Evidence map›Paper›PMID 39599879›Full record

ArticleViruses2024

Protective Role of Cepharanthine Against Equid Herpesvirus Type 8 Through AMPK and Nrf2/HO-1 Pathway Activation.

Shuwen Li, Liangliang Li, Yijia Sun, Muhammad Zahoor Khan, Yue Yu, Lian Ruan, Li Chen, Juan Zhao, Junchi Jia, Yubao Li and 2 more

Abstract read
In one paragraph

Article in Viruses, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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

12 authors.

Shuwen LiCollege of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, China.
Liangliang LiCollege of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, China.ORCID 0000-0001-5431-9103
Yijia SunCollege of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, China.
Muhammad Zahoor KhanCollege of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, China.ORCID 0000-0001-5890-2996
Yue YuCollege of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, China.
Lian RuanCollege of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, China.
Li ChenCollege of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, China.
Juan ZhaoCollege of Veterinary Medicine, Shanxi Agricultural University, Taigu, Jinzhong 030801, China.
Junchi JiaCollege of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, China.
Yubao LiCollege of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, China.
Changfa WangCollege of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, China.
Tongtong WangCollege of Agricultural Science and Engineering, Liaocheng University, Liaocheng 252000, China.

Funding

National Key R&D Program of China 2022YFD1600103;2023YFD1302004
6 · The paper itself

Abstract

Equid herpesvirus type 8 (EqHV-8) is known to cause respiratory disease and miscarriage in horses and donkeys, which is a major problem for the equine farming industry. However, there are currently limited vaccines or drugs available to effectively treat EqHV-8 infection. Therefore, it is crucial to develop new antiviral approaches to prevent potential pandemics caused by EqHV-8. This study evaluates the antiviral and antioxidant effects of cepharanthine against EqHV-8 by employing both in vitro assays and in vivo mouse models to assess its therapeutic efficacy. To assess the effectiveness of cepharanthine against EqHV-8, we conducted experiments using NBL-6 and RK-13 cells. Additionally, we developed a mouse model to validate cepharanthine's effectiveness against EqHV-8. In our in vitro experiments, we assessed the cepharanthine's ability to inhibit infection caused by EqHV-8 in NBL-6 and RK-13 cells. Our results demonstrated that cepharanthine has a dose-dependent inhibitory effect, indicating that it possesses anti-EqHV-8 properties at the cellular level. Moreover, we investigated the mechanism through which cepharanthine exerts its protective effects. It was observed that cepharanthine effectively reduces the oxidative stress induced by EqHV-8 by activating the AMPK and Nrf2/HO-1 signaling pathways. Furthermore, when administered to EqHV-8 infected mice, cepharanthine significantly improved lung tissue pathology and reduced oxidative stress. The findings presented herein collectively highlight cepharanthine as a promising candidate for combating EqHV-8 infections.

Indexed as

Antiviral AgentsBenzylisoquinolinesHerpesviridae InfectionsNF-E2-Related Factor 2AMP-Activated Protein KinasesAnimalsBenzodioxolesCell LineDisease Models, AnimalEquidaeFemaleHeme Oxygenase-1HerpesviridaeHorsesMiceSignal TransductionAMP-Activated Protein KinasesAntiviral AgentsBenzodioxolesBenzylisoquinolinescepharanthineHeme Oxygenase-1Nfe2l2 protein, mouseNF-E2-Related Factor 2AMPK/Nrf2/HO-1 signaling pathwayantiviral activitycepharanthineEqHV-8oxidative stress

Identifiers

PMID39599879
PMCPMC11598968

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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.