Evidence map›Paper›PMID 42711652›Full record

ArticleCell biochemistry and biophysics2026

Vestitol Ameliorates Ferroptosis-Associated Features and Osteoarthritis Progression Through Modulation of the GSK3B/Nrf2/GPX4 Pathway.

Tingting Wang, Yongxiang Liu

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

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

2 authors.

Tingting WangDepartment of Orthopedics, Yantaishan Hospital, No.10087, Kejidadao, Laishan District, Yantai, 264003, Shandong, China.
Yongxiang LiuDepartment of Orthopedics, Yantaishan Hospital, No.10087, Kejidadao, Laishan District, Yantai, 264003, Shandong, China. 18704688285@163.com.ORCID http://orcid.org/0009-0005-4689-8703

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to investigate whether vestitol ameliorates osteoarthritis (OA) and the mechanisms involved. We employed destabilization of the medial meniscus (DMM)-constructed OA mouse model and IL-1β-induced chondrocyte model to evaluate vestitol's effects on OA. In vivo, pathological alterations in cartilage tissues were assessed via safranin O and H&E staining. In vitro, chondrocyte viability and apoptosis were detected utilizing CCK-8 and flow cytometry. Vestitol's mechanisms in OA were explored using network pharmacology analysis. Factors related to extracellular matrix (ECM) degeneration, inflammation, oxidative stress, ferroptosis, and pathway were checked using western blot, RT-qPCR, immunohistochemistry, and corresponding commercial reagent kits. In OA mice model, vestitol decreased cartilage destruction and OARSI score. Vestitol enhanced the levels of COL2A1, Aggrecan, SOD, FTH1, but reduced the levels of MMP-13, ADAMTS5, IL-6, IL-1β, COX-2, TNF-α, MDA, Fe

Indexed as

FerroptosisGSK3B/Nrf2/GPX4 pathwayInflammationOsteoarthritisVestitol

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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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 Socratic graph.