Evidence map›Paper›PMID 40568164›Full record

ArticlebioRxiv : the preprint server for biology2025

Domain-general neural effects of associative learning and expectations on pain and hedonic taste perception.

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

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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, United States.ORCID 0000-0003-4535-6636
In-Seon LeeDepartment of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
Margaret Rose-McCandlishNational Center for Complementary and Integrative Health, National Institutes of Health, Bethesda, Maryland, United States.
Qingbao YuNational Center for Complementary and Integrative Health, National Institutes of Health, Bethesda, Maryland, United States.
Dominik MischkowskiDepartment of Psychology, University of Illinois, Champaign, IL, United States.
Jason AveryNational Institute of Mental Health, Bethesda, Maryland, United States.
John E IngeholmNational Institute of Mental Health, Bethesda, Maryland, United States.
Richard ReynoldsNational Institute of Mental Health, Bethesda, Maryland, United States.
Gang ChenNational Institute of Mental Health, Bethesda, Maryland, United States.
Lauren AtlasNational Center for Complementary and Integrative Health, National Institutes of Health, Bethesda, Maryland, United States.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 the mechanisms that support expectancy-based modulation vary as a function of aversiveness and modality. Sixty participants were randomly assigned to receive either painful heat, unpleasant liquid saline, or pleasant liquid sucrose during fMRI scanning. Following conditioning, cues that were 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. The left anterior insula mediated domain-general cue effects on subjective intensity, whereas the thalamus mediated cue effects on subjective valence. Notably, these two regions were nearly identical to those previously implicated in mediating cue effects on pain (nearly identical to those previously implicated in cue effects on mediating pain (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 when we examined 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.

Identifiers

PMID40568164
PMCPMC12190406

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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.