Dopamine transients are sufficient and necessary for acquisition of model-based associations

Learning to predict reward is thought to be driven by dopaminergic prediction errors, which reflect discrepancies between actual and expected value. Here the authors show that learning to predict neutral events is also driven by prediction errors and that such value-neutral associative learning is a...

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Vydané v:Nature neuroscience Ročník 20; číslo 5; s. 735 - 742
Hlavní autori: Sharpe, Melissa J, Chang, Chun Yun, Liu, Melissa A, Batchelor, Hannah M, Mueller, Lauren E, Jones, Joshua L, Niv, Yael, Schoenbaum, Geoffrey
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: New York Nature Publishing Group US 01.05.2017
Nature Publishing Group
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ISSN:1097-6256, 1546-1726, 1546-1726
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Shrnutí:Learning to predict reward is thought to be driven by dopaminergic prediction errors, which reflect discrepancies between actual and expected value. Here the authors show that learning to predict neutral events is also driven by prediction errors and that such value-neutral associative learning is also likely mediated by dopaminergic error signals. Associative learning is driven by prediction errors. Dopamine transients correlate with these errors, which current interpretations limit to endowing cues with a scalar quantity reflecting the value of future rewards. We tested whether dopamine might act more broadly to support learning of an associative model of the environment. Using sensory preconditioning, we show that prediction errors underlying stimulus–stimulus learning can be blocked behaviorally and reinstated by optogenetically activating dopamine neurons. We further show that suppressing the firing of these neurons across the transition prevents normal stimulus–stimulus learning. These results establish that the acquisition of model-based information about transitions between nonrewarding events is also driven by prediction errors and that, contrary to existing canon, dopamine transients are both sufficient and necessary to support this type of learning. Our findings open new possibilities for how these biological signals might support associative learning in the mammalian brain in these and other contexts.
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ISSN:1097-6256
1546-1726
1546-1726
DOI:10.1038/nn.4538