Evidence map›Paper›PMID 27803787›Full record

ArticleIranian journal of basic medical sciences2016

Anti-inflammatory effect of Yu-Ping-Feng-San

Zhong-Shan Yang, Jin-Yuan Yan, Ni-Ping Han, Wei Zhou, Yu Cheng, Xiao-Mei Zhang, Ning Li, Jia-Li Yuan

Open access · greenAbstract read
In one paragraph

Article in Iranian journal of basic medical sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

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  11. Curcumin and Curcumol Inhibit NF-Evidence-based complementary and alternative medicine : eCAM · 2019
    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

8 authors at 2 institutions in 1 country.

Zhong-Shan YangFaculty of Basic Medical Science, Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan.
Jin-Yuan YanCentral laboratory, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan.
Ni-Ping HanFaculty of Basic Medical Science, Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan.
Wei ZhouFaculty of Basic Medical Science, Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan.
Yu ChengFaculty of Basic Medical Science, Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan.
Xiao-Mei ZhangFaculty of Basic Medical Science, Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan.
Ning LiFaculty of Basic Medical Science, Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan.
Jia-Li YuanFaculty of Basic Medical Science, Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan.
Yunnan University of Traditional Chinese Medicine · CNKunming Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesYu-Ping-Feng-San (YPFS) is a classical traditional Chinese medicine that is widely used for treatment of the diseases in respiratory systems, including chronic obstructive pulmonary disease (COPD) recognized as chronic inflammatory disease. However, the molecular mechanism remains unclear. Here we detected the factors involved in transforming growth factor beta 1 (TGF-β1)/Smad2 signaling pathway and inflammatory cytokines, to clarify whether YPFS could attenuate inflammatory response dependent on TGF-β1/Smad2 signaling in COPD rats or cigarette smoke extract (CSE)-treated human bronchial epithelial (Beas-2B) cells. MATERIALS AND

methodsThe COPD rat model was established by exposure to cigarette smoke and intratracheal instillation of lipopolysaccharide, YPFS was administered to the animals. The efficacy of YPFS was evaluated by comparing the severity of pulmonary pathological damage, pro-inflammation cytokines, collagen related genes and the activation of TGF-β1/Smad2 signaling pathway. Furthermore, CSE-treated cells were employed to confirm whether the effect of YPFS was dependent on the TGF-β1/Smad2 signaling via knockdown Smad2 (Si-RNA), or pretreatment with the inhibitor of TGF-β1.

resultsAdministration of YPFS effectively alleviated injury of lung, suppressed releasing of pro-inflammatory cytokines and collagen deposition in COPD animals (

conclusionYPFS accomplished anti-inflammatory effects mainly by suppressing phosphorylation of Smad2, TGF-β1/Smad2 signaling pathway was required for YPFS-mediated anti-inflammation in COPD rats or CSE-treated Beas-2B cells.

Indexed as

COPDCytokinePro-inflammatoryTGF-β1/Smad2YPFS

Identifiers

PMID27803787
PMCPMC5080430
OpenAlexW2526649676

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.