Evidence map›Paper›PMID 31888678›Full record

ArticleMolecular brain2019

Proteomic profiling of the neurons in mice with depressive-like behavior induced by corticosterone and the regulation of berberine: pivotal sites of oxidative phosphorylation.

Qin Gong, Xiao-Jin Yan, Fan Lei, Mu-Lan Wang, Lu-Ling He, Ying-Ying Luo, Hong-Wei Gao, Yu-Lin Feng, Shi-Lin Yang, Jun Li and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular brain, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 23% of its field
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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 39 citations in OpenAlex.

  1. Brain Proteomic Responses to Glucocorticoids and Their Relationship With Transcriptome: A Systematic Meta-Analysis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  8. Therapeutic potential ofFrontiers in pharmacology · 2024
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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 at 3 institutions in 1 country.

Qin GongJiangxi University of Traditional Chinese Medicine, Nanchang, 330006, China.
Xiao-Jin YanSchool of Life Sciences, Tsinghua University, Beijing, 100084, China.
Fan LeiSchool of Life Sciences, Tsinghua University, Beijing, 100084, China.
Mu-Lan WangState Key Laboratory of Innovative Drugs and Efficient Energy-saving Pharmaceutical Equipment, Jiangxi University of Traditional Chinese Medicine, Nanchang, 330006, China.
Lu-Ling HeJiangxi University of Traditional Chinese Medicine, Nanchang, 330006, China.
Ying-Ying LuoJiangxi University of Traditional Chinese Medicine, Nanchang, 330006, China.
Hong-Wei GaoCollege of Pharmacy, Guangxi University of Chinese Medicine, Nanning, 530000, China.
Yu-Lin FengJiangxi University of Traditional Chinese Medicine, Nanchang, 330006, China.
Shi-Lin YangJiangxi University of Traditional Chinese Medicine, Nanchang, 330006, China.
Jun LiJiangxi University of Traditional Chinese Medicine, Nanchang, 330006, China. 21363492@qq.com.ORCID 0000-0002-2868-9511
Li-Jun DuJiangxi University of Traditional Chinese Medicine, Nanchang, 330006, China.
Jiangxi University of Traditional Chinese Medicine · CNTsinghua University · CNGuangxi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic corticosterone (CORT) stress is an anxiety and depression inducing factor that involves the dysfunction of glucocorticoid receptor (GR), brain-derived neurotrophic factor (BDNF), and neuronal plasticity. However, the regulation of proteomic profiles in neurons suffering CORT stress is remaining elusive. Thus, the proteomic profiles of mouse neuronal C17.2 stem cells were comprehensively investigated by TMT (tandem mass tag)-labeling quantitative proteomics. The quantitative proteomics conjugated gene ontology analysis revealed the inhibitory effect of CORT on the expression of mitochondrial oxidative phosphorylation-related proteins, which can be antagonized by berberine (BBR) treatment. In addition, animal studies showed that changes in mitochondria by CORT can affect neuropsychiatric activities and disturb the physiological functions of neurons via disordering mitochondrial oxidative phosphorylation. Thus, the mitochondrial energy metabolism can be considered as one of the major mechanism underlying CORT-mediated depression. Since CORT is important for depression after traumatic stress disorder, our study will shed light on the prevention and treatment of depression as well as posttraumatic stress disorder (PTSD).

Indexed as

Behavior, AnimalProteomicsAnimalsBerberineCell SurvivalCorticosteroneDepressionDisease Models, AnimalDown-RegulationGene Expression RegulationMaleMice, Inbred C57BLMitochondriaNeuronsOxidative PhosphorylationReproducibility of ResultsBerberineCorticosteroneRNA, MessengerBerberineCorticosteroneDepressionMitochondriaProteomic analysis

Identifiers

PMID31888678
PMCPMC6937859
OpenAlexW2998219777

What OpenQuestion 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 OpenQuestion graph.