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

Ruiz, M. H., 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: 20303. doi:10.1038/s41598-021-98571-y.

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Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.

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 Creators:
Ruiz, M. Herrojo1, 2, 3, Author
Maudrich, T.3, Author
Kalloch, B.3, Author
Sammler, Daniela4, Author           
Kenville, R.3, Author
Villringer, A.3, Author
Sehm, B.3, 5, Author
Nikulin, V. V.2, 3, Author
Affiliations:
1Psychology Department, Goldsmiths University of London, London, UK, ou_persistent22              
2Center for Cognition and Decision Making, National Research University Higher School of Economics, Moscow, Russian Federation, ou_persistent22              
3Department of Neurology, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany, ou_persistent22              
4Research Group Neurocognition of Music and Language, Max Planck Institute for Empirical Aesthetics, Max Planck Society, ou_3277646              
5Department of Neurology, University Hospital Halle (Saale), Halle, 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: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1038/s41598-021-98571-y
 Degree: -

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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 Sequence Number: 20303 Start / End Page: - Identifier: ISSN: 2045-2322
CoNE: https://pure.mpg.de/cone/journals/resource/2045-2322