Evidence map›Paper›PMID 34583676›Full record

ArticleBMC complementary medicine and therapies2021

Myrtenal and β-caryophyllene oxide screened from Liquidambaris Fructus suppress NLRP3 inflammasome components in rheumatoid arthritis.

Wen-Xuan Li, Ping Qian, Yi-Tong Guo, Li Gu, Jessore Jurat, Yang Bai, Dong-Fang Zhang

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC complementary medicine and therapies, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

20 citing papers in PubMed, 25 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Wen-Xuan Li *Department of Pharmacognosy, School of Pharmacy, China Medical University, Shenyang, 110122, Liaoning, China.
Ping Qian *Department of Pharmacognosy, School of Pharmacy, China Medical University, Shenyang, 110122, Liaoning, China.
Yi-Tong GuoDepartment of Pharmacognosy, School of Pharmacy, China Medical University, Shenyang, 110122, Liaoning, China.
Li GuDepartment of Pharmacognosy, School of Pharmacy, China Medical University, Shenyang, 110122, Liaoning, China.
Jessore JuratDepartment of Pharmacognosy, School of Pharmacy, China Medical University, Shenyang, 110122, Liaoning, China.
Yang BaiDepartment of Clinical Pharmacology, School of Pharmacy, China Medical University, Shenyang, 110122, Liaoning, China. ybai@cmu.edu.cn.
Dong-Fang ZhangDepartment of Pharmacognosy, School of Pharmacy, China Medical University, Shenyang, 110122, Liaoning, China. dfzhang@cmu.edu.cn.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLiquidambaris Fructus (LF) is the infructescence of Liquidambar formosana. In Traditional Chinese Medicine, LF has been used to treat joint pain, a common symptom of arthritis and rheumatism; however, a lack of pharmacological evidence has limited its applications in modern clinics. Therefore, this study aims to explore the protective effect of LF on rheumatoid arthritis (RA) and to identify its active ingredients.

methodsRats with adjuvant-induced arthritis (AIA) were divided into 4 groups and administered petroleum ether extract of LF (PEL), ethyl acetate extract of LF (EEL), water extract of LF (WEL), or piroxicam (PIR) respectively for 3 weeks. Two additional groups were used as normal control (NC) and model control (MC) and administered distilled water as a placebo. The clinical scores for arthritis, bone surface, synovial inflammation and cartilage erosion were used to evaluate the therapeutic efficacy of each treatment. The serum IL-1β and TNF-α level and the expression of NLRP3, IL-1β and caspase-1 p20 in the synovial tissue of AIA rats were evaluated by ELISA and Western blot. The active ingredients of LF were investigated using network pharmacology and molecular docking methods, and their inhibition of NLRP3 inflammasome activation was verified in the human rheumatoid arthritis fibroblast-like synovial cells (RA-FLS) model.

resultsPEL could alleviate paw swelling, bone and joint destruction, synovial inflammation and cartilage erosion in the AIA rats, with significantly superior efficacy to that of EEL and WEL. PEL reduced IL-1β and TNF-α serum levels, and attenuated the upregulation of NLRP3, IL-1β and caspase-1 p20 expression in the synovial tissue of AIA rats. Network pharmacology and molecular docking results indicated that myrtenal and β-caryophyllene oxide were the main two active ingredients of PEL, and these two compounds showed significant inhibition on TNF-α, NLRP3, IL-1β and caspase-1 p20 expression in RA-FLS.

conclusionsMyrtenal and β-caryophyllene oxide screened from PEL could suppress the activation of NLRP3 inflammasome, thereby alleviating RA symptoms.

Indexed as

AnimalsArthritis, RheumatoidBicyclic MonoterpenesInflammasomesMaleMolecular Docking SimulationNetwork PharmacologyNLR Family, Pyrin Domain-Containing 3 ProteinPolycyclic SesquiterpenesRatsRats, Inbred WFBicyclic Monoterpenescaryophyllene oxideInflammasomesmyrtenalNLR Family, Pyrin Domain-Containing 3 ProteinPolycyclic SesquiterpenesLiquidambaris FructusMyrtenalNLRP3 inflammasomeRheumatoid arthritisβ-Caryophyllene oxide

Identifiers

PMID34583676
PMCPMC8480017
OpenAlexW3204410023

What OpenQuestion holds

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LicenceCC BY
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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.