4.7 Article

Variability in Dopamine Genes Dissociates Model-Based and Model-Free Reinforcement Learning

期刊

JOURNAL OF NEUROSCIENCE
卷 36, 期 4, 页码 1211-1222

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.1901-15.2016

关键词

decision-making; dopamine; genetics; reinforcement learning

资金

  1. National Institute of Mental Health [R01 MH080066-01]
  2. National Science Foundation [1460604]
  3. National Institute of Neurological Disorders and Stroke [R01NS078784]
  4. Direct For Social, Behav & Economic Scie
  5. Division Of Behavioral and Cognitive Sci [1460604] Funding Source: National Science Foundation

向作者/读者索取更多资源

Considerable evidence suggests that multiple learning systems can drive behavior. Choice can proceed reflexively from previous actions and their associated outcomes, as captured by model-free learning algorithms, or flexibly from prospective consideration of outcomes that might occur, as captured by model-based learning algorithms. However, differential contributions of dopamine to these systems are poorly understood. Dopamine is widely thought to support model-free learning by modulating plasticity in striatum. Model-based learning may also be affected by these striatal effects, or by other dopaminergic effects elsewhere, notably on prefrontal working memory function. Indeed, prominent demonstrations linking striatal dopamine to putatively model-free learning did not rule out model-based effects, whereas other studies have reported dopaminergic modulation of verifiably model-based learning, but without distinguishing a prefrontal versus striatal locus. To clarify the relationships between dopamine, neural systems, and learning strategies, we combine a genetic association approach in humans with two well-studied reinforcement learning tasks: one isolating model-based from model-free behavior and the other sensitive to key aspects of striatal plasticity. Prefrontal function was indexed by a polymorphism in the COMT gene, differences of which reflect dopamine levels in the prefrontal cortex. This polymorphism has been associated with differences in prefrontal activity and working memory. Striatal function was indexed by a gene coding for DARPP-32, which is densely expressed in the striatum where it is necessary for synaptic plasticity. We found evidence for our hypothesis that variations in prefrontal dopamine relate to model-based learning, whereas variations in striatal dopamine function relate to model-free learning.

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