Keyword search (4,163 papers available)

"conditioning" Keyword-tagged Publications:

Title Authors PubMed ID
1 Activating Group II Metabotropic Glutamate Receptors in the Basolateral Amygdala Inhibits Increases in Reward Seeking Triggered by Discriminative Stimuli in Rats LeCocq MR; Mainville-Berthiaume A; Laplante I; Samaha AN; 40341317
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2 Palatability attributed to alcohol and alcohol-paired flavors Valyear MD; Eustachon NM; Britt JP; 38430645
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3 Augmenting glutamatergic, but not dopaminergic, activity in the nucleus accumbens shell disrupts responding to a discrete alcohol cue in an alcohol context Valyear MD; Brown A; Deyab G; Villaruel FR; Lahlou S; Caporicci-Dinucci N; Chaudhri N; 38185906
PSYCHOLOGY
4 Learning from opioid withdrawal: Effects on striatal dopamine (Commentary on Ahn et al., 2023) Leyton M; Nikolic M; 38129315
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5 Does phasic dopamine release cause policy updates? Carter F; Cossette MP; Trujillo-Pisanty I; Pallikaras V; Breton YA; Conover K; Caplan J; Solis P; Voisard J; Yaksich A; Shizgal P; 38039083
PSYCHOLOGY
6 What is Learned Determines How Pavlovian Conditioned Fear is Consolidated in the Brain Leake J; Leidl DM; Lay BPP; Fam JP; Giles MC; Qureshi OA; Westbrook RF; Holmes NM; 37963767
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7 NMDA Receptors in the Basolateral Amygdala Complex Are Engaged for Pavlovian Fear Conditioning When an Animal's Predictions about Danger Are in Error Tuval Keidar 37607821
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8 Sub-hourly measurement datasets from 6 real buildings: Energy use and indoor climate Sartori I; Walnum HT; Skeie KS; Georges L; Knudsen MD; Bacher P; Candanedo J; Sigounis AM; Prakash AK; Pritoni M; Granderson J; Yang S; Wan MP; 37153123
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9 Danger Changes the Way the Brain Consolidates Neutral Information; and Does So by Interacting with Processes Involved in the Encoding of That Information Omar A Qureshi 36927572
PSYCHOLOGY
10 A new circuit underlying the renewal of appetitive Pavlovian responses: Commentary on Brown and Chaudhri (2022) Valyear MD; Britt JP; 36700576
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11 Optogenetic stimulation of infralimbic cortex projections to the paraventricular thalamus attenuates context-induced renewal Brown A; Chaudhri N; 36373226
PSYCHOLOGY
12 Learning processes in relapse to alcohol use: lessons from animal models Valyear MD; LeCocq MR; Brown A; Villaruel FR; Segal D; Chaudhri N; 36264342
PSYCHOLOGY
13 Alarm cues and alarmed conspecifics: neural activity during social learning from different cues in Trinidadian guppies Raina Fan 36043284
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14 Understanding Associative Learning Through Higher-Order Conditioning Gostolupce D; Lay BPP; Maes EJP; Iordanova MD; 35517574
PSYCHOLOGY
15 Prediction error determines whether NMDA receptors in the basolateral amygdala complex are involved in Pavlovian fear conditioning Williams-Spooner MJ; Delaney AJ; Westbrook RF; Holmes NM; 35410880
PSYCHOLOGY
16 Supplementary dataset of context-dependent conditioned responding to an alcohol-predictive cue in female and male rats Segal D; Valyear MD; Chaudhri N; 35330738
PSYCHOLOGY
17 Anterior cingulate neurons signal neutral cue pairings during sensory preconditioning Hart EE; Gardner MPH; Schoenbaum G; 34936884
PSYCHOLOGY
18 Corticostriatal suppression of appetitive Pavlovian conditioned responding Villaruel FR; Martins M; Chaudhri N; 34880119
PSYCHOLOGY
19 The Role of Context Conditioning in the Reinstatement of Responding to an Alcohol-Predictive Conditioned Stimulus LeCocq MR; Sun S; Chaudhri N; 34852244
PSYCHOLOGY
20 The role of context on responding to an alcohol-predictive cue in female and male rats Segal D; Valyear MD; Chaudhri N; 34742865
PSYCHOLOGY
21 Cocaine cue-induced mesocorticolimbic activation in cocaine users: Effects of personality traits, lifetime drug use, and acute stimulant ingestion D' Amour-Horvat V; Cox SML; Dagher A; Kolivakis T; Jaworska N; Leyton M; 34463411
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22 Mechanisms of higher-order learning in the amygdala Gostolupce D; Iordanova MD; Lay BPP; 34197867
PSYCHOLOGY
23 Cue-alcohol associative learning in female rats. Cofresí RU, Monfils MH, Chaudhri N, Gonzales RA, Lee HJ 31002878
PSYCHOLOGY
24 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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25 Comparing ABA, AAB, and ABC Renewal of Appetitive Pavlovian Conditioned Responding in Alcohol- and Sucrose-Trained Male Rats. Khoo SY, Sciascia JM, Brown A, Chaudhri N 32116588
PSYCHOLOGY
26 Context controls the timing of responses to an alcohol-predictive conditioned stimulus. Valyear MD, Chaudhri N 32017964
PSYCHOLOGY
27 Differential role of oxytocin and vasopressin in the conditioned ejaculatory preference of the male rat. Ménard S, Gelez H, Girard-Bériault F, Coria-Avila G, Pfaus JG 31194998
PSYCHOLOGY
28 The Role of Sleep in Learning Placebo Effects. Chouchou F, Dang-Vu TT, Rainville P, Lavigne G 30146053
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Title:Corticostriatal suppression of appetitive Pavlovian conditioned responding
Authors:Villaruel FRMartins MChaudhri N
Link:https://pubmed.ncbi.nlm.nih.gov/34880119/
DOI:10.1523/JNEUROSCI.1664-21.2021
Publication:The Journal of neuroscience : the official journal of the Society for Neuroscience
Keywords:Pavlovian conditioningextinctioninfralimbic cortexnucleus accumbensoptogeneticsventromedial prefrontal cortex
PMID:34880119 Category: Date Added:2021-12-09
Dept Affiliation: PSYCHOLOGY
1 Center for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Quebec, Canada fr.villaruel@gmail.com.
2 Center for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Quebec, Canada.

Description:

The capacity to suppress learned responses is essential for animals to adapt in dynamic environments. Extinction is a process by which animals learn to suppress conditioned responding when an expected outcome is omitted. The infralimbic cortex (IL) to nucleus accumbens shell (NAcS) neural circuit is implicated in suppressing conditioned responding after extinction, especially in the context of operant cocaine-seeking behaviour. However, the role of the IL-to-NAcS neural circuit in the extinction of responding to appetitive Pavlovian cues is unknown and the psychological mechanisms involved in response suppression following extinction are unclear. We trained male, Long-Evans rats to associate a 10 s auditory conditioned stimulus (CS; 14 trials per session) with a sucrose unconditioned stimulus (US; 0.2 mL per CS) in a specific context and then, following extinction in a different context, precipitated a renewal of CS responding by presenting the CS alone in the original Pavlovian conditioning context. Unilateral, optogenetic stimulation of the IL-to-NAcS circuit selectively during CS trials suppressed renewal. In a separate experiment, IL-to-NAcS stimulation suppressed CS responding regardless of prior extinction and impaired extinction retrieval. Finally, IL-to-NAcS stimulation during the CS did not suppress the acquisition of Pavlovian conditioning but was required for the subsequent expression of CS responding. These results are consistent with multiple studies showing that the IL-to-NAcS neural circuit is involved in the suppression of operant cocaine-seeking, extending these findings to appetitive Pavlovian cues. The suppression of appetitive Pavlovian responding following IL-to-NAcS circuit stimulation, however, does not appear to be an extinction-dependent process.SIGNIFICANCE STATEMENTExtinction is a form of inhibitory learning through which animals learn to suppress conditioned responding in the face of non-reinforcement. We investigated the role of the infralimbic (IL) cortex inputs to the nucleus accumbens shell (NAcS) in the extinction of responding to appetitive Pavlovian cues and the psychological mechanisms involved in response suppression following extinction. Using in vivo optogenetics, we found that stimulating the IL-to-NAcS neural circuit suppressed context-induced renewal of conditioned responding after extinction. In a separate experiment, stimulating the IL-to-NAcS circuit suppressed conditioned responding in an extinction-independent manner. These findings can be leveraged by future research aimed at understanding how corticostriatal circuits contribute to behavioural flexibility and mental disorders that involve the suppression of learned behaviours.





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