Evidence map›Paper›PMID 36607586›Full record

ArticleChinese journal of integrative medicine2023

Baicalin Ameliorates Corticosterone-Induced Depression by Promoting Neurodevelopment of Hippocampal via mTOR/GSK3β Pathway.

Zhe Wang, Ya-Ting Cheng, Ye Lu, Guo-Qiang Sun, Lin Pei

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In one paragraph

Article in Chinese journal of integrative medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Zhe WangSchool of Basic Medicine, Hebei University of Chinese Medicine, Shijiazhuang, 050200, China.
Ya-Ting ChengSchool of Basic Medicine, Hebei University of Chinese Medicine, Shijiazhuang, 050200, China.
Ye LuHebei Province Academy of Chinese Medicine Sciences, Shijiazhuang, 050031, China.
Guo-Qiang SunHebei Province Academy of Chinese Medicine Sciences, Shijiazhuang, 050031, China.
Lin PeiSchool of Basic Medicine, Hebei University of Chinese Medicine, Shijiazhuang, 050200, China. peilin13831190309@126.com.
Hebei University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the role of hippocampal neurodevelopment in the antidepressant effect of baicalin.

methodsForty male Institute of Cancer Research mice were divided into control, corticosterone (CORT, 40 mg/kg), CORT+baicalin-L (25 mg/kg), CORT+baicalin-H (50 mg/kg), and CORT+fluoxetine (10 mg/kg) groups according to a random number table. An animal model of depression was established by chronic CORT exposure. Behavioral tests were used to assess the reliability of depression model and the antidepressant effect of baicalin. In addition, Nissl staining and immunofluorescence were used to evaluate the effect of baicalin on hippocampal neurodevelopment in mice. The protein and mRNA expression levels of neurodevelopment-related factors were detected by Western blot analysis and real-time polymerase chain reaction, respectively.

resultsBaicalin significantly ameliorated the depressive-like behavior of mice resulting from CORT exposure and promoted the development of dentate gyrus in hippocampus, thereby reversing the depressive-like pathological changes in hippocampal neurons caused by CORT neurotoxicity. Moreover, baicalin significantly decreased the protein and mRNA expression levels of glycogen synthase kinase 3β (GSK3β), and upregulated the expression levels of cell cycle protein D1, p-mammalian target of rapamycin (mTOR), doublecortin, and brain-derived neurotrophic factor (all P<0.01). There were no significant differences between baicalin and fluoxetine groups (P>0.05).

conclusionBaicalin can promote the development of hippocampal neurons via mTOR/GSK3β signaling pathway, thus protect mice against CORT-induced neurotoxicity and play an antidepressant role.

Indexed as

CorticosteroneFluoxetineAnimalsAntidepressive AgentsBehavior, AnimalDepressionDisease Models, AnimalFlavonoidsGlycogen Synthase Kinase 3 betaHippocampusMaleMammalsMiceReproducibility of ResultsRNA, MessengerTOR Serine-Threonine KinasesAntidepressive AgentsbaicalinCorticosteroneFlavonoidsFluoxetineGlycogen Synthase Kinase 3 betaRNA, MessengerTOR Serine-Threonine Kinasesbaicalindepressionhippocampal neuronalmammalian target of rapamycin/glycogen synthase kinase 3β pathwayneurodevelopment

Identifiers

PMID36607586
OpenAlexW4313646686

What OpenQuestion holds

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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.