:  2007-06-15       Impact factor: 1.972

10.  Immobilization induces changes in presynaptic control of group Ia afferents in healthy humans.

Authors:  Jesper Lundbye-Jensen; Jens Bo Nielsen
Journal:  J Physiol       Date:  2008-07-03       Impact factor: 5.182

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