Evidence map›Paper›PMID 34836523›Full record

ArticleBMC complementary medicine and therapies2021

Arctiin suppresses H9N2 avian influenza virus-mediated inflammation via activation of Nrf2/HO-1 signaling.

Beixian Zhou, Linxin Wang, Yueyun Liang, Jing Li, Xiping Pan

Open access · goldAbstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
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

12 citing papers in PubMed, 27 citations in OpenAlex.

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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

5 authors at 3 institutions in 1 country.

Beixian Zhou *Center of stem cell and Regenerative Medicine, The People's Hospital of Gaozhou, Gaozhou, China.
Linxin Wang *Guangzhou Laboratory, No. 9, XingDaoHuanBei Road, Guangzhou International Bio Island, Guangzhou, 510005, China.
Yueyun LiangDepartment of Anesthesiology, The People's Hospital of Gaozhou, Gaozhou, China.
Jing LiState Key Laboratory of Respiratory Disease, National Clinical Research Center of Respiratory Disease, Guangzhou Institute of Respiratory Health, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, NO. 195, Dongfengxi Road, Guangzhou, 510120, China. lijinghenan@163.com.
Xiping PanGuangzhou Laboratory, No. 9, XingDaoHuanBei Road, Guangzhou International Bio Island, Guangzhou, 510005, China. xppan116@sina.com.
Gaozhou People's Hospital · CNGuangzhou Experimental Station · CNFirst Affiliated Hospital of Guangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundH9N2 avian influenza viruses (AIVs) infect avian and mammalian hosts and provide internal genes for new emerging highly pathogenic avian viruses that cause severe pneumonia with high mortality, for which few medications are available. Arctiin, a bioactive lignan glycoside, has been reported to possess multiple pharmacological properties. However, the effect of arctiin on H9N2 virus infection is unclear. In the current study, we analyzed the effect of arctiin on H9N2 virus infection and the underlying molecular mechanism in vitro.

methodsThe antiviral effect against H9N2 virus was determined by plaque reduction assay (PRA) and progeny virus reduction assay. We employed MTT assay, qRT-PCR, ELISA, immunofluorescence and Western blotting to better understand the anti-inflammatory effect and corresponding mechanism of arctiin on H9N2 virus-infected cells.

resultsThe results showed that arctiin had antiviral activity against H9N2 virus. Arctiin treatment reduced H9N2 virus-triggered proinflammatory cytokines, such as IL-6, and TNF-α. Moreover, arctiin significantly suppressed H9N2 virus-mediated expression of COX-2 and PGE

conclusionTaken together, these results suggested that the anti-inflammatory effects of arctiin on H9N2 virus infection may be due to the activation of Nrf2/HO-1 and blocked RIG-I/JNK MAPK signaling; thus, arctiin may be a promising agent for prevention and treatment of H9N2 virus infections.

Indexed as

A549 CellsAnimalsAnti-Inflammatory AgentsChinaDogsFuransGlucosidesHeme Oxygenase-1HumansInfluenza A Virus, H9N2 SubtypeMadin Darby Canine Kidney CellsMolecular StructureNF-E2-Related Factor 2Plant ExtractsAnti-Inflammatory AgentsarctiinFuransGlucosidesHeme Oxygenase-1HMOX1 protein, humanNFE2L2 protein, humanNF-E2-Related Factor 2Plant Extractsanti-inflammatoryarctiinArctium lappa L.H9N2 avian influenza viruslignan

Identifiers

PMID34836523
PMCPMC8620712
OpenAlexW3189441855

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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.