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Motor imagery practice during arm-immobilization benefits sensorimotor cortical functions and plasticity-related sleep features

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ABSTRACT Motor imagery (MI) is known to engage motor networks and could compensate for the maladaptive neuroplasticity elicited by immobilization. This hypothesis and associated underlying neural mechanisms remain underexplored. Here, we investigated how MI practice during 11 h of arm-immobilization influences sensorimotor and cortical representations of the hands, as well as sleep. Fourteen participants were first tested after a normal day, followed by two 11-h periods of immobilization, either with concomitant MI treatment or control tasks. Data revealed that MI prevented the consequences of immobilization: (i) alteration of the sensorimotor representation of hands, (ii) decrease of cortical excitability over the primary motor cortex (M1) contralateral to arm-immobilization, and (iii) reduction of sleep spindles over both M1s. Furthermore, (iv) the time spent in REM sleep was significantly longer after MI. These results support that implementing MI during immobilization can limit the deleterious effects of limb disuse, at several levels of sensorimotor functioning.
Title: Motor imagery practice during arm-immobilization benefits sensorimotor cortical functions and plasticity-related sleep features
Description:
ABSTRACT Motor imagery (MI) is known to engage motor networks and could compensate for the maladaptive neuroplasticity elicited by immobilization.
This hypothesis and associated underlying neural mechanisms remain underexplored.
Here, we investigated how MI practice during 11 h of arm-immobilization influences sensorimotor and cortical representations of the hands, as well as sleep.
Fourteen participants were first tested after a normal day, followed by two 11-h periods of immobilization, either with concomitant MI treatment or control tasks.
Data revealed that MI prevented the consequences of immobilization: (i) alteration of the sensorimotor representation of hands, (ii) decrease of cortical excitability over the primary motor cortex (M1) contralateral to arm-immobilization, and (iii) reduction of sleep spindles over both M1s.
Furthermore, (iv) the time spent in REM sleep was significantly longer after MI.
These results support that implementing MI during immobilization can limit the deleterious effects of limb disuse, at several levels of sensorimotor functioning.

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