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<p>Animals often exhibit rapid action changes in context-switching environments. This study hypothesized that, compared to the expected outcome, an unexpected outcome leads to distinctly different action-selection strategies to guide rapid adaptation. We designed behavioral measures differentiating between trial-by-trial dynamics after expected and unexpected events. In various reversal learning data with different rodent species and task complexities, conventional learning models failed to replicate the choice behavior following an unexpected outcome. This discrepancy was resolved by the proposed model with two different decision variables contingent on outcome expectation: the <i>support-stay</i> and <i>conflict-shift</i> bias. Electrophysiological data analyses revealed that striatal neurons encode our model’s key variables. Furthermore, the inactivation of striatal direct and indirect pathways neutralizes the effect of past expected and unexpected outcomes, respectively, on the action-selection strategy following an unexpected outcome. Our study suggests unique roles of the striatum in arbitrating between different action selection strategies for few-shot adaptation.</p>

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Striatal arbitration between choice strategies guides few-shot adaptation

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年2月20日

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  • Minsu Abel Yang,
  • Min Whan Jung,
  • Sang Wan Lee

摘要

Animals often exhibit rapid action changes in context-switching environments. This study hypothesized that, compared to the expected outcome, an unexpected outcome leads to distinctly different action-selection strategies to guide rapid adaptation. We designed behavioral measures differentiating between trial-by-trial dynamics after expected and unexpected events. In various reversal learning data with different rodent species and task complexities, conventional learning models failed to replicate the choice behavior following an unexpected outcome. This discrepancy was resolved by the proposed model with two different decision variables contingent on outcome expectation: the support-stay and conflict-shift bias. Electrophysiological data analyses revealed that striatal neurons encode our model’s key variables. Furthermore, the inactivation of striatal direct and indirect pathways neutralizes the effect of past expected and unexpected outcomes, respectively, on the action-selection strategy following an unexpected outcome. Our study suggests unique roles of the striatum in arbitrating between different action selection strategies for few-shot adaptation.