Evidence map›Paper›PMID 35713215›Full record

ArticleCNS neuroscience & therapeutics2022

Shugan granule contributes to the improvement of depression-like behaviors in chronic restraint stress-stimulated rats by altering gut microbiota.

Junnan Li, Yannan Li, Wenzhe Duan, Zhonghui Zhao, Lixuan Yang, Wei Wei, Jingchun Li, Yang Li, Yao Yu, Baoan Dai and 1 more

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–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

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Junnan LiSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Yannan LiSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Wenzhe DuanSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Zhonghui ZhaoSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Lixuan YangSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Wei WeiSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Jingchun LiSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Yang LiBeijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Yao YuBeijing Changping Hospital of Integrated Chinese and Western Medicine, Beijing, China.
Baoan DaiSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Rongjuan GuoDepartment of Neurology, Dongfang Hospital Beijing University of Chinese Medicine, Beijing, China.ORCID 0000-0002-5480-398X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe investigation aims to evaluate the potential effect of Shugan Granule (SGKL) on the gut, brain, and behaviors in rats exposed to chronic restraint stress (CRS).

methodsThe fecal microbiota and metabolite changes were studied in rats exposed to CRS and treated with SGKL (0.1 mg/kg/day). Depressive behaviors of these rats were determined through an open-field experiment, forced swimming test, sucrose preference, and weighing. Moreover, LPS-stimulated microglia and CRS-stimulated rats were treated with SGKL to investigate the regulation between SGKL and the PI3K/Akt/pathway, which is inhibited by LY294002, a PI3K inhibitor.

results(i) SGKL improved the altered behaviors in CRS-stimulated rats; (ii) SGKL ameliorated the CRS-induced neuronal degeneration and tangled nerve fiber and also contributed to the recovery of intestinal barrier injury in these rats; (iii) SGKL inhibited the hippocampus elevations of TNF-α, IL-1β, and IL-6 in response to CRS modeling; (iv) based on the principal coordinates analysis (PCoA), SGKL altered α-diversity indices and shifted β-diversity in CRS-stimulated rats; (v) at the genus level, SGKL decreased the CRS-enhanced abundance of Bacteroides; (vi) Butyricimonas and Candidatus Arthromitus were enriched in SGKL-treated rats; (vii) altered gut microbiota and metabolites were correlated with behaviors, inflammation, and PI3K/Akt/mTOR pathway; (viii) SGKL increased the LPS-decreased phosphorylation of the PI3K/Akt/mTOR pathway in microglia and inhibited the LPS-induced microglial activation; (ix) PI3K/Akt/mTOR pathway inactivation reversed the SGKL effects in CRS rats.

conclusionSGKL targets the PI3K/Akt/mTOR pathway by altering gut microbiota and metabolites, which ameliorates altered behavior and inflammation in the hippocampus.

Indexed as

DepressionDrugs, Chinese HerbalGastrointestinal MicrobiomeStress, PsychologicalAnimalsChronic DiseaseInflammationLipopolysaccharidesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRatsRestraint, PhysicalTOR Serine-Threonine KinasesDrugs, Chinese HerbalLipopolysaccharidesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinaseschronic restraint stressdepression-like behaviorsgut metabolomegut microbiotaShugan granule

Identifiers

PMID35713215
PMCPMC9344086

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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.