RESUMEN
The frontopolar cortex (FPC) contributes to tracking the reward of alternative choices during decision making, as well as their reliability. Whether this FPC function extends to reward gradients associated with continuous movements during motor learning remains unknown. We used anodal transcranial direct current stimulation (tDCS) over the right FPC to investigate its role in reward-based motor learning. Nineteen healthy human participants practiced novel sequences of finger movements on a digital piano with corresponding auditory feedback. Their aim was to use trialwise reward feedback to discover a hidden performance goal along a continuous dimension: timing. We additionally modulated the contralateral motor cortex (left M1) activity, and included a control sham stimulation. Right FPC-tDCS led to faster learning compared to lM1-tDCS and sham through regulation of motor variability. Bayesian computational modelling revealed that in all stimulation protocols, an increase in the trialwise expectation of reward was followed by greater exploitation, as shown previously. Yet, this association was weaker in lM1-tDCS suggesting a less efficient learning strategy. The effects of frontopolar stimulation were dissociated from those induced by lM1-tDCS and sham, as motor exploration was more sensitive to inferred changes in the reward tendency (volatility). The findings suggest that rFPC-tDCS increases the sensitivity of motor exploration to updates in reward volatility, accelerating reward-based motor learning.
Asunto(s)
Lóbulo Frontal/patología , Destreza Motora , Movimiento/fisiología , Adulto , Teorema de Bayes , Conducta , Electrodos , Femenino , Dedos/fisiología , Humanos , Aprendizaje , Masculino , Modelos Neurológicos , Corteza Motora , Neurociencias , Desempeño Psicomotor/fisiología , Reproducibilidad de los Resultados , Recompensa , Sensibilidad y Especificidad , Estimulación Transcraneal de Corriente Directa/métodos , Adulto JovenRESUMEN
Physiological mirror activity (pMA), observed in healthy human adults, describes the involuntary co-activation of contralateral homologous muscles during unilateral limb movements. Here we provide novel evidence, using neuromuscular measurements (electromyography; EMG), that the amplitude of pMA can be voluntarily inhibited during unilateral isometric contractions of intrinsic hand muscles after informing human participants (10 male, 10 female) about its presence and establishing a basic understanding of pMA mechanisms through a standardized protocol. Importantly, significant suppression of pMA was observed immediately after participants were asked to inhibit it, despite the absence of any online feedback during task execution and without special training. Moreover, we observed that the decrease of pMA was specifically accompanied by an increase in relative frontal δ power recorded with electroencephalography (EEG). Correlation analysis further revealed an inverse association between the individual amplitude of pMA and frontal δ power that reached significance once participants started to inhibit. Taken together, these results suggest that δ power in frontal regions might reflect executive processes exerting inhibitory control over unintentional motor output, in this case pMA. Our results provide an initial reference point for the development of therapeutic applications related to the neurorehabilitation of involuntary movements which could be realized through the suppression of pMA observed in the elderly before it would fully manifest in undesirable overt movement patterns.