Evidence map›Paper›PMID 42538392›Full record

ArticleMolecular psychiatry2026

MicroRNA-148a regulates depressive-like behaviors in mice via the Otx2/Dopaminergic signaling axis.

Yifan Tang, Huicong Feng, Yue Li, Lupeng Zhang, Chiwen Qu, Tianai Zhu, Doudou Zhang, Yi Wen, Xiaomin Zeng, Yong Zhang and 1 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.

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

11 authors.

Yifan Tang *Hunan Normal University Health Science Center, Changsha, Hunan, 410081, China.
Huicong Feng *Hunan Normal University Health Science Center, Changsha, Hunan, 410081, China.
Yue LiDepartment of Pathology, Xiangtan Central Hospital, Xiangtan, Hunan, 411100, China.
Lupeng ZhangDepartment of Statistics, College of Mathematics and Computer Science, Hunan Normal University, Changsha, Hunan, 410081, China.
Chiwen QuGuangxi Key Laboratory of Artificial Intelligence for Genetic Diseases of Long-dwelling Nationalities, Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, China. quchiwen@163.com.ORCID http://orcid.org/0000-0002-0674-3126
Tianai ZhuHunan Normal University Health Science Center, Changsha, Hunan, 410081, China.
Doudou ZhangHunan Normal University Health Science Center, Changsha, Hunan, 410081, China.
Yi WenHunan Normal University Health Science Center, Changsha, Hunan, 410081, China.
Xiaomin ZengDepartment of Epidemiology and Health Statistics, Xiangya Public Health School, Central South University, Changsha, Hunan, 410078, China.
Yong ZhangHunan Normal University Health Science Center, Changsha, Hunan, 410081, China. thaddeus@hunnu.edu.cn.ORCID http://orcid.org/0000-0002-6847-2608
Xiaoning PengHunan Normal University Health Science Center, Changsha, Hunan, 410081, China. pxiaoning@hunnu.edu.cn.ORCID http://orcid.org/0000-0001-9383-7608

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNA-148a (miR-148a) has been implicated in various neurological disorders, yet its specific function within the central nervous system remains elusive. In this study, conditional astrocyte-specific miR-148a knockout (cKO) and overexpression (KI) mouse models were established using CRISPR-Cas9 and Cre-loxP technology to elucidate its role in emotional and cognitive regulation. Behavioral analyses demonstrated that miR-148a overexpression induced marked anxiety- and depression-like behaviors, accompanied by astrocyte activation, neuronal ultrastructural damage, and disrupted synaptic morphology. Conversely, miR-148a deletion preserved neuronal integrity, improved synaptic architecture, and produced anxiolytic and antidepressant phenotypes with enhanced cognitive performance. Transcriptomic profiling identified the transcription factor Otx2 as a direct target of miR-148a, mediating downstream modulation of dopaminergic signaling and neurodevelopmental genes. Integrative metabolomic analysis further revealed coordinated alterations in neuroendocrine and neurotransmitter-associated metabolic pathways. Collectively, these findings demonstrate that miR-148a critically modulates astrocyte-neuron interactions and dopaminergic homeostasis through the OTX2 axis, contributing to mood and cognitive disturbances. This work provides mechanistic insight into miR-148a-mediated neuroregulation and highlights its potential as a therapeutic target for affective and cognitive disorders.

Identifiers

PMID42538392

What Socratic holds

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Registered trials

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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 Socratic graph.