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Abstract
The signed value and unsigned salience of reward prediction errors (RPEs) are critical to understanding reinforcement learning (RL) and cognitive control. Dorsomedial prefrontal cortex (dMPFC) and insula (INS) are key regions for integrating reward and surprise information, but conflicting evidence for both signed and unsigned activity has led to multiple proposals for the nature of RPE representations in these brain areas. Recently developed RL models allow neurons to respond differently to positive and negative RPEs. Here, we use intracranially recorded high frequency activity (HFA) to test whether this flexible asymmetric coding strategy captures RPE coding diversity in human INS and dMPFC. At the region level, we found a bias towards positive RPEs in both areas which paralleled behavioral adaptation. At the local level, we found spatially interleaved neural populations responding to unsigned RPE salience and valence-specific positive and negative RPEs. Furthermore, directional connectivity estimates revealed a leading role of INS in communicating positive and unsigned RPEs to dMPFC. These findings support asymmetric coding across distinct but intermingled neural populations as a core principle of RPE processing and inform theories of the role of dMPFC and INS in RL and cognitive control.
It is unclear how dorsomedial prefrontal cortex and insula represent reward prediction errors. Here, the authors analyze human intracranial data to reveal spatially mixed, asymmetric coding of valence-specific and unsigned reward prediction errors, with insula leading dorsomedial prefrontal cortex.
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1 University of California, San Francisco, Department of Neurology, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811); University of California, Berkeley, Helen Wills Neuroscience Institute, Berkeley, USA (GRID:grid.47840.3f) (ISNI:0000 0001 2181 7878)
2 University of California, Berkeley, Helen Wills Neuroscience Institute, Berkeley, USA (GRID:grid.47840.3f) (ISNI:0000 0001 2181 7878); Aarhus University & The Royal Academy of Music, Center for Music in the Brain, Aarhus, Denmark (GRID:grid.7048.b) (ISNI:0000 0001 1956 2722)
3 University of California, Berkeley, Helen Wills Neuroscience Institute, Berkeley, USA (GRID:grid.47840.3f) (ISNI:0000 0001 2181 7878)
4 California Pacific Medical Center, Department of Neurology and Neurosurgery, San Francisco, USA (GRID:grid.17866.3e) (ISNI:0000 0000 9823 4542); Yale School of Medicine, Department of Neurology, New Haven, USA (GRID:grid.47100.32) (ISNI:0000000419368710)
5 California Pacific Medical Center, Department of Neurology and Neurosurgery, San Francisco, USA (GRID:grid.17866.3e) (ISNI:0000 0000 9823 4542)
6 University of California, Davis, Department of Neurology, Davis, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684); University of California, Davis, Center for Mind and Brain, Davis, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684)
7 University of California, Berkeley, Helen Wills Neuroscience Institute, Berkeley, USA (GRID:grid.47840.3f) (ISNI:0000 0001 2181 7878); University of California, Berkeley, Department of Psychology, Berkeley, USA (GRID:grid.47840.3f) (ISNI:0000 0001 2181 7878)