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Action sequence dynamics rely on accessory hyperdirect pathway-related targets in the striatum

View ORCID ProfileLachlan A. Ferguson, View ORCID ProfileMiriam Matamales, View ORCID ProfileBernard W. Balleine, View ORCID ProfileJesus Bertran-Gonzalez
doi: https://doi.org/10.1101/2022.03.28.486040
Lachlan A. Ferguson
1Decision Neuroscience Laboratory, School of Psychology, University of New South Wales, Sydney, NSW, Australia
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  • ORCID record for Lachlan A. Ferguson
  • For correspondence: lachlan_ferguson@hotmail.com j.bertran@unsw.edu.au
Miriam Matamales
1Decision Neuroscience Laboratory, School of Psychology, University of New South Wales, Sydney, NSW, Australia
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  • ORCID record for Miriam Matamales
Bernard W. Balleine
1Decision Neuroscience Laboratory, School of Psychology, University of New South Wales, Sydney, NSW, Australia
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Jesus Bertran-Gonzalez
1Decision Neuroscience Laboratory, School of Psychology, University of New South Wales, Sydney, NSW, Australia
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  • ORCID record for Jesus Bertran-Gonzalez
  • For correspondence: lachlan_ferguson@hotmail.com j.bertran@unsw.edu.au
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Abstract

Performing several actions in swift succession is often necessary to exploit known contingencies in the environment. However, after a change in the contingency rules, the ability to appropriately adapt rapid action sequences must be procured for continued success. By combining analyses of behavioural microstructure with circuit-specific tracing in mice, we report on a relationship between action timing-variability and successful adaptation that relies on post-synaptic targets of primary motor cortical (M1) projections to dorsolateral striatum (DLS). We found that M1 hyperdirect pathway projections to the STN also send dense axonal collaterals to external globus pallidus and dorsal striatum, with the highest synaptic volumes found in the DLS. Specific interruption of the M1→DLS circuit reduced the proportion of successful sequences while speeding-up and reducing action timing-variability, revealing a role for M1→DLS circuitry in setting the exploration/exploitation balance that is required for adaptively guiding the timing and success of instrumental action.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • Funding: This work was supported by an Australian Government Research Training Program Scholarship, a UNSW High Degree for Research Completion Scholarship and a UNSW Writing Scholarship to L.A.F., as well as by Australian Research Council (DP190102511, DP210102700) and the National Health and Medical Research Council (APP1165990) grants to J.B.G. and M.M.

  • Competing interests: The authors have no competing interests.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted March 29, 2022.
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Action sequence dynamics rely on accessory hyperdirect pathway-related targets in the striatum
Lachlan A. Ferguson, Miriam Matamales, Bernard W. Balleine, Jesus Bertran-Gonzalez
bioRxiv 2022.03.28.486040; doi: https://doi.org/10.1101/2022.03.28.486040
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Action sequence dynamics rely on accessory hyperdirect pathway-related targets in the striatum
Lachlan A. Ferguson, Miriam Matamales, Bernard W. Balleine, Jesus Bertran-Gonzalez
bioRxiv 2022.03.28.486040; doi: https://doi.org/10.1101/2022.03.28.486040

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