Evidence map›Paper›PMID 31737218›Full record

ArticleAmerican journal of translational research2019

Rutin suppresses FNDC1 expression in bone marrow mesenchymal stem cells to inhibit postmenopausal osteoporosis.

Yuhong Xiao, Ran Wei, Zhen Yuan, Xiaoyong Lan, Jin Kuang, Dongxia Hu, Yi Song, Jun Luo

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

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  18. Preventive Effects ofEvidence-based complementary and alternative medicine : eCAM · 2020
    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.

Yuhong XiaoDepartment of Rehabilitation Medicine, The Second Affiliated Hospital of Nanchang University Nanchang 330006, Jiangxi, China.
Ran WeiDepartment of General Surgery, The Second Affiliated Hospital of Nanchang University Nanchang 330006, Jiangxi, China.
Zhen YuanDepartment of Rehabilitation Medicine, The Second Affiliated Hospital of Nanchang University Nanchang 330006, Jiangxi, China.
Xiaoyong LanDepartment of Rehabilitation Medicine, The Second Affiliated Hospital of Nanchang University Nanchang 330006, Jiangxi, China.
Jin KuangDepartment of General Surgery, The Second Affiliated Hospital of Nanchang University Nanchang 330006, Jiangxi, China.
Dongxia HuDepartment of Rehabilitation Medicine, The Second Affiliated Hospital of Nanchang University Nanchang 330006, Jiangxi, China.
Yi SongDepartment of General Surgery, The Second Affiliated Hospital of Nanchang University Nanchang 330006, Jiangxi, China.
Jun LuoDepartment of Rehabilitation Medicine, The Second Affiliated Hospital of Nanchang University Nanchang 330006, Jiangxi, China.
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A previous study revealed that rutin is the main component of Eucommia flavonoids that exerts a protective effect against osteopenia. The bone density and trabecular bone number of osteoporosis model rats can be significantly improved after treatment with rutin. Further study using whole gene expression profiling revealed that FNDC1, a fibronectin type III domain-containing protein, may be a novel bone metabolism-related factor that is decreased in rutin-treated rats. The mechanism underlying the effects of rutin treatment on osteoporosis is important to explore. Micro-CT, western blotting, quantitative PCR, transmission electron microscopy, and Alizarin Red mineralization staining assays were performed to evaluate bone density, FNDC1 expression and autophagy to determine whether FNDC1 might play a significant role in rutin-inhibited trabecular bone loss in rats. FNDC1 expression was high in the osteoporosis group, whereas rutin treatment facilitated FNDC1 downregulation. In addition, rutin promoted bone marrow mesenchymal stem cell autophagy by inhibiting phosphorylated Akt in osteoporosis. In summary, our study shows that rutin could regulate FNCD1 level and autophagy through the Akt/mTOR signaling pathway to provide a novel therapeutic strategy for osteoporosis.

Indexed as

autophagyFNDC1postmenopausal osteoporosisRutin

Identifiers

PMID31737218
PMCPMC6834492
OpenAlexW2995249747

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.