Evidence map›Paper›PMID 34040346›Full record

ArticleDrug design, development and therapy2021

An Integrated Analysis of Network Pharmacology, Molecular Docking, and Experiment Validation to Explore the New Candidate Active Component and Mechanism of

Xue Bai, Yibo Tang, Qiang Li, Dan Liu, Guimin Liu, Xiaolei Fan, Zhejun Liu, Shujun Yu, Tian Tang, Shuyan Wang and 4 more

Open access · goldAbstract readValidation Study
In one paragraph

Article in Drug design, development and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 18 citations in OpenAlex.

  1. 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

14 authors at 1 institution in 1 country.

Xue BaiSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Yibo TangSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Qiang LiSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Dan LiuSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Guimin LiuSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Xiaolei FanSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Zhejun LiuSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Shujun YuSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Tian TangSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Shuyan WangSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Lingru LiNational Institute of TCM Constitution and Preventive Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Kailin ZhouSchool of Humanities, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Yanfei ZhengNational Institute of TCM Constitution and Preventive Medicine, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Zhenquan LiuSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Beijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOne of the most common types of male infertility is recognized as oligoasthenozoospermia (OA), characterized by low sperm count and quality in males. As a traditional Chinese medicine (TCM),

methodsHerein, an integrated approach, including network pharmacology, molecular docking, and experiment validation, was utilized to reveal the new candidate active component and mechanism of CSMFCH in treating OA.

resultsThe results show that kaempferol is the most significant bioactive component of CSMFCH on OA. The mechanism and targets of CSMFCH against OA are relevant to hormone regulation, oxidant stress, and reproductive promotion. In order to validate network pharmacology results, molecular docking and experiment validation were conducted. In detail, molecular docking was employed to verify the strong binding interactions between kaempferol and the core targets. UHPLC-Q-Orbitrap-MS was used to identify kaempferol in the CSMFCH extract. In vitro and in vivo experiments further proved CSMFCH and kaempferol could enhance the mouse Leydig (TM3) and mouse Sertoli (TM4) cell viability, improve the male reproductive organ weights, sperm quality, and decrease testis tissue damage in the OA mouse model induced by CP.

conclusionOur results not only identify the new candidate active component of CSMFCH in treating OA but also provide new insights into the mechanisms of CSMFCH against OA.

Indexed as

Molecular Docking SimulationAnimalsAsthenozoospermiaCell ProliferationCells, CulturedChromatography, High Pressure LiquidDisease Models, AnimalDrugs, Chinese HerbalFruitMaleMass SpectrometryMedicine, Chinese TraditionalMiceMice, Inbred StrainsPlant ExtractsDrugs, Chinese HerbalPlant Extractskaempferolnetwork pharmacologyoligoasthenozoospermiatraditional Chinese medicine

Identifiers

PMID34040346
PMCPMC8139735
OpenAlexW3160181045

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.