Evidence map›Paper›PMID 36555694›Full record

ArticleInternational journal of molecular sciences2022

β-Caryophyllene Acts as a Ferroptosis Inhibitor to Ameliorate Experimental Colitis.

Yan-Ting Wu, Li-Shan Zhong, Chen Huang, Yu-Ying Guo, Fu-Jun Jin, Yu-Ze Hu, Zi-Bo Zhao, Zhe Ren, Yi-Fei Wang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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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

9 authors at 1 institution in 1 country.

Yan-Ting WuDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.ORCID 0000-0003-1386-3422
Li-Shan ZhongDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Chen HuangDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Yu-Ying GuoDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Fu-Jun JinDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Yu-Ze HuDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Zi-Bo ZhaoDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Zhe RenDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.ORCID 0000-0001-7573-5288
Yi-Fei WangDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.ORCID 0000-0002-9918-2865
Jinan University · CN

Funding

Department of Agriculture of Guangdong Province 2020KJ142Department of Agriculture of Guangdong Province 2021KJ142Science and Technology Bureau of Guangzhou Municipality 202206010008
6 · The paper itself

Abstract

Macrophage infiltration is one of the main pathological features of ulcerative colitis (UC) and ferroptosis is a type of nonapoptotic cell death, connecting oxidative stress and inflammation. However, whether ferroptosis occurs in the colon macrophages of UC mice and whether targeting macrophage ferroptosis is an effective approach for UC treatment remain unclear. The present study revealed that macrophage lipid peroxidation was observed in the colon of UC mice. Subsequently, we screened several main components of essential oil from Artemisia argyi and found that β-caryophyllene (BCP) had a good inhibitory effect on macrophage lipid peroxidation. Additionally, ferroptotic macrophages were found to increase the mRNA expression of tumor necrosis factor alpha (Tnf-α) and prostaglandin-endoperoxide synthase 2 (Ptgs2), while BCP can reverse the effects of inflammation activated by ferroptosis. Further molecular mechanism studies revealed that BCP activated the type 2 cannabinoid receptor (CB2R) to inhibit macrophage ferroptosis and its induced inflammatory response both in vivo and in vitro. Taken together, BCP potentially ameliorated experimental colitis inflammation by inhibiting macrophage ferroptosis. These results revealed that macrophage ferroptosis is a potential therapeutic target for UC and identified a novel mechanism of BCP in ameliorating experimental colitis.

Indexed as

ColitisColitis, UlcerativeFerroptosisAnimalsDextran SulfateInflammationMicePolycyclic SesquiterpenescaryophylleneDextran SulfatePolycyclic Sesquiterpenesferroptosisinflammationmacrophagetype 2 cannabinoid receptorulcerative colitisβ-caryophyllene

Identifiers

PMID36555694
PMCPMC9784863
OpenAlexW4312211215

What OpenQuestion holds

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LicenceCC BY
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.