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Neural Correlates of Extinction in a Rat Model of Appetitive Pavlovian Conditioning

https://doi.org/10.1101/2022.09.28.509892

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.21679openalex-snapshot

Projections of the paraventricular and paratenial nuclei of the dorsal midline thalamus in the rat

inferredcites →https://doi.org/10.1002/syn.10279openalex-snapshot

Differential projections of the infralimbic and prelimbic cortex in the rat

inferredcites →https://doi.org/10.1007/s00213-001-0997-7openalex-snapshot

Basolateral amygdala inactivation abolishes conditioned stimulus- and heroin-induced reinstatement of extinguished heroin-seeking behavior in rats

inferredcites →https://doi.org/10.1007/s00213-002-1196-xopenalex-snapshot

Selective inactivation of the dorsomedial prefrontal cortex and the basolateral amygdala attenuates conditioned-cued reinstatement of extinguished cocaine-seeking behavior in rats

inferredcites →https://doi.org/10.1007/s00213-018-4957-xopenalex-snapshot

The role of the basolateral amygdala and infralimbic cortex in (re)learning extinction

inferredcites →https://doi.org/10.1007/s00213-018-5000-yopenalex-snapshot

A cFos activation map of remote fear memory attenuation

inferredcites →https://doi.org/10.1007/s00213-020-05454-7openalex-snapshot

Modulation of value-based decision making behavior by subregions of the rat prefrontal cortex

inferredcites →https://doi.org/10.1007/s00429-015-0997-8openalex-snapshot

Optogenetic inhibition of cortical afferents in the nucleus accumbens simultaneously prevents cue-induced transient synaptic potentiation and cocaine-seeking behavior

inferredcites →https://doi.org/10.1007/s00429-017-1475-2openalex-snapshot

Differential role of the anterior and intralaminar/lateral thalamic nuclei in systems consolidation and reconsolidation

inferredcites →https://doi.org/10.1007/s12264-020-00603-6openalex-snapshot

Projections from Infralimbic Cortex to Paraventricular Thalamus Mediate Fear Extinction Retrieval

inferredcites →https://doi.org/10.1016/0014-4886(63)90094-3openalex-snapshot

Conditioning and extinction of a food-rewarded response after selective ablations of frontal cortex in rhesus monkeys

inferredcites →https://doi.org/10.1016/0272-7358(91)90091-8openalex-snapshot

Sources of relapse after extinction in Pavlovian and instrumental learning

inferredcites →https://doi.org/10.1016/j.appet.2012.06.007openalex-snapshot

Learned food-cue stimulates persistent feeding in sated rats

inferredcites →https://doi.org/10.1016/j.bbr.2003.09.023openalex-snapshot

The role of prelimbic cortex in instrumental conditioning

inferredcites →https://doi.org/10.1016/j.bbr.2010.03.008openalex-snapshot

Opioid receptors in the basolateral amygdala but not dorsal hippocampus mediate context-induced alcohol seeking

inferredcites →https://doi.org/10.1016/j.bbr.2010.10.037openalex-snapshot

Extinction of drug seeking

inferredcites →https://doi.org/10.1016/j.beproc.2016.10.003openalex-snapshot

Occasion setting, inhibition, and the contextual control of extinction in Pavlovian and instrumental (operant) learning

inferredcites →https://doi.org/10.1016/j.biopsych.2005.12.015openalex-snapshot

Contextual and Temporal Modulation of Extinction: Behavioral and Biological Mechanisms

inferredcites →https://doi.org/10.1016/j.biopsych.2016.05.012openalex-snapshot

Circuit-Based Corticostriatal Homologies Between Rat and Primate

inferredcites →https://doi.org/10.1016/j.brainres.2014.12.024openalex-snapshot

Differential roles of medial prefrontal subregions in the regulation of drug seeking

inferredcites →https://doi.org/10.1016/j.celrep.2020.02.095openalex-snapshot

Nucleus Accumbens Cell Type- and Input-Specific Suppression of Unproductive Reward Seeking

inferredcites →https://doi.org/10.1016/j.cub.2016.12.052openalex-snapshot

A Functional Gradient in the Rodent Prefrontal Cortex Supports Behavioral Inhibition

inferredcites →https://doi.org/10.1016/j.neuron.2007.02.021openalex-snapshot

Consolidation of Fear Extinction Requires NMDA Receptor-Dependent Bursting in the Ventromedial Prefrontal Cortex

inferredcites →https://doi.org/10.1016/j.neuron.2009.03.005openalex-snapshot

The Orbitofrontal Cortex and Ventral Tegmental Area Are Necessary for Learning from Unexpected Outcomes

inferredcites →https://doi.org/10.1016/j.neuron.2015.10.044openalex-snapshot

Medial Orbitofrontal Cortex Mediates Outcome Retrieval in Partially Observable Task Situations

inferredcites →https://doi.org/10.1016/j.neuron.2017.03.036openalex-snapshot

Thalamic Regulation of Sucrose Seeking during Unexpected Reward Omission

inferredcites →https://doi.org/10.1016/j.neuropharm.2013.06.007openalex-snapshot

Extinction of drug seeking: Neural circuits and approaches to augmentation

inferredcites →https://doi.org/10.1016/j.neuropharm.2020.108007openalex-snapshot

Selective impact of lateral orbitofrontal cortex inactivation on reinstatement of alcohol seeking in male Long-Evans rats

inferredcites →https://doi.org/10.1016/j.neuroscience.2007.03.025openalex-snapshot

The role of different subregions of the basolateral amygdala in cue-induced reinstatement and extinction of food-seeking behavior

inferredcites →https://doi.org/10.1016/j.neuroscience.2010.04.018openalex-snapshot

Enhanced c-Fos expression in superior colliculus, paraventricular thalamus and septum during learning of cue-reward association

inferredcites →https://doi.org/10.1016/j.neuroscience.2011.09.004openalex-snapshot

A food predictive cue must be attributed with incentive salience for it to induce c-fos mRNA expression in cortico-striatal-thalamic brain regions

inferredcites →https://doi.org/10.1016/j.neuroscience.2016.10.043openalex-snapshot

A food-predictive cue attributed with incentive salience engages subcortical afferents and efferents of the paraventricular nucleus of the thalamus

inferredcites →https://doi.org/10.1016/j.nlm.2010.06.001openalex-snapshot

Lesion of infralimbic cortex occludes stress effects on retrieval of extinction but not fear conditioning

inferredcites →https://doi.org/10.1016/j.nlm.2013.08.002openalex-snapshot

Orbitofrontal cortex inactivation impairs between- but not within-session Pavlovian extinction: An associative analysis

inferredcites →https://doi.org/10.1016/j.nlm.2014.12.006openalex-snapshot

Inactivating the infralimbic but not prelimbic medial prefrontal cortex facilitates the extinction of appetitive Pavlovian conditioning in Long-Evans rats

inferredcites →https://doi.org/10.1016/j.nlm.2016.12.004openalex-snapshot

Sex specific recruitment of a medial prefrontal cortex-hippocampal-thalamic system during context-dependent renewal of responding to food cues in rats

inferredcites →https://doi.org/10.1016/j.nlm.2017.03.006openalex-snapshot

Distinct recruitment of basolateral amygdala-medial prefrontal cortex pathways across Pavlovian appetitive conditioning

inferredcites →https://doi.org/10.1016/s0006-3223(02)01546-9openalex-snapshot

Context, ambiguity, and unlearning: sources of relapse after behavioral extinction

inferredcites →https://doi.org/10.1037/0735-7044.118.2.389openalex-snapshot

Electrical Stimulation of Medial Prefrontal Cortex Reduces Conditioned Fear in a Temporally Specific Manner.

inferredcites →https://doi.org/10.1038/nature01138openalex-snapshot

Neurons in medial prefrontal cortex signal memory for fear extinction

inferredcites →https://doi.org/10.1038/nature06993openalex-snapshot

The role of the orbitofrontal cortex in the pursuit of happiness and more specific rewards

inferredcites →https://doi.org/10.1038/nature14030openalex-snapshot

A temporal shift in the circuits mediating retrieval of fear memory

inferredcites →https://doi.org/10.1038/nature15698openalex-snapshot

Basomedial amygdala mediates top-down control of anxiety and fear

inferredcites →https://doi.org/10.1038/npp.2010.184openalex-snapshot

Dissociable Roles of Prelimbic and Infralimbic Cortices, Ventral Hippocampus, and Basolateral Amygdala in the Expression and Extinction of Conditioned Fear

inferredcites →https://doi.org/10.1038/npp.2010.209openalex-snapshot

Interaction of the Basolateral Amygdala and Orbitofrontal Cortex is Critical for Drug Context-Induced Reinstatement of Cocaine-Seeking Behavior in Rats

inferredcites →https://doi.org/10.1038/npp.2014.314openalex-snapshot

Individual Variation in the Motivational and Neurobiological Effects of an Opioid Cue

inferredcites →https://doi.org/10.1038/s41398-018-0106-xopenalex-snapshot

Fear extinction requires infralimbic cortex projections to the basolateral amygdala

inferredcites →https://doi.org/10.1038/s41593-019-0361-zopenalex-snapshot

Distinct hippocampal engrams control extinction and relapse of fear memory

inferredcites →https://doi.org/10.1038/s41593-019-0572-3openalex-snapshot

Two genetically, anatomically and functionally distinct cell types segregate across anteroposterior axis of paraventricular thalamus

inferredcites →https://doi.org/10.1038/sj.npp.1300579openalex-snapshot

The Role of the Dorsomedial Prefrontal Cortex, Basolateral Amygdala, and Dorsal Hippocampus in Contextual Reinstatement of Cocaine Seeking in Rats

inferredcites →https://doi.org/10.1073/pnas.0909359107openalex-snapshot

Prelimbic cortical BDNF is required for memory of learned fear but not extinction or innate fear

inferredcites →https://doi.org/10.1073/pnas.1114415109openalex-snapshot

Contextual encoding by ensembles of medial prefrontal cortex neurons

inferredcites →https://doi.org/10.1073/pnas.1507611112openalex-snapshot

Prefrontal neurons encode context-based response execution and inhibition in reward seeking and extinction

inferredcites →https://doi.org/10.1093/cercor/bhn099openalex-snapshot

Dissociable Roles for the Ventromedial Prefrontal Cortex and Amygdala in Fear Extinction: NR2B Contribution

inferredcites →https://doi.org/10.1093/cercor/bhx275openalex-snapshot

Optogenetic Activation of the Infralimbic Cortex Suppresses the Return of Appetitive Pavlovian-Conditioned Responding Following Extinction

inferredcites →https://doi.org/10.1101/lm.1041309openalex-snapshot

Extinction circuits for fear and addiction overlap in prefrontal cortex

inferredcites →https://doi.org/10.1101/lm.1080108openalex-snapshot

Distinct contributions of the basolateral amygdala and the medial prefrontal cortex to learning and relearning extinction of context conditioned fear

inferredcites →https://doi.org/10.1101/lm.1463909openalex-snapshot

Reciprocal patterns of c-Fos expression in the medial prefrontal cortex and amygdala after extinction and renewal of conditioned fear

inferredcites →https://doi.org/10.1101/lm.1474609openalex-snapshot

Inactivation of the infralimbic but not the prelimbic cortex impairs consolidation and retrieval of fear extinction

inferredcites →https://doi.org/10.1101/lm.306106openalex-snapshot

Microstimulation reveals opposing influences of prelimbic and infralimbic cortex on the expression of conditioned fear

inferredcites →https://doi.org/10.1101/lm.78604openalex-snapshot

Delayed Recall of Fear Extinction in Rats With Lesions of Ventral Medial Prefrontal Cortex

inferredcites →https://doi.org/10.1101/lm.78704openalex-snapshot

Factors Regulating the Effects of Hippocampal Inactivation on Renewal of Conditional Fear After Extinction

inferredcites →https://doi.org/10.1101/lm.79704openalex-snapshot

Lesions of Rat Infralimbic Cortex Enhance Recovery and Reinstatement of an Appetitive Pavlovian Response

inferredcites →https://doi.org/10.1111/ejn.12283openalex-snapshot

A role for the ventral pallidum in context‐induced and primed reinstatement of alcohol seeking

inferredcites →https://doi.org/10.1111/j.1369-1600.2012.00479.xopenalex-snapshot

Optogenetic inhibition of cocaine seeking in rats

inferredcites →https://doi.org/10.1111/j.1460-9568.2007.05486.xopenalex-snapshot

Lesions of rat infralimbic cortex enhance renewal of extinguished appetitive Pavlovian responding

inferredcites →https://doi.org/10.1111/j.1460-9568.2007.05674.xopenalex-snapshot

Interactions of the basolateral amygdala with the dorsal hippocampus and dorsomedial prefrontal cortex regulate drug context‐induced reinstatement of cocaine‐seeking in rats

inferredcites →https://doi.org/10.1111/j.1460-9568.2009.06623.xopenalex-snapshot

Paraventricular thalamus mediates context‐induced reinstatement (renewal) of extinguished reward seeking

inferredcites →https://doi.org/10.1111/j.1460-9568.2009.06992.xopenalex-snapshot

Orbitofrontal inactivation impairs reversal of Pavlovian learning by interfering with ‘disinhibition’ of responding for previously unrewarded cues

inferredcites →https://doi.org/10.1111/j.1460-9568.2010.07223.xopenalex-snapshot

NMDA receptor antagonism in the basolateral but not central amygdala blocks the extinction of Pavlovian fear conditioning in rats

inferredcites →https://doi.org/10.1111/j.1460-9568.2012.07991.xopenalex-snapshot

Neural circuit competition in cocaine‐seeking: roles of the infralimbic cortex and nucleus accumbens shell

inferredcites →https://doi.org/10.1126/sciadv.1500251openalex-snapshot

Prefrontal inputs to the amygdala instruct fear extinction memory formation

inferredcites →https://doi.org/10.1126/science.aaw4325openalex-snapshot

Memory engrams: Recalling the past and imagining the future

inferredcites →https://doi.org/10.1146/annurev.neuro.24.1.897openalex-snapshot

Neurobiology of Pavlovian Fear Conditioning

inferredcites →https://doi.org/10.1152/physrev.00016.2020openalex-snapshot

Behavioral and neurobiological mechanisms of pavlovian and instrumental extinction learning

inferredcites →https://doi.org/10.1523/jneurosci.0054-10.2010openalex-snapshot

Inactivation of the Central But Not the Basolateral Nucleus of the Amygdala Disrupts Learning in Response to Overexpectation of Reward: Figure 1.

inferredcites →https://doi.org/10.1523/jneurosci.0140-16.2016openalex-snapshot

Distinct Fos-Expressing Neuronal Ensembles in the Ventromedial Prefrontal Cortex Mediate Food Reward and Extinction Memories

inferredcites →https://doi.org/10.1523/jneurosci.0684-15.2015openalex-snapshot

Losing Control: Excessive Alcohol Seeking after Selective Inactivation of Cue-Responsive Neurons in the Infralimbic Cortex

inferredcites →https://doi.org/10.1523/jneurosci.0773-16.2016openalex-snapshot

Chemogenetic Activation of an Extinction Neural Circuit Reduces Cue-Induced Reinstatement of Cocaine Seeking

inferredcites →https://doi.org/10.1523/jneurosci.0918-19.2019openalex-snapshot

Separate vmPFC Ensembles Control Cocaine Self-Administration Versus Extinction in Rats

inferredcites →https://doi.org/10.1523/jneurosci.1045-08.2008openalex-snapshot

Infralimbic Prefrontal Cortex Is Responsible for Inhibiting Cocaine Seeking in Extinguished Rats

inferredcites →https://doi.org/10.1523/jneurosci.1664-21.2021openalex-snapshot

Corticostriatal Suppression of Appetitive Pavlovian Conditioned Responding

inferredcites →https://doi.org/10.1523/jneurosci.1924-04.2004openalex-snapshot

Differential Involvement of Orbitofrontal Cortex Subregions in Conditioned Cue-Induced and Cocaine-Primed Reinstatement of Cocaine Seeking in Rats

inferredcites →https://doi.org/10.1523/jneurosci.20-16-06225.2000openalex-snapshot

The Role of Ventromedial Prefrontal Cortex in the Recovery of Extinguished Fear

inferredcites →https://doi.org/10.1523/jneurosci.3126-15.2015openalex-snapshot

Neural Estimates of Imagined Outcomes in Basolateral Amygdala Depend on Orbitofrontal Cortex

inferredcites →https://doi.org/10.1523/jneurosci.3137-14.2015openalex-snapshot

Revisiting the Role of Infralimbic Cortex in Fear Extinction with Optogenetics

inferredcites →https://doi.org/10.1523/jneurosci.3233-09.2009openalex-snapshot

Associatively Learned Representations of Taste Outcomes Activate Taste-Encoding Neural Ensembles in Gustatory Cortex

inferredcites →https://doi.org/10.1523/jneurosci.3821-16.2017openalex-snapshot

Extinction of Cocaine Seeking Requires a Window of Infralimbic Pyramidal Neuron Activity after Unreinforced Lever Presses

inferredcites →https://doi.org/10.1523/jneurosci.4079-10.2010openalex-snapshot

Medial Dorsal Hypothalamus Mediates the Inhibition of Reward Seeking after Extinction

inferredcites →https://doi.org/10.1523/jneurosci.4095-11.2011openalex-snapshot

Hippocampal and Prefrontal Projections to the Basal Amygdala Mediate Contextual Regulation of Fear after Extinction

inferredcites →https://doi.org/10.25080/tcwv9851openalex-snapshot

Exploring Network Structure, Dynamics, and Function using NetworkX

inferredcites →https://doi.org/10.3389/fnbeh.2013.00112openalex-snapshot

Differential Cortical c-Fos and Zif-268 Expression after Object and Spatial Memory Processing in a Standard or Episodic-Like Object Recognition Task

inferredcites →https://doi.org/10.3389/fnbeh.2013.00199openalex-snapshot

Ensemble coding of context-dependent fear memory in the amygdala

inferredcites →https://doi.org/10.3389/fnbeh.2020.598469openalex-snapshot

The Paraventricular Nucleus of the Thalamus Is an Important Node in the Emotional Processing Network

inferredcites →https://doi.org/10.3389/fnbeh.2021.665116openalex-snapshot

Time-Dependent Recruitment of Prelimbic Prefrontal Circuits for Retrieval of Fear Memory

inferredcites →https://doi.org/10.3389/fnins.2020.569517openalex-snapshot

Dissecting Neuronal Activation on a Brain-Wide Scale With Immediate Early Genes

inferredcites →https://doi.org/10.7554/elife.12248openalex-snapshot

RETRACTED: A mathematical model explains saturating axon guidance responses to molecular gradients

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