Human claustrum neurons encode uncertainty and prediction errors during aversive learning

Flexible behavior depends on continuous updating of internal models, yet the neural circuits coordinating this process remain poorly understood. The claustrum, which is reciprocally connected to nearly the entire neocortex, is uniquely positioned to influence cortical processing. Here we report single-neuron recordings from the human claustrum during aversive learning, with anterior cingulate cortex and amygdala recordings for comparison. Claustrum and anterior cingulate neurons displayed structured, task-related responses. Distinct subpopulations encoded stimulus onset and action-contingent outcomes, with outcome representations diverging between regions. Critically, both regions encoded model-derived latent variables, including uncertainty and prediction error, but with different temporal profiles; only the anterior cingulate carried uncertainty signals during the intertrial period, whereas both regions encoded uncertainty and prediction error during the active-avoidance period. By contrast, the amygdala showed minimal latent-variable modulation. These findings provide evidence that human claustrum neurons track higher-order cognitive variables not directly observable from sensory input and reveal dissociable roles for the claustrum and anterior cingulate cortex in tracking latent task states. Human claustrum neurons track uncertainty and prediction errors during aversive learning, suggesting a role for the claustrum in updating beliefs and guiding adaptive behavior in dynamic environments.

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Publication Details

Journal
Nature Neuroscience
Published
2026-10-06
DOI
https://doi.org/10.1038/s41593-026-02475-x
Primary Topic
Memory and Neural Mechanisms
Type
article
Field-Weighted Citation Impact
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article

Human claustrum neurons encode uncertainty and prediction errors during aversive learning

Christopher Pittenger, Alfred P. Kaye, Murat Günel, Xiaosi Gu et al.
Nature Neuroscience
Memory and Neural Mechanisms
article

Human claustrum neurons encode uncertainty and prediction errors during aversive learning

Christopher Pittenger, Alfred P. Kaye, Murat Günel, Xiaosi Gu, Mauricio Medina‐Pizarro, Eyiyemisi C. Damisah, Sami Obaïd, Arman Afrasiyabi, Rodrigo Dalvit Carvalho da Silva, Smita Krishnaswamy, Kevin Navin Sheth, John Harrison Krystal, Maximilian E. Dougherty, Toby Wise, Yajun Zhou, Mingyue Hu, Jonathan Barreto-Nieves
article en

Abstract

Flexible behavior depends on continuous updating of internal models, yet the neural circuits coordinating this process remain poorly understood. The claustrum, which is reciprocally connected to nearly the entire neocortex, is uniquely positioned to influence cortical processing. Here we report single-neuron recordings from the human claustrum during aversive learning, with anterior cingulate cortex and amygdala recordings for comparison. Claustrum and anterior cingulate neurons displayed structured, task-related responses. Distinct subpopulations encoded stimulus onset and action-contingent outcomes, with outcome representations diverging between regions. Critically, both regions encoded model-derived latent variables, including uncertainty and prediction error, but with different temporal profiles; only the anterior cingulate carried uncertainty signals during the intertrial period, whereas both regions encoded uncertainty and prediction error during the active-avoidance period. By contrast, the amygdala showed minimal latent-variable modulation. These findings provide evidence that human claustrum neurons track higher-order cognitive variables not directly observable from sensory input and reveal dissociable roles for the claustrum and anterior cingulate cortex in tracking latent task states. Human claustrum neurons track uncertainty and prediction errors during aversive learning, suggesting a role for the claustrum in updating beliefs and guiding adaptive behavior in dynamic environments.

Nature Neuroscience
King's College London (GB), Yale University (US), Instituto Nacional de Neurología y Neurocirugía (MX)
Openalex Percentile: Top 12%
Memory and Neural Mechanisms
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