Effects of postural and voluntary muscle contraction on modulation of the soleus H reflex by transcranial magnetic stimulation

Modulation of spinal reflexes depends largely on the integrity of the corticospinal tract. A useful method to document the influence of descending tracts on reflexes is to examine the effects of transcranial magnetic stimulation (TMS) on the soleus H reflex elicited by posterior tibial nerve electri...

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Veröffentlicht in:Experimental brain research 2015-12, Vol.233 (12), p.3425-3431
Hauptverfasser: Guzmán-López, Jessica, Selvi, Aikaterini, Solà-Valls, Núria, Casanova-Molla, Jordi, Valls-Solé, Josep
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Sprache:eng
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Zusammenfassung:Modulation of spinal reflexes depends largely on the integrity of the corticospinal tract. A useful method to document the influence of descending tracts on reflexes is to examine the effects of transcranial magnetic stimulation (TMS) on the soleus H reflex elicited by posterior tibial nerve electrical stimuli (PTS). In 12 healthy volunteers, we investigated how postural or voluntary muscle contraction modified such descending modulation. We first characterized the effects of TMS at 95 % of motor threshold for leg responses on the H reflex elicited by a preceding PTS at inter-stimuli intervals (ISIs) between 0 and 120 ms at rest and, then, during voluntary plantar flexion (pf), dorsal flexion (df), and standing still (ss). During pf, there was an increase in the facilitation of the H reflex at ISIs 0–20 ms. During df, there were no effects of TMS on the H reflex. During ss, there was inhibition at ISIs 40–60 ms. Our observations suggest that muscle contraction prevails over the baseline effects of TMS on the soleus H reflex. While contraction of the antagonist (df) suppressed most of the effects, contraction of the agonist had different effects depending on the type of activity (pf or ss). The characterization of the interaction between descending corticospinal volleys and segmental peripheral inputs provides useful information on motor control for physiological research and further understanding of the effects of spinal cord lesions.
ISSN:0014-4819
1432-1106
DOI:10.1007/s00221-015-4417-3