Evidence map›Paper›PMID 42124919›Full record

ArticleTransboundary and emerging diseases2026

Eprinomectin Inhibits

Mengtao Yu, Jiale Guo, Wenqi Liu, Yan Li

Abstract read
In one paragraph

Article in Transboundary and emerging diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Efficient and Stable Subcellular Protein Labeling inPathogens (Basel, Switzerland) · 2026
    Article
  2. Eprinomectin InhibitsTransboundary and emerging diseases · 2026
    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

4 authors.

Mengtao YuDepartment of Pathogen Biology, School of Basic Medicine, Tongji Medical College and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Huazhong University of Science and Technology, Wuhan, 430030, China, hust.edu.cn.ORCID https://orcid.org/0009-0006-3573-425X
Jiale GuoDepartment of Laboratory Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China, hust.edu.cn.ORCID https://orcid.org/0009-0007-4409-217X
Wenqi LiuDepartment of Pathogen Biology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China, hust.edu.cn.ORCID https://orcid.org/0000-0002-3111-4356
Yan LiDepartment of Pathogen Biology, School of Basic Medicine, Tongji Medical College and State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Huazhong University of Science and Technology, Wuhan, 430030, China, hust.edu.cn.ORCID https://orcid.org/0000-0003-1963-839X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Leishmaniasis remains a significant global health challenge, with current therapies often hampered by toxicity, resistance, and high cost. In this study, we investigated the antileishmanial potential of eprinomectin, a veterinary macrocyclic lactone, to address unmet therapeutic needs. Objectives: This study aimed to evaluate the efficacy of eprinomectin against Methods: The antileishmanial activity of eprinomectin was assessed using in vitro and in vivo models. Mechanistic studies included scanning electron microscopy (SEM) to observe morphological changes, transcriptomic profiling to analyze metabolic pathway alterations, and measurements of reactive oxygen species (ROS). Parasite burden and immune responses were further evaluated in infected mice through histopathology and quantitative assays. Results: Eprinomectin exhibited selective activity against Conclusions: Eprinomectin demonstrates multimodal antileishmanial effects primarily through direct parasiticidal mechanisms. Its efficacy in reducing parasite burden and disrupting critical metabolic and cell cycle processes supports its potential as a starting point for antileishmanial drug development. These findings support further investigation into the translational potential of eprinomectin, including combination strategies with existing leishmaniasis treatments.

Indexed as

Antiprotozoal AgentsCell Cycle CheckpointsIvermectinLeishmaniaLeishmaniasisMitochondriaAnimalsFemaleMiceMice, Inbred BALB CAntiprotozoal AgentseprinomectinIvermectincell cycle arresteprinomectinLeishmaniamitochondrial dysfunctionROS

Identifiers

PMID42124919
PMCPMC13158698

What OpenQuestion holds

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LicenceCC BY
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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.