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  Modulation of neural activity in frontopolar cortex drives reward‑based motor learning

Herrojo-Ruiz, M., Maudrich, T., Kalloch, B., Sammler, D., Kenville, R., Villringer, A., et al. (2021). Modulation of neural activity in frontopolar cortex drives reward‑based motor learning. Scientific Reports, 11(1): 20303. doi:10.1038/s41598-021-98571-y.

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 Creators:
Herrojo-Ruiz, Maria1, 2, 3, Author
Maudrich, Tom3, Author           
Kalloch, Benjamin3, Author           
Sammler, Daniela4, Author           
Kenville, Rouven3, Author           
Villringer, Arno3, Author           
Sehm, Bernhard3, 5, Author           
Nikulin, Vadim V.2, 3, Author           
Affiliations:
1Department of Psychology, Goldsmiths, University of London, United Kingdom, ou_persistent22              
2Centre for Cognition and Decision Making, National Research University Higher School of Economics, Moscow, Russia, ou_persistent22              
3Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society, Leipzig, DE, ou_634549              
4Research Group Neurocognition of Music and Language, Max Planck Institute for Empirical Aesthetics, Frankfurt, Germany, ou_persistent22              
5Department of Neurology, Martin Luther University Halle-Wittenberg, Germany, ou_persistent22              

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Free keywords: Neuroscience; Psychology
 Abstract: 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.

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Language(s): eng - English
 Dates: 2021-03-102021-08-262021-10-13
 Publication Status: Published online
 Pages: -
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 Rev. Type: -
 Identifiers: DOI: 10.1038/s41598-021-98571-y
PMID: 34645848
PMC: PMC8514446
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Funding organization : Projekt DEAL
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Funding organization : International Engagement Fund of Goldsmiths University of London
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Funding organization : Basic Research Program of the National Research University Higher School of Economics (Russian Federation)

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Title: Scientific Reports
  Abbreviation : Sci. Rep.
Source Genre: Journal
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Publ. Info: London, UK : Nature Publishing Group
Pages: - Volume / Issue: 11 (1) Sequence Number: 20303 Start / End Page: - Identifier: ISSN: 2045-2322
CoNE: https://pure.mpg.de/cone/journals/resource/2045-2322