Evidence map›Paper›PMID 42909281›Full record

ArticleFrontiers in pharmacology2026

Isoalantolactone exhibits activity against

Wei Ma, Chuanchuan Liu, Haining Fan

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Wei MaDepartment of Cardiovascular Surgery, Qinghai University Affiliated Hospital (Clinical Medical College), Xining, Qinghai Province, China.
Chuanchuan LiuCentral Laboratory, Qinghai University Affiliated Hospital (Clinical Medical College), Xining, Qinghai Province, China.
Haining FanGeneral Surgery, Qinghai University Affiliated Hospital (Clinical Medical College), Xining, Qinghai Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Alveolar echinococcosis (AE) is a severe parasitic disease caused by Methods: Results: ISO promoted phosphoglucose isomerase release, with a half-maximal effective concentration of 16.36 ± 3.24 μM, and reduced germinal cell viability, with a half-maximal inhibitory concentration of 17.46 ± 2.25 μM. It exerted dose- and time-dependent parasiticidal effects, achieving complete protoscolex death within 1-5 days at concentrations of 40 μM and 10 μM, respectively. In infected mice, ISO reduced lesion burden and spleen index and was associated with parasite structural damage, mitochondrial abnormalities, and changes in fibrosis-, inflammation-, and immune-related readouts under the present experimental conditions, with no marked abnormalities in most of the evaluated short-term safety parameters. Conclusion: ISO shows anti-

Indexed as

alveolar echinococcosisantiparasitic therapyEchinococcus multilocularishost immune responseisoalantolactonelesion microenvironmentmitochondrial perturbationnatural products

Identifiers

PMID42909281
PMCPMC13684005

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.