Evidence map›Paper›PMID 40344568›Full record

ArticlePloS one2025

MiR-129-5p alleviates depression and anxiety by increasing astrocyte ATP production partly through targeting deubiquitinase Mysm1.

Qiaozhen Qin, Heyang Zhang, Xiaotong Li, Huaqiang Ruan, Shuirong Liu, Yue Chen, Zhenhua Xu, Yan Wang, Xinlong Yan, Xiaoxia Jiang

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

Qiaozhen QinBeijing Institute of Basic Medical Sciences, Haidian, Beijing, P.R. China.ORCID https://orcid.org/0009-0000-3164-7139
Heyang ZhangBeijing Institute of Basic Medical Sciences, Haidian, Beijing, P.R. China.
Xiaotong LiBeijing Institute of Basic Medical Sciences, Haidian, Beijing, P.R. China.
Huaqiang RuanBeijing Institute of Basic Medical Sciences, Haidian, Beijing, P.R. China.
Shuirong LiuBeijing Institute of Basic Medical Sciences, Haidian, Beijing, P.R. China.
Yue ChenBeijing Institute of Basic Medical Sciences, Haidian, Beijing, P.R. China.
Zhenhua XuBeijing Institute of Basic Medical Sciences, Haidian, Beijing, P.R. China.
Yan WangBeijing Institute of Basic Medical Sciences, Haidian, Beijing, P.R. China.
Xinlong YanBeijing International Science and Technology Cooperation Base for Antiviral Drugs, Beijing Key Laboratory of Environmental and Viral Oncology, College of Chemistry and Life Science, Beijing University of Technology, Beijing, China.
Xiaoxia JiangBeijing Institute of Basic Medical Sciences, Haidian, Beijing, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major depressive disorder (MDD) is a major global mental concern that severely affects quality of life, yet current pharmacological treatments remain limited in their effectiveness. Long-term chronic stress has been shown to increase the incidence of depression and anxiety. Micro RNAs (miRNAs) have been revealed to participate in the pathological process of depression and represent promising therapeutic targets. In this study, we found that microRNA-129-5p (miR-129-5p) was significantly decreased in the brains of depressive mice. Overexpression of miR-129-5p in the hippocampus effectively alleviated depressive-like behaviors and reduced the activation of microglial cells and astrocytes. In addition, ATP levels in depressive mice were significantly increased following miR-129-5p overexpression. The antidepressant effects of miR-129-5p were reversed when ATP function was blocked with the non-specific P2 receptor antagonist suramin. In vitro experiments revealed that miR-129-5p overexpression enhanced ATP production in astrocytes. Furthermore, using a dual-luciferase reporter assay, we found that miR-129-5p directly targeted Mysm1. When overexpressed in astrocytes, miR-129-5p significantly suppressed Mysm1 expression, promoted phosphorylation of p53 and AMPK, and enhanced the expression of PGC1α, factors previously associated with ATP production. Our findings highlight the crucial role of miR-129-5p in regulating depression, suggesting that miR-129-5p overexpression may serve as an effective strategy for antidepressant treatment.

Indexed as

Adenosine TriphosphateAnxietyAstrocytesDepressionMicroRNAsAnimalsHippocampusMaleMiceMice, Inbred C57BLAdenosine TriphosphateMicroRNAsMIRN129 microRNA, mouse

Identifiers

PMID40344568
PMCPMC12064192

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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.