Evidence map›Paper›PMID 30662673›Full record

ArticleAmerican journal of translational research2018

Quercetin rescued TNF-alpha-induced impairments in bone marrow-derived mesenchymal stem cell osteogenesis and improved osteoporosis in rats.

Zhen Yuan, Jun Min, Yawen Zhao, Qingfeng Cheng, Kai Wang, Sijian Lin, Jun Luo, Hao Liu

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.0field-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

47 citing papers in PubMed, 74 citations in OpenAlex.

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  17. Oxidative medicine and cellular longevity · 2023
    Article
  18. ATP-induced cell death: a novel hypothesis for osteoporosis.Frontiers in cell and developmental biology · 2023
    Review
  19. Frontiers in medicine · 2023
    Review
  20. 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

8 authors at 1 institution in 1 country.

Zhen YuanDepartment of Rehabilitation, The Second Affiliated Hospital of Nanchang University Nanchang, Jiangxi, People's Republic of China.
Jun MinDepartment of Rehabilitation, The Third Affiliated Hospital of Nanchang University Nanchang, Jiangxi, People's Republic of China.
Yawen ZhaoDepartment of Rehabilitation, The Second Affiliated Hospital of Nanchang University Nanchang, Jiangxi, People's Republic of China.
Qingfeng ChengDepartment of Rehabilitation, The Second Affiliated Hospital of Nanchang University Nanchang, Jiangxi, People's Republic of China.
Kai WangDepartment of Rehabilitation, The Second Affiliated Hospital of Nanchang University Nanchang, Jiangxi, People's Republic of China.
Sijian LinDepartment of Rehabilitation, The Second Affiliated Hospital of Nanchang University Nanchang, Jiangxi, People's Republic of China.
Jun LuoDepartment of Rehabilitation, The Second Affiliated Hospital of Nanchang University Nanchang, Jiangxi, People's Republic of China.
Hao LiuDepartment of Rehabilitation, The Second Affiliated Hospital of Nanchang University Nanchang, Jiangxi, People's Republic of China.
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the effect of quercetin on promoting the proliferation of bone marrow mesenchymal stem cells (BMSCs) and improving osteoporosis in rats. Rats were randomly divided into the sham, OVX and quercetin+OVX groups. In the sham and OVX groups, rats were given carboxymethyl cellulose sodium (CMC-Na). In the quercetin+OVX group, rats were given quercetin (50 mg/kg) once a day. Eight weeks after rats were treated, femurs were subjected to micro-CT scans, and bone biomechanical properties were analysed by the three-point flexural test. In addition, BMSCs were isolated and characterised by MTT, RT-PCR and Western blot analysis. In vivo, quercetin increased bone mineral density (BMD) and improved bone biomechanical properties in postmenopausal osteoporosis rat models. In vitro, TNF-α led to the activation of nuclear factor-kappa B (NF-κB) and the degradation of β-catenin, which were significantly inhibited by quercetin. Furthermore, quercetin promoted BMSC proliferation and osteogenic differentiation. In conclusion, quercetin improved in vitro models of osteoporosis and protected against TNF-α-induced impairments in BMSC osteogenesis.

Indexed as

BMSCsosteoporosisQuercetinTNF-α

Identifiers

PMID30662673
PMCPMC6325508
OpenAlexW2989483464

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.