Evidence map›Paper›PMID 27128889›Full record

ArticleMolecules (Basel, Switzerland)2016

Forsythoside A Controls Influenza A Virus Infection and Improves the Prognosis by Inhibiting Virus Replication in Mice.

Li Deng, Peng Pang, Ke Zheng, Jiao Nie, Huachong Xu, Sizhi Wu, Jia Chen, Xiaoyin Chen

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 3 pooled it
0.9field-weighted citation impact, top 26% 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, 3 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. International journal of molecular sciences · 2023
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Forsythiasides: A review of the pharmacological effects.Frontiers in cardiovascular medicine · 2022
    Review
  17. Article
  18. Review
  19. Article
  20. Review
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.

Li DengDepartment of Traditional Chinese Medicine, School of Medicine, Jinan University, Guangzhou 510632, China. dengli@stu2015.jnu.edu.cn.
Peng PangDepartment of Traditional Chinese Medicine, School of Medicine, Jinan University, Guangzhou 510632, China. pangpeng@stu2014.jnu.edu.cn.
Ke ZhengDepartment of Traditional Chinese Medicine, School of Medicine, Jinan University, Guangzhou 510632, China. zhengke@stu2014.jnu.edu.cn.
Jiao NieDepartment of Traditional Chinese Medicine, School of Medicine, Jinan University, Guangzhou 510632, China. 18819351723@163.com.
Huachong XuDepartment of Traditional Chinese Medicine, School of Medicine, Jinan University, Guangzhou 510632, China. xuhuachong@stu2015.jnu.edu.cn.
Sizhi WuDepartment of Traditional Chinese Medicine, School of Medicine, Jinan University, Guangzhou 510632, China. wusizhi@stu2015.jnu.edu.cn.
Jia ChenDepartment of Traditional Chinese Medicine, School of Medicine, Jinan University, Guangzhou 510632, China. fredy212@foxmail.com.
Xiaoyin ChenDepartment of Traditional Chinese Medicine, School of Medicine, Jinan University, Guangzhou 510632, China. tchenxiaoyin@jnu.edu.cn.
Jinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe objective of this study was to observe the effects of forsythoside A on controlling influenza A virus (IAV) infection and improving the prognosis of IAV infection.

methodsForty-eight SPF C57BL/6j mice were randomly divided into the following four groups: Group A: normal control group (normal con); Group B: IAV control group (V con); Group C: IAV+ oseltamivir treatment group (V oseltamivir; 0.78 mg/mL, 0.2 mL/mouse/day); Group D: IAV+ forsythoside A treatment group (V FTA; 2 μg/mL, 0.2 mL/mouse/day). Real-time fluorescence quantitative PCR (RT-qPCR) was used to measure mRNA expression of the TLR7, MyD88, TRAF6, IRAK4 and NF-κB p65 mRNA in TLR7 signaling pathway and the virus replication level in lung. Western blot was used to measure TLR7, MyD88 and NF-κB p65 protein. Flow cytometry was used to detect the proportion of the T cell subsets Th1/Th2 and Th17/Treg.

resultsThe body weight began to decrease after IAV infection, while FTA and oseltamivir could reduce the rate of body weight loss. The pathological damages in the FTA and oseltamivir group were less serious. TLR7, MyD88, TRAF6, IRAK4 and NF-κB p65 mRNA were up-regulated after virus infection (p < 0.01) while down-regulated after oseltamivir and FTA treatment (p < 0.01). The results of TLR7, MyD88 and NF-κB p65 protein consisted with correlative mRNA. Flow cytometry showed the Th1/Th2 differentiated towards Th2, and the Th17/Treg cells differentiated towards Treg after FTA treatment.

conclusionsOur study suggests forsythoside A can control influenza A virus infection and improve the prognosis of IAV infection by inhibiting influenza A virus replication.

Indexed as

AnimalsAntiviral AgentsGene Expression RegulationGlycosidesInfluenza A virusLungMembrane GlycoproteinsMiceMice, Inbred C57BLOrthomyxoviridae InfectionsOseltamivirPrognosisRandom AllocationReal-Time Polymerase Chain ReactionSignal TransductionToll-Like Receptor 7Antiviral AgentsforsythiasideGlycosidesMembrane GlycoproteinsOseltamivirTlr7 protein, mouseToll-Like Receptor 7forsythoside Ainfluenza A virus infectionoseltamivirTLR7 signaling pathway

Identifiers

PMID27128889
PMCPMC6273045
OpenAlexW2343515981

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.