Keyword search (4,163 papers available)

"Optogenetics" Keyword-tagged Publications:

Title Authors PubMed ID
1 Smart Optogenetics for Real-Time Automated Control of Cardiac Electrical Activity Deng S; Harlaar N; Zhang J; Dekker SO; Kudryashova NN; Zhou H; Bart CI; Jin T; Derevyanko G; van Driel W; Panfilov AV; Poelma RH; de Vries AAF; Zhang G; De Coster T; Pijnappels DA; 41684280
CHEMBIOCHEM
2 Disentangling prediction error and value in a formal test of dopamine s role in reinforcement learning Usypchuk AA; Maes EJP; Lozzi M; Avramidis DK; Schoenbaum G; Esber GR; Gardner MPH; Iordanova MD; 40738112
CSBN
3 Corticostriatal suppression of appetitive Pavlovian conditioned responding Villaruel FR; Martins M; Chaudhri N; 34880119
PSYCHOLOGY
4 The trade-off between pulse duration and power in optical excitation of midbrain dopamine neurons approximates Bloch's law Pallikaras V; Carter F; Velazquez-Martinez DN; Arvanitogiannis A; Shizgal P; 34864162
PSYCHOLOGY
5 Seeing is believing: tools to study the role of Rho GTPases during cytokinesis Koh SP; Pham NP; Piekny A; 34405757
BIOLOGY
6 All-optical approaches to studying psychiatric disease Lafferty CK; Christinck TD; Britt JP; 34314828
CSBN
7 Off-Target Influences of Arch-Mediated Axon Terminal Inhibition on Network Activity and Behavior. Lafferty CK, Britt JP 32269514
CSBN
8 Nucleus Accumbens Cell Type- and Input-Specific Suppression of Unproductive Reward Seeking. Lafferty CK, Yang AK, Mendoza JA, Britt JP 32187545
CSBN
9 Hippocampal Input to the Nucleus Accumbens Shell Enhances Food Palatability. Yang AK, Mendoza JA, Lafferty CK, Lacroix F, Britt JP 31699294
CSBN
10 Cue-Evoked Dopamine Neuron Activity Helps Maintain but Does Not Encode Expected Value. Mendoza JA, Lafferty CK, Yang AK, Britt JP 31693885
CSBN

 

Title:Disentangling prediction error and value in a formal test of dopamine s role in reinforcement learning
Authors:Usypchuk AAMaes EJPLozzi MAvramidis DKSchoenbaum GEsber GRGardner MPHIordanova MD
Link:https://pubmed.ncbi.nlm.nih.gov/40738112/
DOI:10.1016/j.cub.2025.06.076
Publication:Current biology : CB
Keywords:Rescorla-Wagner modelchannelrhodopsinerror correctionmesolimbicoptogeneticsrodentscalar valuetemporal difference reinforcement learningtyrosine hydrohylase
PMID:40738112 Category: Date Added:2025-07-31
Dept Affiliation: CSBN
1 Department of Psychology, Centre for Studies in Behavioural Neurobiology, Concordia University, Montreal, QC H4B 1R6, Canada.
2 NIDA Intramural Research Program, Baltimore, MD 21224, USA; Departments of Anatomy & Neurobiology and Psychiatry, University of Maryland School of Medicine, Baltimore, MD 21201, USA; Solomon H. Snyder Department of Neuroscience, the Johns Hopkins University, Baltimore, MD 21287, USA.
3 Department of Psychology, Centre for Studies in Behavioural Neurobiology, Concordia University, Montreal, QC H4B 1R6, Canada. Electronic address: mihaela.iordanova@concordia.ca.

Description:

The discovery that midbrain dopamine (DA) transients can be mapped onto reward prediction errors (RPEs), the critical signal that drives learning, is a landmark in neuroscience. Causal support for the RPE hypothesis comes from studies showing that stimulating DA neurons can drive learning under conditions where it would not otherwise occur.1,2,3 However, such stimulation might also promote learning by adding reward value and indirectly inducing an RPE. This added value could support new learning even when it is insufficient to support instrumental behavior.4,5 Thus, these competing interpretations are challenging to disentangle and require direct comparison under matched conditions. We developed two computational models grounded in temporal difference reinforcement learning (TDRL)6,7,8 that dissociate the role of DA as an RPE versus a value signal. We validated our models by showing that they both predict learning (unblocking) when ventral tegmental area (VTA) DA stimulation occurs during expected reward delivery in a behavioral blocking design and confirmed this behaviorally. We then contrasted the models by delivering constant optogenetic stimulation during reward across both learning phases of blocking. The value model predicted blocking; the RPE model predicted unblocking. Behavioral results aligned with the latter. Moreover, the RPE model uniquely predicted that constant stimulation would unblock learning at higher frequencies (>20 Hz) when the artificial error alone drives learning. This, too, was confirmed experimentally. We demonstrate a principled computational and empirical dissociation between DA as an RPE versus a value signal. Our results advance understanding of how DA neuron stimulation drives learning.





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