Evidence map›Paper›PMID 29570670›Full record

ArticleInternational journal of molecular sciences2018

Oxymatrine Inhibits Influenza A Virus Replication and Inflammation via TLR4, p38 MAPK and NF-κB Pathways.

Jian-Ping Dai, Qian-Wen Wang, Yun Su, Li-Ming Gu, Hui-Xiong Deng, Xiao-Xuan Chen, Wei-Zhong Li, Kang-Sheng Li

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Article
  6. Article
  7. Article
  8. Article
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  13. Review
  14. Targeting natural products against SARS-CoV-2.Environmental science and pollution research international · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Refined polysaccharide fromFrontiers in immunology · 2022
    Article
  19. Article
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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

8 authors at 2 institutions in 2 countries.

Jian-Ping DaiDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou 515041, China. daijpedu2008@163.com.ORCID 0000-0002-8304-8207
Qian-Wen WangDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou 515041, China. 16qwwang1@stu.edu.cn.
Yun SuDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou 515041, China. yunsu1978@163.com.
Li-Ming GuDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou 515041, China. 13lmgu@stu.edu.cn.
Hui-Xiong DengDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou 515041, China. 15hxdeng@stu.edu.cn.
Xiao-Xuan ChenDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou 515041, China. xxchen85@stu.edu.cn.
Wei-Zhong LiDepartment of Veterinary Medicine, University of Maryland, College Park, MD 20742, USA. wzlistdxedu@sina.cn.
Kang-Sheng LiDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou 515041, China. liksedustdx@163.com.
Shantou University · CNUniversity of Maryland, College Park · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxymatrine (OMT) is a strong immunosuppressive agent that has been used in the clinic for many years. In the present study, by using plaque inhibition, luciferase reporter plasmids, qRT-PCR, western blotting, and ELISA assays, we have investigated the effect and mechanism of OMT on influenza A virus (IAV) replication and IAV-induced inflammation in vitro and in vivo. The results showed that OMT had excellent anti-IAV activity on eight IAV strains in vitro. OMT could significantly decrease the promoter activity of TLR3, TLR4, TLR7, MyD88, and TRAF6 genes, inhibit IAV-induced activations of Akt, ERK1/2, p38 MAPK, and NF-κB pathways, and suppress the expressions of inflammatory cytokines and MMP-2/-9. Activators of TLR4, p38 MAPK and NF-κB pathways could significantly antagonize the anti-IAV activity of OMT in vitro, including IAV replication and IAV-induced cytopathogenic effect (CPE). Furthermore, OMT could reduce the loss of body weight, significantly increase the survival rate of IAV-infected mice, decrease the lung index, pulmonary inflammation and lung viral titter, and improve pulmonary histopathological changes. In conclusion, OMT possesses anti-IAV and anti-inflammatory activities, the mechanism of action may be linked to its ability to inhibit IAV-induced activations of TLR4, p38 MAPK, and NF-κB pathways.

Indexed as

A549 CellsAlkaloidsAnimalsAntiviral AgentsCell LineDNA ReplicationDogsHumansInfluenza A virusMatrinesNF-kappa Bp38 Mitogen-Activated Protein KinasesQuinolizinesToll-Like Receptor 4AlkaloidsAntiviral AgentsMatrinesNF-kappa Boxymatrinep38 Mitogen-Activated Protein KinasesQuinolizinesToll-Like Receptor 4influenza A virusMAPKNF-κBOxymatrineTLR

Identifiers

PMID29570670
PMCPMC5979549
OpenAlexW2792884690

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.