Evidence map›Paper›PMID 29385192›Full record

ArticlePloS one2018

Anti-influenza A virus activity of rhein through regulating oxidative stress, TLR4, Akt, MAPK, and NF-κB signal pathways.

Qian-Wen Wang, Yun Su, Jiang-Tao Sheng, Li-Ming Gu, Ying Zhao, Xiao-Xuan Chen, Cheng Chen, Wei-Zhong Li, Kang-Sheng Li, Jian-Ping Dai

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
14.2field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 92 citations in OpenAlex.

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  20. Identification of Alkaloids fromChemistrySelect · 2022
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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

10 authors at 2 institutions in 2 countries.

Qian-Wen WangDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou, Guangdong, China.
Yun SuDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou, Guangdong, China.
Jiang-Tao ShengDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou, Guangdong, China.
Li-Ming GuDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou, Guangdong, China.
Ying ZhaoDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou, Guangdong, China.
Xiao-Xuan ChenDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou, Guangdong, China.
Cheng ChenDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou, Guangdong, China.
Wei-Zhong LiDepartment of Veterinary Medicine, University of Maryland, College Park, Maryland, United States of America.
Kang-Sheng LiDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou, Guangdong, China.
Jian-Ping DaiDepartment of Microbiology and Immunology, Shantou University Medical College, Shantou, Guangdong, China.ORCID 0000-0002-8304-8207
Shantou University · CNUniversity of Maryland, College Park · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rhein, an anthraquinone compound existing in many traditional herbal medicines, has anti-inflammatory, antioxidant, antitumor, antiviral, hepatoprotective, and nephroprotective activities, but its anti-influenza A virus (IAV) activity is ambiguous. In the present study, through plaque inhibition assay, time-of-addition assay, antioxidant assay, qRT-PCR, ELISA, and western blotting assays, we investigated the anti-IAV effect and mechanism of action of rhein in vitro and in vivo. The results showed that rhein could significantly inhibit IAV adsorption and replication, decrease IAV-induced oxidative stress, activations of TLR4, Akt, p38, JNK MAPK, and NF-κB pathways, and production of inflammatory cytokines and matrix metalloproteinases in vitro. Oxidant H2O2 and agonists of TLR4, Akt, p38/JNK and IKK/NF-κB could significantly antagonize the inhibitory effects of rhein on IAV-induced cytopathic effect (CPE) and IAV replication. Through an in vivo test in mice, we also found that rhein could significantly improve the survival rate, lung index, pulmonary cytokines, and pulmonary histopathological changes. Rhein also significantly decreased pulmonary viral load at a high dose. In conclusion, rhein can inhibit IAV adsorption and replication, and the mechanism of action to inhibit IAV replication may be due to its ability to suppress IAV-induced oxidative stress and activations of TLR4, Akt, p38, JNK MAPK, and NF-κB signal pathways.

Indexed as

A549 CellsAnimalsAnthraquinonesAntiviral AgentsCytokinesDogsFemaleHumansInfluenza A Virus, H1N1 SubtypeLungMadin Darby Canine Kidney CellsMaleMAP Kinase Signaling SystemMatrix MetalloproteinasesMiceMice, Inbred C57BLAnthraquinonesAntiviral AgentsCytokinesMatrix MetalloproteinasesNF-kappa BProto-Oncogene Proteins c-aktrheinToll-Like Receptor 4

Identifiers

PMID29385192
PMCPMC5791991
OpenAlexW2791517235

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.