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
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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
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4 The Rescorla-Wagner Model: It Is Not What You Think It Is Esber G; Schoenbaum G; Iordanova MD; 39805526
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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
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14 Neural substrates of appetitive and aversive prediction error. Iordanova MD, Yau JO, McDannald MA, Corbit LH 33453307
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15 Adaptive behaviour under conflict: deconstructing extinction, reversal, and active avoidance learning. Manning EE, Bradfield LA, Iordanova MD 33035525
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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
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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
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19 Neural correlates of two different types of extinction learning in the amygdala central nucleus. Iordanova MD, Deroche ML, Esber GR, Schoenbaum G 27531638
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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
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22 Dissociation of Appetitive Overexpectation and Extinction in the Infralimic Cortex. Lay BPP, Nicolosi M, Usypchuk AA, Esber GR, Iordanova MD 30371757
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23 Corrigendum: Dissociation of Appetitive Overexpectation and Extinction in the Infralimbic Cortex. Lay BPP, Nicolosi M, Usypchuk AA, Esber GR, Iordanova MD 30590441
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24 The serial blocking effect: a testbed for the neural mechanisms of temporal-difference learning. Mahmud A; Petrov P; Esber GR; Iordanova MD; 30979910
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Title:Reduction in reward-driven behaviour depends on the basolateral but not central nucleus of the amygdala in female rats
Authors:Lay BPPEsber GRIordanova MD
Link:https://pubmed.ncbi.nlm.nih.gov/40925675/
DOI:10.1523/JNEUROSCI.0288-25.2025
Publication:The Journal of neuroscience : the official journal of the Society for Neuroscience
Keywords:
PMID:40925675 Category: Date Added:2025-09-10
Dept Affiliation: PSYCHOLOGY
1 Center for Studies in Behavioural Neurobiology, Department of Psychology, Concordia University, Montreal, QC, Canada, H4B 1R6.
2 Center for Studies in Behavioural Neurobiology, Department of Psychology, Concordia University, Montreal, QC, Canada, H4B 1R6 mihaela.iordanova@concordia.ca.

Description:

Adaptive behavior depends on a dynamic balance between acquisition and extinction memories. Male and female rodents differ in extinction learning rates, suggestion potential sex-based differences in this balance. In males, deletion of extinction-recruited neurons in the central nucleus (CN) of the amygdala impairs extinction retrieval, shifting behavior toward acquisition (Lay et al., 2023). Here, we tested whether this mechanism also operates in females. In contrast to previously reported findings in males, deleting extinction-recruited CN neurons after single or extended extinction training had no effect on extinction retrieval in female rats. This lack of behavioral impact was not due to sex differences in CN activation during extinction. However, during early extinction, females showed greater activity in the basolateral amygdala (BLA) than males. Deletion of this BLA ensemble produced a more substantial reduction in conditioned approach than in non-deletion controls. These findings uncover a potential interplay between the CN and BLA in regulating conditioned approach in females. While ablation of extinction-recruited CN neurons do not modulate extinction retrieval in females, targeted BLA neuronal ablation during early extinction shifts behavior toward low, extinction-level responding. Thus heightened BLA activation during early extinction may prevent the emergence of extinction-like behavior in females. These findings, taken together with those reported by Lay et al. (2023) offer new insights into potential sex-based differences in the neural mechanisms underlying extinction and may inform the development of sex-based treatments for cue-triggered appetitive behaviors.Significance Statement This manuscript uncovers a neural mechanism that explains why females take longer to inhibit previously learned behavior. Together with findings reported in Lay et al. (2023), we uncover that the BLA and CN play complementary roles in balancing acquisition and extinction memories-BLA supports acquisition-based responses, which dominate during the early stages of extinction in females, while CN facilitates extinction-based responding, which develops faster in males. The CN-dependent extinction process, however, was not obtained in the females. This novel mechanism may account for the observed sex differences in disorders where competing memories influence behavior, such as drug abuse versus abstinence or anxiety versus cue-exposure therapy.





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