Evidence map›Paper›PMID 36712944›Full record

ArticleDrug design, development and therapy2023

A Novel Approach Based on Gut Microbiota Analysis and Network Pharmacology to Explain the Mechanisms of Action of

Mukaram Amatjan, Na Li, Pengke He, Boheng Zhang, Xianyan Mai, Qianle Jiang, Haochen Xie, Xiaoni Shao

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

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  15. Frontiers in nutrition · 2024
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  16. Review
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  18. Article
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  20. Article
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

8 authors at 1 institution in 1 country.

Mukaram AmatjanImmunotherapy Laboratory, College of Pharmacology, Southwest Minzu University, Chengdu, 610225, People's Republic of China.
Na LiImmunotherapy Laboratory, College of Pharmacology, Southwest Minzu University, Chengdu, 610225, People's Republic of China.
Pengke HeImmunotherapy Laboratory, College of Pharmacology, Southwest Minzu University, Chengdu, 610225, People's Republic of China.
Boheng ZhangImmunotherapy Laboratory, College of Pharmacology, Southwest Minzu University, Chengdu, 610225, People's Republic of China.
Xianyan MaiImmunotherapy Laboratory, College of Pharmacology, Southwest Minzu University, Chengdu, 610225, People's Republic of China.
Qianle JiangImmunotherapy Laboratory, College of Pharmacology, Southwest Minzu University, Chengdu, 610225, People's Republic of China.
Haochen XieQinghai Tibet Plateau Research Institute, Southwest Minzu University, Chengdu, 610225, People's Republic of China.
Xiaoni ShaoImmunotherapy Laboratory, College of Pharmacology, Southwest Minzu University, Chengdu, 610225, People's Republic of China.
Southwest Minzu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Methods: CILF water extract was administered to an HN rat model established by adenine combined with ethambutol. The levels of uric acid (UA), serum urea nitrogen (UREA), and creatinine (CREA) were detected. Changes in the pathology and histology of the kidney were observed by hematoxylin-eosin staining. The 16S rRNA of the gut microbiota was sequenced. The binding ability of the main ingredients of CILF to key targets was analyzed by network pharmacology and molecular docking. The expression levels of the related mRNAs and proteins in the kidney were evaluated by RT-qPCR and immunohistochemistry analysis. Results: CILF administration significantly alleviated increases in UA, UREA, and CREA, structural damage, and kidney dysfunction. Gut microbiota analysis was applied to explore the pharmacological mechanism of the effects of CILF on bacterial diversity and microbiota structure in HN. CILF decreased the abundance of Conclusion: Our findings on the anti-HN effects of CILF and its mechanism of action, from the viewpoint of systems biology, and elaborated that CILF can alter the diversity and community structure of the gut microbiota in HN, providing new approaches for the prevention and treatment of HN.

Indexed as

Cichorium intybusDrugs, Chinese HerbalGastrointestinal MicrobiomeHyperuricemiaAdenineAnimalsCreatinineEthambutolMolecular Docking SimulationNetwork PharmacologyRatsRNA, Ribosomal, 16SUreaUric AcidAdenineCreatinineDrugs, Chinese HerbalEthambutolRNA, Ribosomal, 16SUreaUric AcidCichorium intybus L. formulagut microbiotahyperuricemic nephropathymolecular dockingnetwork pharmacology

Identifiers

PMID36712944
PMCPMC9880016
OpenAlexW4317470274

What OpenQuestion holds

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LicenceCC BY-NC
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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.