Evidence map›Paper›PMID 33620666›Full record

ArticleApplied biochemistry and biotechnology2021

Pre-treatment with Scopolamine Naturally Suppresses Japanese Encephalitis Viral Load in Embryonated Chick Through Regulation of Multiple Signaling Pathways.

Arghyadeep Bhattacharjee, Rajarshi Chaudhuri, Jiban Jyoti Dash, Manish Saha, Lopamudra Choudhury, Souvik Roy

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Article in Applied biochemistry and biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 11 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

6 authors at 5 institutions in 1 country.

Arghyadeep BhattacharjeeDepartment of Biotechnology, National Institute of Technology Durgapur, Durgapur, West Bengal, India.
Rajarshi ChaudhuriDepartment of Biotechnology, Regional Centre for Biotechnology, Faridabad, Haryana, India.
Jiban Jyoti DashDepartment of Botany, Berhampur University, Berhampur, Odisha, India.
Manish SahaDepartment of Cardiology, R.G Kar Medical College & Hospital, Kolkata, West Bengal, India.
Lopamudra ChoudhuryDepartment of Microbiology, Sarsuna College, Kolkata, West Bengal, India.
Souvik RoyPost-Graduate Department of Biotechnology, St. Xavier's College (Autonomous), Kolkata, West Bengal, India. souvikroybiotech@sxccal.edu.ORCID http://orcid.org/0000-0001-5102-1889
Berhampur University · INNational Institute of Technology Durgapur · INRegional Centre for Biotechnology · INR. G. Kar Medical College and Hospital · INSt Xavier’s College · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Suitable recognition of invasive microorganisms is a crucial factor for evoking a strong immune response that can combat the pathogen. Toll-like receptors (TLRs) play a pivotal role in the induction of this innate immune response through stimulation of interferons (IFNs) that control viral replication in the host via distinct signaling pathways. Though the antiviral property of Atropa belladonna has been established, yet the role of one of its active components scopolamine in modulating various factors of the innate immune branch has not yet been investigated until date. Thus, the present study was conducted to assess the antiviral effects of scopolamine and its immunomodulatory role against Japanese encephalitis virus (JEV) infections in embryonated chick. Pre-treatment with scopolamine hydrobromide showed a significant decrease in the viral loads of chorioallantoic membrane (CAM) and brain tissues. Molecular docking analysis revealed that scopolamine hydrobromide binds to the active site of non-structural protein 5 (NS5) that has enzymatic activities required for replication of JEV, making it a highly promising chemical compound against the virus. The binding contributions of different amino acid residues at or near the active site suggest a potential binding of this compound. Pre-treatment with the scopolamine hydrobromide showed significant upregulation of different TLRs like TLR3, TLR7, and TLR8, interleukins like IL-4, and IL-10, as well as IFNs and their regulatory factors. However, virus-infected tissues (direct infection group) exhibited higher TLR4 expression as compared to scopolamine hydrobromide pre-treated, virus-infected tissues (medicine pre-treated group). These results indicate that scopolamine hydrobromide contributes much to launch antiviral effects by remoulding the TLR and IFN signaling pathways that are involved in sensing and initiating the much-needed anti-JEV responses.

Indexed as

AnimalsAtropa belladonnaAvian ProteinsChick EmbryoEncephalitis, JapaneseEncephalitis Virus, JapaneseScopolamineSignal TransductionAvian ProteinsScopolamineEmbryonated chickInterferonsJapanese encephalitis virusScopolamine hydrobromideSignaling pathwaysToll-like receptors

Identifiers

PMID33620666
OpenAlexW3130769440

What OpenQuestion holds

Textmetadata
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.