Evidence map›Paper›PMID 42763341›Full record

ArticleMolecular psychiatry2026

A circuit dissection of perception-action decoupling in S-ketamine-induced hallucination-like states.

Dijia Wang, Junnan Xu, Zhaoran Wang, Zhirui Liu, Ziqing He, Tianjie Xu, Bin Mei, Jiqian Zhang, Hu Liu, Zhilai Yang and 6 more

Abstract read
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In one paragraph

Article in Molecular psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

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4 · The record

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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

16 authors.

Dijia Wang *Department of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anesthesia and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0000-0003-4808-7451
Junnan Xu *MOE Frontier Science Center for Brain Science & Brain-Machine Integration, NHC and CAMS Key Laboratory of Medical Neurobiology, School of Brain Science and Brain Medicine, Zhejiang University, Hangzhou, China.ORCID http://orcid.org/0000-0001-9319-9159
Zhaoran Wang *Department of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anesthesia and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University, Hefei, China.
Zhirui Liu *College of Computer Science and Artificial Intelligence, Wenzhou University, Wenzhou, China.
Ziqing HeDepartment of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anesthesia and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University, Hefei, China.
Tianjie XuMOE Frontier Science Center for Brain Science & Brain-Machine Integration, NHC and CAMS Key Laboratory of Medical Neurobiology, School of Brain Science and Brain Medicine, Zhejiang University, Hangzhou, China.
Bin MeiDepartment of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anesthesia and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0009-0005-4790-5047
Jiqian ZhangDepartment of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anesthesia and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0000-0001-6360-1557
Hu LiuDepartment of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anesthesia and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University, Hefei, China.
Zhilai YangDepartment of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anesthesia and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0009-0003-0597-4269
Xiang RenThird Research Institute of Ministry of Public Security, Shanghai, China.
Junda NiShanghai EDA Biotechnology Co., Ltd., Shanghai, China.
Yi LiCollege of Computer Science and Artificial Intelligence, Wenzhou University, Wenzhou, China. leee@zju.edu.cn.ORCID http://orcid.org/0000-0001-8425-7871
Wei GongMOE Frontier Science Center for Brain Science & Brain-Machine Integration, NHC and CAMS Key Laboratory of Medical Neurobiology, School of Brain Science and Brain Medicine, Zhejiang University, Hangzhou, China. weigong@zju.edu.cn.ORCID http://orcid.org/0000-0001-5568-5930
Gaolin QiuDepartment of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anesthesia and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University, Hefei, China. 1615423688@qq.com.
Xuesheng LiuDepartment of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anesthesia and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University, Hefei, China. liuxuesheng@ahmu.edu.cn.ORCID http://orcid.org/0000-0003-3779-2964

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82571450National Natural Science Foundation of China (National Science Foundation of China) grant Nos. 82571450
6 · The paper itself

Abstract

Hallucinations are a core feature of several psychiatric disorders, but the circuit mechanisms that separate perception from behavioral output remain poorly defined. Here, we combined an auditory discrimination task with AI-based pose analysis to quantify S-ketamine-induced false auditory threat responses and behavioral disorganization in mice. Control assays, including sucrose preference, loss of righting reflex, and prepulse inhibition, indicated that these effects were not explained by anhedonia, anesthesia, or basic auditory deficits. Using in vivo fiber photometry, single-cell miniscope calcium imaging, and pathway-specific chemogenetic and optogenetic manipulations, we identified dissociable circuit contributions within convergent striatal pathways. The basolateral amygdala to caudal striatum pathway (BLA→TS) supported salience-weighted perceptual decisions and, when aberrantly recruited by S-ketamine, promoted auditory false alarms. In contrast, the medial prefrontal cortex to caudal striatum pathway (mPFC→TS) primarily shaped behavioral expression and, when dysregulated, generated disorganized action patterns. At the network level, S-ketamine shifted TS activity from a sparse, high-contrast state to a high-frequency, low-amplitude, diffusely coupled state, consistent with reduced integrative precision. Auditory cortex to TS inputs were not broadly suppressed, supporting pathway specificity. Bidirectional chemogenetic manipulation of BLA→TS and mPFC→TS pathways in drug-naive mice further supported the TS as an integrative node linking perceptual evaluation to behavioral output. Dexmedetomidine co-administration restored pathway-level temporal dynamics and reorganized TS network coupling without simply suppressing activity. Together, these findings define a circuit framework for NMDAR-antagonist-induced hallucination-like states and provide a mechanistic rationale for dexmedetomidine-mediated mitigation of S-ketamine-associated perceptual and behavioral disruption.

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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.