Evidence map›Paper›PMID 36550591›Full record

ArticleCNS neuroscience & therapeutics2023

Antidepression of Xingpijieyu formula targets gut microbiota derived from depressive disorder.

Yannan Li, Lixuan Yang, Junnan Li, Wei Gao, Zhonghui Zhao, Kaiqiang Dong, Wenzhe Duan, Baoan Dai, Rongjuan Guo

Open access · goldAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 15 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

9 authors at 2 institutions in 1 country.

Yannan LiSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Lixuan YangSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Junnan LiSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Wei GaoDepartment of Mental Health, Tsinghua University Yuquan Hospital, Beijing, China.
Zhonghui ZhaoSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Kaiqiang DongSecond Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Wenzhe DuanSecond Clinical Medical College, Beijing University of Chinese 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
Beijing University of Chinese Medicine · CNBeijing Hua Xin Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis investigation aims to determine the antidepressant role of Xingpijieyu formula (XPJYF) mediated via gut microbiota (GM)-brain axis.

methodsWe collected fecal microbiota from patients with depressive disorder (DD) and cultured microbiota in vitro. Some of microbiota were transplanted into germ-free rats with the intragastric administration of XPJYF grain at the dose of 1.533 g/kg/day. The behaviors were studied by forced swimming test, open field test, sucrose preference test, and body weight. Products of hypothalamus-pituitary-adrenocortical (HPA) axis, neurotransmitter, and serum cytokines were investigated by enzyme linked immunosorbent assay. Glial fibrillary acidic protein (GFAP), a biomarker of astrocyte, was quantified using immunofluorescence. Microbiota culturing in vitro after XPJYF treatment was analyze by 16 s RNA sequencing technology. We used lipopolysaccharide (LPS) to mimic activated rat primary astrocyte in vitro. Brain-derived neurotrophic factor (BDNF), cytokines, and oxidative stress factors were determined by western blotting, and glycometabolism in astrocyte was investigated by 2-deoxy-D-glucose (2-DG) uptake, adenosine triphosphate (ATP), and glucose-1-phosphate (G1P) kits.

resultsMicrobiota composition during 8 mg/ml of XPJYF (H12-8) for 12 h showed the more consistency. Lactococcus is enriched in DD-derived microbiota composition, and Biffdobacterium and Lactobacillus in H12-8 group. GLUCOSE1PMETAB-PWY and PWY-7328 of which biofunctions were dominantly encoded by Biffdobacterium were the top two of altered pathways. XPJYF improved behaviors and repressed astrocyte activation in depression rats. XPJYF elevated 2-DG uptake, ATP, glucose-1-phosphate, and brain-derived neurotrophic factor (BDNF), and inhibited cytokines and oxidative stress in LPS-induced astrocyte.

conclusionXPJYF treatment targets inflammation, activation, and glycometabolim in astrocyte via gut microbiota modulation, thereby improve animal behaviors, HPA axis dysfunction, and neurotransmitter synthesis in depression rats.

Indexed as

Depressive DisorderGastrointestinal MicrobiomeAnimalsBrain-Derived Neurotrophic FactorCytokinesDepressionHypothalamo-Hypophyseal SystemLipopolysaccharidesPituitary-Adrenal SystemRatsStress, PsychologicalBrain-Derived Neurotrophic FactorCytokinesLipopolysaccharidesastrocytedepressive disorderglycometabolismgut microbiotatradition Chinse medicine

Identifiers

PMID36550591
PMCPMC9873506
OpenAlexW4312115376

What OpenQuestion holds

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LicenceCC BY
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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.