Evidence map›Paper›PMID 36064420›Full record

ArticleJournal of orthopaedic surgery and research2022

Resveratrol protection against IL-1β-induced chondrocyte damage via the SIRT1/FOXO1 signaling pathway.

ChuanCai Liang, Hengte Xing, ChenYu Wang, XiongFeng Xu, Yarong Hao, Bo Qiu

Open access · goldAbstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Mechanisms of resveratrol in cartilage injury repair and protection: A review.The Journal of international medical research · 2026
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  4. Article
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  9. Forkhead box O proteins in chondrocyte aging and diseases.Journal of orthopaedic translation · 2025
    Review
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  11. Article
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  14. Article
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  16. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2024
    Article
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  19. 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

6 authors at 2 institutions in 1 country.

ChuanCai LiangDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, China.
Hengte XingDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, China.
ChenYu WangDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, China.
XiongFeng XuDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, China.
Yarong HaoDepartment of Geriatrics, Renmin Hospital of Wuhan University, Wuhan, China. 984022801@qq.cm.
Bo QiuDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, China. qbtg163@163.com.
Wuhan University · CNRenmin Hospital of Wuhan University · CN

Funding

National Natural Science Foundation of China 81071494Science and Technology Department of Hubei Province 2015BCA316
6 · The paper itself

Abstract

purposeOsteoarthritis (OA) is a common joint disease characterized by cartilage degeneration, synovial inflammation, osteophytes, and subchondral osteosclerosis. This study investigated the effects of resveratrol (RES) on extracellular matrix (ECM), autophagy, and apoptosis in OA pathogenesis via the SIRT1/FOXO1 pathway.

methodsThe microenvironment of OA chondrocytes was stimulated in vitro by adding 10 ng/mL of IL-1β to primary Wistar rat chondrocyte. Western blotting, immunofluorescence, quantitative real-time PCR, and transmission electron microscopy (TEM) were used for analysis.

resultsIn the presence of IL-1β, RES increased the expression of silent information regulator (SIR) 1 protein and the phosphorylation level of forkhead transcription factor (FOXO) 1. It also promoted chondrocyte autophagy, increased the expression of SOX9 and aggrecan, inhibited chondrocyte apoptosis and matrix breakdown, and protected chondrocytes from IL-1β damage. After a SIRT1 inhibitor or FOXO1 inhibitor was added, the protective effect of RES on chondrocytes was significantly weakened. Our results suggest that RES regulates the ECM metabolism, autophagy, and apoptosis of OA chondrocytes through the SIRT1/FOXO1 pathway to ameliorate IL-1β-induced chondrocyte injury.

conclusionRES protects chondrocytes from IL-1β-induced damage by activating SIRT1/FOXO1 signaling and holds potential in OA treatment.

Indexed as

ChondrocytesOsteoarthritisAnimalsForkhead Box Protein O1Interleukin-1betaNerve Tissue ProteinsRatsRats, WistarResveratrolSignal TransductionSirtuin 1Forkhead Box Protein O1Foxo1 protein, ratInterleukin-1betaNerve Tissue ProteinsResveratrolSirt1 protein, ratSirtuin 1ApoptosisAutophagyChondrocytesExtracellular matrixOsteoarthritisResveratrol

Identifiers

PMID36064420
PMCPMC9446849
OpenAlexW4294647504

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.