Evidence map›Paper›PMID 36573068›Full record

ArticleDrug design, development and therapy2022

Antiviral Activity of Oridonin Against Herpes Simplex Virus Type 1.

Kai Jiang, Jing Feng, Xia Qi, Lili Ran, Lixin Xie

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Cell death network regulation in HSV infection: immune evasion versus host defense.Apoptosis : an international journal on programmed cell death · 2026
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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 2 institutions in 1 country.

Kai JiangDepartment of Ophthalmology, the Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, People's Republic of China.
Jing FengEye Institute of Shandong First Medical University, Eye Hospital of Shandong First Medical University, Qingdao, People's Republic of China.
Xia QiEye Institute of Shandong First Medical University, Eye Hospital of Shandong First Medical University, Qingdao, People's Republic of China.
Lili RanEye Institute of Shandong First Medical University, Eye Hospital of Shandong First Medical University, Qingdao, People's Republic of China.ORCID 0000-0003-0429-175X
Lixin XieEye Institute of Shandong First Medical University, Eye Hospital of Shandong First Medical University, Qingdao, People's Republic of China.
Shandong Eye Hospital · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: In search of new potent treatment of herpes simplex keratitis (HSK), inhibitory effect of oridonin (Ori) on herpes simplex virus type 1 (HSV-1) was validated by experiments. Methods: For evaluating inhibitory effect of oridonin on herpes simplex virus type 1, a series of in-vivo and in-vitro studies were carried out. Mouse HSV-1 infection model was used in the in-vivo experiments. Experimental mice were classified in five different groups: Mock (mock-infected), HSV-1+ DMSO, HSV-1+ Ori, HSV-1+ ACV, combined Ori and ACV+HSV-1. Corneas of Mock, HSV-1+ DMSO, HSV-1+ Ori group were sent for mRNA-sequencing after 3 days post infection (dpi). The expression of virus and host-related genes was evaluated by quantitative real-time polymerase chain reaction (qPCR). Vero cells HSV-1 infection models were used in the in-vitro experiments. Results: The application of ACV, Oridonin alone or a combination of both could alleviate HSV-1 severity and inhibit HSV-1 virus replication in C57BL/6 mice models. qPCR showed that compared with mock group, the expression of Conclusion: Oridonin alleviates herpes simplex keratitis infection in mouse, which may be attributed to inhibition of the NLRP3-inflammasome-IL-1β pathway. Our study illustrates that Oridonin has potential promise for application in treating HSK and other diseases caused by HSV-1 infection.

Indexed as

Herpes SimplexHerpesvirus 1, HumanKeratitis, HerpeticAnimalsAntiviral AgentsChlorocebus aethiopsDimethyl SulfoxideDiterpenes, KauraneMiceMice, Inbred C57BLNLR Family, Pyrin Domain-Containing 3 ProteinVero CellsAntiviral AgentsDimethyl SulfoxideDiterpenes, KauraneNLR Family, Pyrin Domain-Containing 3 Proteinoridoninherbherpes simplex keratitisHSV-1inflammasomenlrp3oridonin

Identifiers

PMID36573068
PMCPMC9789684
OpenAlexW4312079293

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.