Keyword search (4,163 papers available)

"Iordanova MD" Authored Publications:

Title Authors PubMed ID
1 Different behavioral measures of conditioned magazine activity can tell different stories about brain function Volz S; Loewinger G; Marquez I; Fevola S; Kang M; Reverte I; Krishnan A; Gardner MPH; Iordanova MD; Esber GR; 41922165
CSBN
2 Reduction in reward-driven behaviour depends on the basolateral but not central nucleus of the amygdala in female rats Lay BPP; Esber GR; Iordanova MD; 40925675
PSYCHOLOGY
3 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
4 The Rescorla-Wagner Model: It Is Not What You Think It Is Esber G; Schoenbaum G; Iordanova MD; 39805526
CSBN
5 OFC neurons do not represent the negative value of a conditioned inhibitor Esber GR; Usypchuk A; Saini S; Deroche M; Iordanova MD; Schoenbaum G; 38042330
CONCORDIA
6 Parvalbumin interneuron loss mediates repeated anesthesia-induced memory deficits in mice Roque PS; Thörn Perez C; Hooshmandi M; Wong C; Eslamizade MJ; Heshmati S; Brown N; Sharma V; Lister KC; Goyon VM; Neagu-Lund L; Shen C; Daccache N; Sato H; Sato T; Mogil JS; Nader K; Gkogkas CG; Iordanova MD; Prager-Khoutorsky M; McBride HM; Lacaille JC; Wykes L; Schricker T; Khoutorsky A; 36394958
PSYCHOLOGY
7 The Recruitment of a Neuronal Ensemble in the Central Nucleus of the Amygdala During the First Extinction Episode Has Persistent Effects on Extinction Expression Lay BPP; Koya E; Hope BT; Esber GR; Iordanova MD; 36336498
PSYCHOLOGY
8 Correction to: Persistent disruption of overexpectation learning after inactivation of the lateral orbitofrontal cortex in male rats Lay BPP; Choudhury R; Esber GR; Iordanova MD; 36006415
PSYCHOLOGY
9 Experimental chambers Persistent disruption of overexpectation learning after inactivation of the lateral orbitofrontal cortex in male rats Lay BPP; Choudhury R; Esber GR; Iordanova MD; 35932299
PSYCHOLOGY
10 Understanding Associative Learning Through Higher-Order Conditioning Gostolupce D; Lay BPP; Maes EJP; Iordanova MD; 35517574
PSYCHOLOGY
11 Agency rescues competition for credit assignment among predictive cues from adverse learning conditions Kang M; Reverte I; Volz S; Kaufman K; Fevola S; Matarazzo A; Alhazmi FH; Marquez I; Iordanova MD; Esber GR; 34376741
PSYCHOLOGY
12 Mechanisms of higher-order learning in the amygdala Gostolupce D; Iordanova MD; Lay BPP; 34197867
PSYCHOLOGY
13 Threat perception: Fear and the retrorubal field Bradfield LA; Iordanova MD; 34033766
CSBN
14 Neural substrates of appetitive and aversive prediction error. Iordanova MD, Yau JO, McDannald MA, Corbit LH 33453307
CSBN
15 Adaptive behaviour under conflict: deconstructing extinction, reversal, and active avoidance learning. Manning EE, Bradfield LA, Iordanova MD 33035525
CSBN
16 Different methods of fear reduction are supported by distinct cortical substrates. Lay BP, Pitaru AA, Boulianne N, Esber GR, Iordanova MD 32589138
PSYCHOLOGY
17 A self-initiated cue-reward learning procedure for neural recording in rodents. Reverte I, Volz S, Alhazmi FH, Kang M, Kaufman K, Chan S, Jou C, Iordanova MD, Esber GR 32135212
CSBN
18 Causal evidence supporting the proposal that dopamine transients function as temporal difference prediction errors. Maes EJP, Sharpe MJ, Usypchuk AA, Lozzi M, Chang CY, Gardner MPH, Schoenbaum G, Iordanova MD 31959935
CSBN
19 Neural correlates of two different types of extinction learning in the amygdala central nucleus. Iordanova MD, Deroche ML, Esber GR, Schoenbaum G 27531638
CSBN
20 Dopamine Signaling Is Critical for Supporting Cue-Driven Behavioral Control. Iordanova MD 31103706
PSYCHOLOGY
21 Thought control with the dopamine transient. Iordanova MD 30338459
CSBN
22 Dissociation of Appetitive Overexpectation and Extinction in the Infralimic Cortex. Lay BPP, Nicolosi M, Usypchuk AA, Esber GR, Iordanova MD 30371757
CSBN
23 Corrigendum: Dissociation of Appetitive Overexpectation and Extinction in the Infralimbic Cortex. Lay BPP, Nicolosi M, Usypchuk AA, Esber GR, Iordanova MD 30590441
CSBN
24 The serial blocking effect: a testbed for the neural mechanisms of temporal-difference learning. Mahmud A; Petrov P; Esber GR; Iordanova MD; 30979910
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.





BookR developed by Sriram Narayanan
for the Concordia University School of Health
Copyright © 2011-2026
Cookie settings
Concordia University