Reciprocal changes of excitability between tibialis anterior and soleus during the sit-to-stand movement

Citation
F. Goulart et J. Valls-sole, Reciprocal changes of excitability between tibialis anterior and soleus during the sit-to-stand movement, EXP BRAIN R, 139(4), 2001, pp. 391-397
Citations number
51
Categorie Soggetti
Neurosciences & Behavoir
Journal title
EXPERIMENTAL BRAIN RESEARCH
ISSN journal
00144819 → ACNP
Volume
139
Issue
4
Year of publication
2001
Pages
391 - 397
Database
ISI
SICI code
0014-4819(200108)139:4<391:RCOEBT>2.0.ZU;2-4
Abstract
The excitability of spinal motoneurons is modified by central preparatory c ommands before muscle activation. In relatively complex long duration motor tasks such as the sit-to-stand (STS) movement, the central nervous system commands have to take into account the inputs from muscle, skin, and joint afferents during muscle contraction. We have investigated the changes occur ring in tibialis anterior (TA) and soleus (SOL) motoneuronal excitability p rior to and during the STS movement in normal subjects. Twelve healthy volu nteers received the instruction to rise from a chair at the perception of a n acoustic 'go' signal. Cortical transcranial magnetic stimuli (TMS) or per ipheral nerve electrical stimuli (PNS) were used as test stimuli to elicit, respectively, the motor evoked potential (MEP) and the H reflex, at interv als of 50-1500 ms after the 'go' signal. Both the MEP and the H reflex were enhanced in the TA between 100 and 900 ms after the 'go' signal. At the sa me time there was inhibition of the H reflex but not of the MEP in the SOL. At the end of the STS movement, during quiet standing, the size of both th e H reflex and the MEP of the TA were not different from those obtained in the sitting position. However, in SOL, the H reflex was smaller, and the ME P was larger, than at rest. Our observations suggest the participation of s everal mechanisms of control of motoneuronal excitability during the STS, u ltimately leading to a dominant role of presynaptic inhibitory mechanisms i n SOL during standing.