Evidence map›Paper›PMID 30796639›Full record

ArticleMolecular diversity2020

Lupenone is a good anti-inflammatory compound based on the network pharmacology.

Feng Xu, Liubo Yang, Xulong Huang, Yuqing Liang, Xiangpei Wang, Hongmei Wu

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular diversity, 2020. 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
1.1field-weighted citation impact, top 23% 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, 35 citations in OpenAlex.

  1. Analysis of Quality Differences inFood science & nutrition · 2026
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  6. PeerJ · 2024
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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

6 authors at 2 institutions in 1 country.

Feng XuCollege of Pharmacy, Guiyang University of Chinese Medicine, Guiyang, People's Republic of China.
Liubo YangCollege of Pharmacy, Guiyang University of Chinese Medicine, Guiyang, People's Republic of China.
Xulong HuangCollege of Pharmacy, Guiyang University of Chinese Medicine, Guiyang, People's Republic of China.
Yuqing LiangCollege of Pharmacy, Guiyang University of Chinese Medicine, Guiyang, People's Republic of China.
Xiangpei WangCollege of Pharmacy, Guiyang University of Chinese Medicine, Guiyang, People's Republic of China.
Hongmei WuExperiment Center, Guiyang University of Chinese Medicine, 50, Nanming District, Guiyang, 550002, Guizhou Province, People's Republic of China. whm0425@126.com.ORCID http://orcid.org/0000-0002-4974-0785
Guiyang University · CNGuiyang College of Traditional Chinese Medicine · CN

Funding

Guiyang Univerisity of Chinese Medicine Doctor Startup Fund 2017Guizhou Province Science and Technology Project QiankeheLHzi [2016] 7116National Natural Science Foundation of China 81860737The Guizhou Domestic First-class Construction Project [(Chinese Materia Medica) GNYL [2017] 008)
6 · The paper itself

Abstract

The dried rhizome of Musa basjoo Sieb. et Zucc. is Rhizoma Musae. It has been used to treat diabetes in Miao medicine in China. Lupenone was isolated from Rhizoma Musae and has good anti-diabetic activity. Its mechanism of action is unclear. Diabetes is a chronic low-level systemic inflammatory disease, and lupenone has anti-inflammatory activity, but the underlying mechanism is not fully elucidated. In this study, we aimed to construct the drug-target biologic network and predict the anti-inflammatory mechanism of lupenone. The network-based pharmacologic analysis platform was used to identify the target proteins related to inflammation. Furthermore, the effects of lupenone on acute, subacute and diabetic pancreatic inflammation were evaluated. The "component-target-disease" network was constructed using Cytoscape. Lupenone could regulate transcription factor p65, NF-kappa-B inhibitor alpha, transcription factor AP-1, NF-kappa-B essential modulator, nuclear factor NF-kappa-B p105 subunit, epidermal growth factor receptor, hypoxia-inducible factor 1-alpha and other proteins related to the PI3K-Akt, Toll-like receptor and NF-kappa B signaling pathways. In addition, lupenone significantly decreased acute and subacute inflammation in mice as well as the IL-1β and IFN-γ levels in the pancreas of diabetic rats. The above results provide strong support for studying the molecular mechanism of lupenone in the treatment of diabetes from the perspective of anti-inflammation.

Indexed as

Computational BiologyAnimalsAnti-Inflammatory AgentsCarrier ProteinsCytokinesDisease Models, AnimalEdemaInflammation MediatorsLupanesMaleMiceModels, MolecularProtein BindingRatsStructure-Activity RelationshipTechnology, PharmaceuticalAnti-Inflammatory AgentsCarrier ProteinsCytokinesInflammation MediatorsLupaneslupenoneTriterpenesDiabetesInflammationLupenoneNetwork pharmacologyPancreasTarget

Identifiers

PMID30796639
OpenAlexW2915190202

What OpenQuestion holds

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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.