Evidence map›Paper›PMID 42395015›Full record

ArticleJournal of ginseng research2026

20(S)-protopanaxatriol alleviates gastritis by attenuating oxidative stress and inflammatory responses via inhibition of PI3K/AKT and JAK/STAT3 pathways.

Yuhao Wang, Jae Youl Cho, Daewon Kim

Abstract read
In one paragraph

Article in Journal of ginseng research, 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.

Yuhao WangDepartment of Integrative Biotechnology, and Biomedical Institute for Convergence at SKKU, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Jae Youl ChoDepartment of Integrative Biotechnology, and Biomedical Institute for Convergence at SKKU, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Daewon KimComposite & Fusion Media Processing Lab., Department of Computer Engineering, Dankook University, Yongin, 16890, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Inflammation is a fundamental protective response of the body; however, chronic or excessive inflammation can perturb immune homeostasis and elevate the risk of cardiovascular, metabolic, and oncological diseases. Protopanaxatriol (PPT), a principal bioactive metabolite of Purpose: This study aims to evaluate the anti-inflammatory potential of PPT and elucidate mechanistic pathways. Methods: Potential targets and signaling pathways were predicted using Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment. The anti-inflammatory activity of PPT was assessed Results: PPT markedly attenuated LPS-induced inflammatory responses at non-cytotoxic concentrations, suppressing NO production and reducing expression of interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β). Conclusion: PPT exerts potent anti-inflammatory effects by inhibiting PI3K/AKT and JAK-STAT3 signaling and alleviating oxidative stress. These findings support PPT as a promising candidate for the development of novel anti-inflammatory therapeutics.

Indexed as

Anti-inflammationGastritisGinsenosidesProtopanaxatriol

Identifiers

PMID42395015
PMCPMC13324098

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.