Corticostriatal White Matter Integrity and Dopamine D1 Receptor Availability Predict Age Differences in Prefrontal Value Signaling during Reward Learning

Author:

de Boer Lieke1ORCID,Garzón Benjamín1ORCID,Axelsson Jan23,Riklund Katrine23,Nyberg Lars234,Bäckman Lars1,Guitart-Masip Marc15

Affiliation:

1. Neurobiology, Care Sciences and Society, Aging Research Center, Karolinska Institutet, Stockholm 171 65, Sweden

2. Department of Radiation Sciences, Diagnostic Radiology, University Hospital, Umeå University, Umeå SE-901 87, Sweden

3. Department of Integrative Medical Biology, Physiology, Umeå University, Umeå SE-901 87, Sweden

4. Umeå Center for Functional Brain Imaging, Umeå University, Umeå 907 36, Sweden

5. Max Planck UCL Centre for Computational Psychiatry and Ageing Research, University College London, London WC1B 5EH, UK

Abstract

AbstractProbabilistic reward learning reflects the ability to adapt choices based on probabilistic feedback. The dopaminergically innervated corticostriatal circuit in the brain plays an important role in supporting successful probabilistic reward learning. Several components of the corticostriatal circuit deteriorate with age, as it does probabilistic reward learning. We showed previously that D1 receptor availability in NAcc predicts the strength of anticipatory value signaling in vmPFC, a neural correlate of probabilistic learning that is attenuated in older participants and predicts probabilistic reward learning performance. We investigated how white matter integrity in the pathway between nucleus accumbens (NAcc) and ventromedial prefrontal cortex (vmPFC) relates to the strength of anticipatory value signaling in vmPFC in younger and older participants. We found that in a sample of 22 old and 23 young participants, fractional anisotropy in the pathway between NAcc and vmPFC predicted the strength of value signaling in vmPFC independently from D1 receptor availability in NAcc. These findings provide tentative evidence that integrity in the dopaminergic and white matter pathways of corticostriatal circuitry supports the expression of value signaling in vmPFC which supports reward learning, however, the limited sample size calls for independent replication. These and future findings could add to the improved understanding of how corticostriatal integrity contributes to reward learning ability.

Funder

Swedish Research Council

Humboldt Research Award

Jochnick Foundation

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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