Evidence map›Paper›PMID 41371954›Full record

Trial reportThe Journal of neuroscience : the official journal of the Society for Neuroscience2026

Domain-General Neural Effects of Associative Learning and Expectations on Pain and Hedonic Taste Perception.

Yili Zhao, InSeon Lee, Margaret Rose-McCandlish, Qingbao Yu, Dominik Mischkowski, Jason A Avery, John E Ingeholm, Richard Reynolds, Gang Chen, Lauren Yvette Atlas

Erratum issuedAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2026. 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Yili ZhaoNational Center for Complementary and Integrative Health, National Institutes of Health, Bethesda, Maryland 20892 yili.zhao@nih.gov lauren.atlas@nih.gov.
InSeon LeeDepartment of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea.
Margaret Rose-McCandlishNational Center for Complementary and Integrative Health, National Institutes of Health, Bethesda, Maryland 20892.ORCID 0000-0002-1612-8493
Qingbao YuNational Center for Complementary and Integrative Health, National Institutes of Health, Bethesda, Maryland 20892.
Dominik MischkowskiDepartment of Psychology, University of Illinois, Champaign, Illinois 61820.
Jason A AveryNational Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892.ORCID 0000-0003-4097-2819
John E IngeholmNational Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892.ORCID 0000-0003-0327-5117
Richard ReynoldsNational Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892.
Gang ChenNational Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892.
Lauren Yvette AtlasNational Center for Complementary and Integrative Health, National Institutes of Health, Bethesda, Maryland 20892 yili.zhao@nih.gov lauren.atlas@nih.gov.ORCID 0000-0001-5693-4169

Funding

Neural and psychological mechanisms of pain perception ZIAAT000030 · NCCIH · NATIONAL CENTER FOR COMPLEMENTARY & INTEGRATIVE HEALTH · PI ATLAS, LAUREN · 2015 to 2025
$3.8M
Intramural NIH HHS ZIA AT000030
6 · The paper itself

Abstract

Predictive cues significantly influence perception through associative learning. However, it is unknown whether circuits are conserved across domains. We investigated how associative learning influences perceived intensity and valence of pain and hedonic taste and whether expectancy-based modulation varies by aversiveness or modality. Sixty participants (37 females, 23 males) were randomly assigned to receive either painful heat, unpleasant liquid saline, or pleasant liquid sucrose during fMRI scanning. Following conditioning, cues initially associated with low- or high-intensity outcomes were intermittently followed by stimuli calibrated to elicit medium-intensity ratings. Learned cues modulated expectations and subjective outcomes similarly across domains. Consistent with this, the orbitofrontal cortex exhibited domain-general anticipatory activation. Cue effects on perceived intensity and valence were mediated by the left anterior insula and thalamus, respectively-regions closely overlapping those identified in prior studies of pain expectancy (Atlas et al., 2010). Pain specificity was evident when we measured variations in stimulus intensity, whether we used univariate or multivariate approaches, but there was minimal evidence of specificity by modality or aversiveness in cue effects on medium trials. These findings suggest that shared neural circuits mediate the effects of learned expectations on perception, linking pain with other areas of affective processing and perception across domains.

Indexed as

Association LearningBrainPainPain PerceptionTaste PerceptionAdolescentAdultAnticipation, PsychologicalBrain MappingCuesFemaleHumansMagnetic Resonance ImagingMaleYoung Adultanterior insulaassociative learningexpectationorbitofrontal cortexpaintastes

Identifiers

PMID41371954
PMCPMC12828885

What OpenQuestion holds

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LicenceCC BY
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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.