Evidence map›Paper›PMID 27041460›Full record

ArticleActa pharmacologica Sinica2016

Hyperoside exerts anti-inflammatory and anti-arthritic effects in LPS-stimulated human fibroblast-like synoviocytes in vitro and in mice with collagen-induced arthritis.

Xiang-Nan Jin, En-Zhi Yan, Han-Ming Wang, Hai-Juan Sui, Zhou Liu, Wei Gao, Ying Jin

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
6.9field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 84 citations in OpenAlex.

  1. Pooled it
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  6. ACS omega · 2025
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  8. Effects and molecular mechanisms ofFrontiers in pharmacology · 2025
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  13. Frontiers in chemistry · 2022
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  15. Article
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  18. Article
  19. Molecules (Basel, Switzerland) · 2020
    Article
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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

7 authors at 1 institution in 1 country.

Xiang-Nan JinDepartment of Rheumatoid Immunity, the First Affiliated Hospital.
En-Zhi YanDepartment of Pharmacology, Liaoning Medical University, Jinzhou 121001, China.
Han-Ming WangDepartment of Pharmacology, Liaoning Medical University, Jinzhou 121001, China.
Hai-Juan SuiDepartment of Pharmacology, Liaoning Medical University, Jinzhou 121001, China.
Zhou LiuDepartment of Pharmacology, Liaoning Medical University, Jinzhou 121001, China.
Wei GaoDepartment of Rheumatoid Immunity, the First Affiliated Hospital.
Ying JinDepartment of Pharmacology, Liaoning Medical University, Jinzhou 121001, China.
Jinzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimHyperoside is a flavonol glycoside mainly found in plants of the genera Hypericum and Crataegus, which has shown anti-oxidant, anti-cancer and anti-inflammatory activities. In this study, we investigated the effects of hyperoside on human rheumatoid fibroblast-like synoviocytes (FLSs) in vitro and on mouse collagen-induced arthritis (CIA) in vivo.

methodsFLSs were isolated from primary synovial tissues obtained from rheumatoid arthritis (RA) patients and exposed to LPS (1 μg/mL). Cell viability and proliferation were measured with MTT and BrdU assay. Cell migration was assessed using wound-healing assay and Transwell assay. DNA binding of NF-κB was measured using a TransAM-NFkappaB kit. The localization of p65 subunit was detected with immunocytochemistry. CIA was induced in mice by primary immunization with Bovine Type II collagen (CII) emulsified in CFA, followed by a booster injection 3 weeks later. The arthritic mice were treated with hyperoside (25, 50 mg·kg(-1)·d(-1), ip) for 3 weeks, and the joint tissues were harvested for histological analysis.

resultsHyperoside (10, 50, 100 μmol/L) dose-dependently inhibited LPS-induced proliferation and migration of human RA FLSs in vitro. Furthermore, hyperoside decreased LPS-stimulated production of TNF-α, IL-6, IL-1 and MMP-9 in the cells. Moreover, hyperoside inhibited LPS-induced phosphorylation of p65 and IκBα, and suppressed LPS-induced nuclear translocation of p65 and DNA biding of NF-κB in the cells. Three-week administration of hyperoside significantly decreased the clinical scores, and alleviated synovial hyperplasia, inflammatory cell infiltration and cartilage damage in mice with CIA.

conclusionHyperoside inhibits LPS-induced proliferation, migration and inflammatory responses in human RA FLSs in vitro by suppressing activation of the NF-κB signaling pathway, which contributes to the therapeutic effects observed in mice with CIA.

Indexed as

AnimalsAnti-Inflammatory AgentsAntirheumatic AgentsArthritis, ExperimentalArthritis, RheumatoidBone and BonesCell MovementCell ProliferationCells, CulturedCollagenCytokinesHumansLipopolysaccharidesMaleMice, Inbred DBANF-kappa BAnti-Inflammatory AgentsAntirheumatic AgentsCollagenCytokineshyperosideLipopolysaccharidesNF-kappa BNF-KappaB Inhibitor alphaQuercetin

Identifiers

PMID27041460
PMCPMC4857551
OpenAlexW2339275816

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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 OpenQuestion graph.