Evidence map›Paper›PMID 29752492›Full record

ArticlePsychopharmacology2018

Novel antidepressant effects of Paeonol alleviate neuronal injury with concomitant alterations in BDNF, Rac1 and RhoA levels in chronic unpredictable mild stress rats.

Xiu-Ling Zhu, Jing-Jing Chen, Fei Han, Chuan Pan, Ting-Ting Zhuang, Ya-Fei Cai, Ya-Ping Lu

Abstract read
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In one paragraph

Article in Psychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Molecular, Circuit, and Stress Response Characterization of Ventral Pallidum Npas1-Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
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  7. Multi-elements characteristic and potential risk of heavy metals in MOUTAN CORTEX from Anhui Province, China.International journal of environmental science and technology : IJEST · 2023
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Extract ofFrontiers in pharmacology · 2022
    Article
  13. Review
  14. Review
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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

7 authors at 2 institutions in 1 country.

Xiu-Ling ZhuCollege of Life Science, Anhui Normal University, Wuhu, 241000, China.
Jing-Jing ChenCollege of Life Science, Anhui Normal University, Wuhu, 241000, China.
Fei HanCollege of Life Science, Anhui Normal University, Wuhu, 241000, China.
Chuan PanCollege of Life Science, Anhui Normal University, Wuhu, 241000, China.
Ting-Ting ZhuangCollege of Life Science, Anhui Normal University, Wuhu, 241000, China.
Ya-Fei CaiCollege of Life Science, Anhui Normal University, Wuhu, 241000, China.
Ya-Ping LuCollege of Life Science, Anhui Normal University, Wuhu, 241000, China. yapinglu@ahnu.edu.cn.ORCID http://orcid.org/0000-0001-5371-0223
Anhui Normal University · CNWannan Medical College · CN

Funding

National Natural Science Foundation of China 30470537Natural Science Foundation of the Department of Education, Anhui Province ZD2008006-1
6 · The paper itself

Abstract

rationaleIncreasing evidence has suggested that major depressive disorder (MDD) is highly associated with brain-derived neurotrophic factor (BDNF) levels, dendrites atrophy, and loss of dendritic spines, especially in emotion-associated brain regions including the hippocampus. Paeonol is a kind of polyphenols natural product with a variety of therapeutic effects. Recent studies have reported its antidepressant effects. However, it is unclear what signaling pathways contribute to improve MDD.

objectiveThe present study investigated the effect of Paeonol on hippocampal neuronal morphology and its possible signaling pathways in chronic unpredictable mild stress (CUMS) rat model.

methodsUsing CUMS rat model, the antidepressant-like effect of Paeonol was validated via depression-related behavioral tests. Neuronal morphology in hippocampal CA1 and DG was assessed using ImageJ's Sholl plugin and RESCONSTRUCT software. BDNF signaling pathway-related molecules was determined by Western blotting.

resultsPaeonol attenuated CUMS-induced depression-like behaviors, which were accompanied by hippocampal neuronal morphological alterations. After Paeonol treatment for 4 weeks, the dendritic length and complexity and the density of dendritic spines markedly increased in the hippocampal CA1 and the dentate gyrus (DG). However, CUMS or Paeonol treatment does not selectively affect dendritic spine types. Simultaneously, administration of Paeonol deterred CUMS-induced cofilin1 activation that is essential for remolding of dendritic spines. The induction of CUMS downregulated BDNF levels and upregulated Rac1/RhoA levels; however, the tendency of these was inhibited by treatment with Paeonol.

conclusionOur data suggest that BDNF-Rac1/RhoA pathway may be involved in attenuation of CUMS-induced behavioral and neuronal damage by Paeonol that may represent a novel therapeutic agent for depression.

Indexed as

AcetophenonesAnimalsAntidepressive AgentsBrain-Derived Neurotrophic FactorChronic DiseaseDepressionHippocampusMaleNeuronsrac1 GTP-Binding ProteinRatsRats, Sprague-Dawleyrho GTP-Binding ProteinsStress, PsychologicalTreatment OutcomeAcetophenonesAntidepressive AgentsBdnf protein, ratBrain-Derived Neurotrophic Factorpaeonolrac1 GTP-Binding ProteinRac1 protein, ratRhoA protein, ratrho GTP-Binding ProteinsBDNFCofilin1Dendritic spineDepressionPaeonol

Identifiers

PMID29752492
OpenAlexW2801166011

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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 OpenQuestion graph.