Evidence map›Paper›PMID 27840410›Full record

ArticleActa pharmacologica Sinica2017

Rheum emodin inhibits enterovirus 71 viral replication and affects the host cell cycle environment.

Ting Zhong, Li-Ying Zhang, Zeng-Yan Wang, Yue Wang, Feng-Mei Song, Ya-Hong Zhang, Jing-Hua Yu

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 42 citations in OpenAlex.

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  11. Emodin fromViruses · 2021
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  16. 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

7 authors at 4 institutions in 1 country.

Ting ZhongInstitute of Virology and AIDS Research, The First Hospital of Jilin University, Jilin University, Changchun 130000, China.
Li-Ying ZhangDepartment of Biotechnology, College of Animal Science and Veterinary Medicine, Jilin University, Changchun 130000, China.
Zeng-Yan WangDepartment of Internal Medicine, The First Hospital of Jilin University, Jilin University, Changchun 130000, China.
Yue WangChemistry of Traditional Chinese Medicine, College of Pharmacy, Changchun University of Chinese Medicine, Changchun 130000, China.
Feng-Mei SongDepartment of Experimental Pharmacology and Toxicology, School of Pharmacy, Jilin University, Changchun 130000, China.
Ya-Hong ZhangKey Laboratory of Natural Medicines and Immunotechnology of Henan Province, Henan University, Kaifeng 475004, china.
Jing-Hua YuInstitute of Virology and AIDS Research, The First Hospital of Jilin University, Jilin University, Changchun 130000, China.
Jilin University · CNFirst Hospital of Jilin University · CNChangchun University of Chinese Medicine · CNHenan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human enterovirus 71 (EV71) is the primary causative agent of recent large-scale outbreaks of hand, foot, and mouth disease (HFMD) in Asia. Currently, there are no drugs available for the prevention and treatment of HFMD. In this study, we compared the anti-EV71 activities of three natural compounds, rheum emodin, artemisinin and astragaloside extracted from Chinese herbs Chinese rhubarb, Artemisia carvifolia and Astragalus, respectively, which have been traditionally used for the treatment and prevention of epidemic diseases. Human lung fibroblast cell line MRC5 was mock-infected or infected with EV71, and treated with drugs. The cytotoxicity of the drugs was detected with MTT assay. The cytopathic effects such as cell death and condensed nuclei were morphologically observed. The VP1-coding sequence required for EV71 genome replication was assayed with qRT-PCR. Viral protein expression was analyzed with Western blotting. Viral TCID50 was determined to evaluate EV71 virulence. Flow cytometry analysis of propidium iodide staining was performed to analyze the cell cycle distribution of MRC5 cells. Rheum emodin (29.6 μmol/L) effectively protected MRC5 cells from EV71-induced cytopathic effects, which resulted from the inhibiting viral replication: rheum emodin treatment decreased viral genomic levels by 5.34-fold, viral protein expression by less than 30-fold and EV71 virulence by 0.33107-fold. The fact that inhibition of rheum emodin on viral virulence was much stronger than its effects on genomic levels and viral protein expression suggested that rheum emodin inhibited viral maturation. Furthermore, rheum emodin treatment markedly diminished cell cycle arrest at S phase in MRC5 cells, which was induced by EV71 infection and favored the viral replication. In contrast, neither astragaloside (50 μmol/L) nor artemisinin (50 μmol/L) showed similar anti-EV71 activities. Among the three natural compounds tested, rheum emodin effectively suppressed EV71 viral replication, thus is a candidate anti-HFMD drug.

Indexed as

AnimalsAntiviral AgentsArtemisininsCell CycleChlorocebus aethiopsEmodinEnterovirus A, HumanHost-Pathogen InteractionsHumansS PhaseVero CellsVirus ReplicationAntiviral AgentsartemisininArtemisininsEmodin

Identifiers

PMID27840410
PMCPMC5342659
OpenAlexW2555280827

What OpenQuestion holds

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Read underepoch 390

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.