Evidence map›Paper›PMID 33791372›Full record

ArticleBioMed research international2021

Agomelatine Softens Depressive-Like Behavior through the Regulation of Autophagy and Apoptosis.

Fengpei Chen, Shijia Chen, Jie Liu, Nashwa Amin, Weidong Jin, Marong Fang

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Neural plasticity and depression treatment.IBRO neuroscience reports · 2023
    Article
  5. Article
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Fengpei ChenThe Second Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou 310053, China.
Shijia ChenInstitute of Neuroscience, Zhejiang University School of Medicine, Hangzhou 310058, China.ORCID https://orcid.org/0000-0002-8361-2947
Jie LiuThe Second Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou 310053, China.
Nashwa AminInstitute of Neuroscience, Zhejiang University School of Medicine, Hangzhou 310058, China.
Weidong JinThe Second Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou 310053, China.ORCID https://orcid.org/0000-0001-7717-8470
Marong FangInstitute of Neuroscience, Zhejiang University School of Medicine, Hangzhou 310058, China.ORCID https://orcid.org/0000-0002-6636-4347
Zhejiang Chinese Medical University · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depression is a common and disabling mental disorder with high recurrence rate. Searching for more effective treatments for depression is a long-standing primary objective in neuroscience. Agomelatine (AGO) was reported as an antidepressant with unique pharmacological effects. However, its effects and the underlying mechanism are still unclear. In this study, we sought to evaluate the antidepressant effects of AGO on the chronic restraint stress (CRS) mouse model and preliminarily investigate its effects on the gut microbial metabolites. The CRS model mice were established in 28 days with AGO (60 mg/kg/day, by oral) or fluoxetine (15 mg/kg/day, by oral) administration. The number of behavioral tests was conducted to evaluate the effect of AGO on depression-like behavior alleviation. Meanwhile, the expression of the BDNF/TrkB/pERK signaling pathway, apoptosis, autophagy, and inflammatory protein markers were assessed using western blot and immunofluorescence. Our findings show that AGO can attenuate the depressive-like behavior that significantly appeared in both sucrose preference and forced swimming tests. Additionally, a noticeable upregulation of autophagy including Beclin1 and LC3II, microglial activity marker Iba-1, and BDNF/TrkB/pERK signaling pathways are indicated. An obvious decreased expression of NF-

Indexed as

DepressionStress, PsychologicalAcetamidesAnimalsApoptosisAutophagybcl-2-Associated X ProteinBehavior, AnimalBrain-Derived Neurotrophic FactorDisease Models, AnimalMaleMAP Kinase Signaling SystemMembrane GlycoproteinsMiceNaphthalenesProtein-Tyrosine KinasesAcetamidesagomelatineBax protein, mousebcl-2-Associated X ProteinBdnf protein, mouseBrain-Derived Neurotrophic FactorMembrane GlycoproteinsNaphthalenesNtrk2 protein, mouseProtein-Tyrosine KinasesReceptor, trkB

Identifiers

PMID33791372
PMCPMC7994102
OpenAlexW3137505329

What OpenQuestion holds

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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.