Evidence map›Paper›PMID 35451724›Full record

ArticleInflammopharmacology2022

Yangonin treats inflammatory osteoporosis by inhibiting the secretion of inflammatory factors and RANKL expression.

Feng Lu, Xinhui Wu, Huiqun Hu, Jiapeng Zhang, Xiaoting Song, Xiangang Jin, Lihua Chen, Jiacheng Sun, Haixiao Chen

Abstract read
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In one paragraph

Article in Inflammopharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Aging · 2024
    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

9 authors at 2 institutions in 1 country.

Feng LuZhejiang University School of Medicine, Hangzhou, 310009, China.
Xinhui WuWenzhou Medical University, Wenzhou, 325035, China.
Huiqun HuZhejiang University School of Medicine, Hangzhou, 310009, China.
Jiapeng ZhangWenzhou Medical University, Wenzhou, 325035, China.
Xiaoting SongWenzhou Medical University, Wenzhou, 325035, China.
Xiangang JinZhejiang University School of Medicine, Hangzhou, 310009, China.
Lihua ChenEnze Medical Research Center, Taizhou Hospital Affiliated to Wenzhou Medical University, Linhai, 317000, China.
Jiacheng SunWenzhou Medical University, Wenzhou, 325035, China.
Haixiao ChenZhejiang University School of Medicine, Hangzhou, 310009, China. xs_luf@enzemed.com.ORCID http://orcid.org/0000-0002-6178-0974
Wenzhou Medical University · CNSecond Affiliated Hospital of Zhejiang University · CN

Funding

Natural Science Foundation of Zhejiang Province LY20H060006
6 · The paper itself

Abstract

objectivesAs the main cause of osteoporosis, abnormal activity of osteoclasts could disrupt the balance between bone resorption and formation. Moreover, up-regulation of nuclear factor-kappa ligand (RANKL) expression by chronic inflammation-mediated inflammatory factors might contribute to the differentiation of osteoclast precursor cells. Therefore, an anti-inflammatory agent named yangonin was presented for inhibiting osteoclast and relieving inflammatory osteoporosis through down-regulating inflammatory factors.

methodsWe established a model of macrophage inflammation and then verified the anti-inflammatory effect of yangonin. The inhibitory effect of yangonin on osteoclasts was detected by tartrate-resistant acid phosphatase (TRAP) staining, Western blotting and quantitative real-time PCR (qRT-PCR). Finally, micro-CT, TRAP and hematoxylin-eosin (HE) staining were used to show the effect of yangonin on inflammatory osteoporosis in vivo.

resultsOur results suggested that yangonin was able to reduce the secretion of inflammatory factors, down-regulate osteoclast-related genes such as TRAP, RANKL, cathepsin K (CTSK) and nuclear factor-activated T-cell 1 (NFATc1). Furthermore, it was demonstrated that yangonin could suppress the function of inflammatory cytokines in osteoclast differentiation and reporting, wherein NF-κB, AKT and downstream c-Fos/NFATc1 signaling pathways were involved. In an in vivo study, we implied that yangonin has a relieving effect on inflammatory osteoporosis.

conclusionOur research shows that yangonin down-regulates inflammatory factors and inhibits the bone-breaking effect of inflammation through NF-κB, AKT and downstream c-Fos/NFATc1 signaling pathways to achieve the purpose of treating inflammatory osteoporosis.

Indexed as

Bone ResorptionOsteoporosisCell DifferentiationHumansInflammationLigandsNF-kappa BOsteoclastsProto-Oncogene Proteins c-aktPyronesRANK LigandLigandsNF-kappa BProto-Oncogene Proteins c-aktPyronesRANK LigandyangoninChronic inflammationLPSOsteoclastsOsteoporosisRANKLYangonin

Identifiers

PMID35451724
OpenAlexW4224233644

What OpenQuestion holds

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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.