Evidence map›Paper›PMID 41867091›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Neuromodulator Dynamics Underlying Associative Learning in the Ventral Striatum's Olfactory Tubercle.

Maojun Hong, Liuting Zou, Yiqing Chen, Juan Guo, Zhixiang Xu, Tong Ma, Shuaishuai Hu, Rongfeng K Hu

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. 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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Maojun HongShanghai Pudong Hospital, Institute for Translational Brain Research, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Fudan University, Shanghai, China.
Liuting ZouShanghai Pudong Hospital, Institute for Translational Brain Research, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Fudan University, Shanghai, China.
Yiqing ChenShanghai Pudong Hospital, Institute for Translational Brain Research, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Fudan University, Shanghai, China.
Juan GuoDepartment of Anesthesiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Zhixiang XuState Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Fudan University, Shanghai, China.ORCID https://orcid.org/0000-0002-0962-7702
Tong MaInstitute for Translational Brain Research, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Fudan University, Shanghai, China.
Shuaishuai HuShanghai Mental Health Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.ORCID https://orcid.org/0000-0001-9836-4774
Rongfeng K HuShanghai Pudong Hospital, Institute for Translational Brain Research, State Key Laboratory of Brain Function and Disorders, MOE Frontiers Center for Brain Science, Fudan University, Shanghai, China.ORCID https://orcid.org/0009-0000-0164-6215

Funding

China Postdoctoral Science Foundation 2023M730654 to J.GNational Natural Science Foundation of China 82201418 to J.GNational Natural Science Foundation of China 82301395 to R.K.HNational Science and Technology Innovation 2030 Major Projects of China 2022ZD0207300 to R.K.H
6 · The paper itself

Abstract

The brain's neuromodulatory systems-particularly dopamine (DA), serotonin (5-HT), acetylcholine (ACh), and norepinephrine (NE)-play a crucial role in reward processing and associative learning. The olfactory tubercle (OT), a region that overlaps with the olfactory cortex and ventral striatum, has been implicated in non-olfactory functions such as learning and motivation. Moreover, it receives dense innervation from multiple neuromodulator-producing brain regions. Yet, how neuromodulator dynamics in the OT encodes external rewards and shapes different forms of associative learning remains unclear. Using fiber photometry and genetically encoded sensors, we captured reward-evoked release patterns of four neuromodulators in the OT and tracked their dynamics across distinct learning processes. We uncover sex-specific, state-dependent, and type-selective response dynamics to external rewards. Moreover, OT neuromodulators encode reward learning and extinction in a sexually dimorphic and state-dependent manner. Notably, unlike the nucleus accumbens (NAc), OT dopamine does not encode reward prediction error. Finally, these neuromodulators dynamically track cue discrimination and reversal learning. Together, we present a systematic framework mapping how OT neuromodulation encodes reward processing and associative learning. This advances our understanding of OT's roles in both healthy cognition and neuropsychiatric disorders, such as addiction and depression.

Indexed as

Association LearningNeurotransmitter AgentsOlfactory TubercleVentral StriatumAnimalsDopamineFemaleMaleNorepinephrineRewardDopamineNeurotransmitter AgentsNorepinephrinedopaminelearningneuromodulator dynamicsolfactory tuberclereversalreward

Identifiers

PMID41867091
PMCPMC13252644

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.