Evidence map›Paper›PMID 37968116›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2024

Dissociable Contributions of Basolateral Amygdala and Ventrolateral Orbitofrontal Cortex to Flexible Learning Under Uncertainty.

C G Aguirre, J H Woo, J L Romero-Sosa, Z M Rivera, A N Tejada, J J Munier, J Perez, M Goldfarb, K Das, M Gomez and 7 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 2 institutions in 2 countries.

C G AguirreDepartment of Psychology, University of California, Los Angeles, California 90095 cgaguirre@ucla.edu aizquie@psych.ucla.edu.
J H WooDepartment of Psychological and Brain Sciences, Dartmouth College, Hanover, New Hampshire 03755.ORCID 0009-0003-3534-206X
J L Romero-SosaDepartment of Psychology, University of California, Los Angeles, California 90095.
Z M RiveraDepartment of Psychology, University of California, Los Angeles, California 90095.
A N TejadaDepartment of Psychology, University of California, Los Angeles, California 90095.
J J MunierSection of Biosystems and Function, School of Dentistry, University of California, Los Angeles, California 90095.
J PerezDepartment of Psychology, University of California, Los Angeles, California 90095.
M GoldfarbDepartment of Psychology, University of California, Los Angeles, California 90095.
K DasDepartment of Psychology, University of California, Los Angeles, California 90095.
M GomezDepartment of Psychology, University of California, Los Angeles, California 90095.
T YeDepartment of Psychology, University of California, Los Angeles, California 90095.
J PannuSection of Biosystems and Function, School of Dentistry, University of California, Los Angeles, California 90095.
K EvansDepartment of Psychology, University of California, Los Angeles, California 90095.
P R O'NeillShirley and Stefan Hatos Center for Neuropharmacology, Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California 90095.
I SpigelmanSection of Biosystems and Function, School of Dentistry, University of California, Los Angeles, California 90095.
A SoltaniDepartment of Psychological and Brain Sciences, Dartmouth College, Hanover, New Hampshire 03755.ORCID 0000-0003-4386-8486
A IzquierdoDepartment of Psychology, University of California, Los Angeles, California 90095 cgaguirre@ucla.edu aizquie@psych.ucla.edu.ORCID 0000-0001-9897-2091
University of California, Los Angeles · USDartmouth College · US

Funding

CRCNS Research Proposal: Cortico-amygdalar substrates of adaptive learningR01DA047870 · NIDA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Alicia Izquierdo, Alireza Soltani · 2018 to 2026
$4.1M
Synaptic mechanisms of HPA axis dysregulation in alcohol dependenceR01AA024527 · NIAAA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SPIGELMAN, IGOR · 2016 to 2020
$1.7M
Training in Neurotechnology TranslationT32NS115753 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LU, DANIEL, MARKOVIC, DEJAN · 2020 to 2024
$1.2M
Nociceptin receptor signaling and regulation of dopamine transmission in drug reward circuitryK01DA042219 · NIDA · WASHINGTON UNIVERSITY · PI O'NEILL, PATRICK ROSS · 2017 to 2021
$715k
Frontocortical Signaling Signatures in Flexible Reinforcement LearningR21MH122800 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BLAIR, HUGH T, IZQUIERDO, ALICIA · 2021 to 2022
$429k
Sex differences in neuroendocrine mechanisms of HPA axis dysfunction in alcohol use disorderF31AA028183 · NIAAA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MUNIER, JOSEPH · 2020 to 2021
$75k
NIAAA NIH HHS F31 AA028183NIAAA NIH HHS R01 AA024527NIDA NIH HHS K01 DA042219NIDA NIH HHS R01 DA047870NIMH NIH HHS R21 MH122800NINDS NIH HHS T32 NS115753
6 · The paper itself

Abstract

Reversal learning measures the ability to form flexible associations between choice outcomes with stimuli and actions that precede them. This type of learning is thought to rely on several cortical and subcortical areas, including the highly interconnected orbitofrontal cortex (OFC) and basolateral amygdala (BLA), and is often impaired in various neuropsychiatric and substance use disorders. However, the unique contributions of these regions to stimulus- and action-based reversal learning have not been systematically compared using a chemogenetic approach particularly before and after the first reversal that introduces new uncertainty. Here, we examined the roles of ventrolateral OFC (vlOFC) and BLA during reversal learning. Male and female rats were prepared with inhibitory designer receptors exclusively activated by designer drugs targeting projection neurons in these regions and tested on a series of deterministic and probabilistic reversals during which they learned about stimulus identity or side (left or right) associated with different reward probabilities. Using a counterbalanced within-subject design, we inhibited these regions prior to reversal sessions. We assessed initial and pre-/post-reversal changes in performance to measure learning and adjustments to reversals, respectively. We found that inhibition of the ventrolateral orbitofrontal cortex (vlOFC), but not BLA, eliminated adjustments to stimulus-based reversals. Inhibition of BLA, but not vlOFC, selectively impaired action-based probabilistic reversal learning, leaving deterministic reversal learning intact. vlOFC exhibited a sex-dependent role in early adjustment to action-based reversals, but not in overall learning. These results reveal dissociable roles for BLA and vlOFC in flexible learning and highlight a more crucial role for BLA in learning meaningful changes in the reward environment.

Indexed as

Basolateral Nuclear ComplexAnimalsFemaleMalePrefrontal CortexRatsRats, Long-EvansReversal LearningUncertaintyaction learningdeterministicDREADDsprobabilisticreward learningstimulus learning

Identifiers

PMID37968116
PMCPMC10860573
OpenAlexW4388693084

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.