Evidence map›Paper›PMID 30011811›Full record

ArticleInternational journal of molecular sciences2018

Farrerol Ameliorates TNBS-Induced Colonic Inflammation by Inhibiting ERK1/2, JNK1/2, and NF-κB Signaling Pathway.

Xin Ran, Yuhang Li, Guangxin Chen, Shoupeng Fu, Dewei He, Bingxu Huang, Libin Wei, Yuanqing Lin, Yingcheng Guo, Guiqiu Hu

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  12. IL-22-ActivatedCells · 2023
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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

10 authors.

Xin RanCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. ranxin9914@mails.jlu.edu.cn.
Yuhang LiCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. yhli9915@mails.jlu.edu.cn.
Guangxin ChenCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. gxchen51143@163.com.
Shoupeng FuCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. fushoupeng@jlu.edu.cn.
Dewei HeCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. m13144303829@163.com.
Bingxu HuangCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. huanbingxu123@163.com.
Libin WeiJiangsu Province Science and Technology Bureau, Taicang 215400, China. shoupengfu@163.com.
Yuanqing LinAnimal Disease Prevention and Control Center of Qinghai Province, Xining 810001, China. lin_yq000@163.com.
Yingcheng GuoJilin Fengman Area Animal Epidemic Prevention and Control Center, Jilin 132013, China. hongqixumu@163.com.
Guiqiu HuCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. guiqiuhu@jlu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Farrerol, a type of 2, 3-dihydro-flavonoid, is obtained from Rhododendron. Previous studies have shown that Farrerol performs multiple biological activities, such as anti-inflammatory, antibacterial, and antioxidant activity. In this study, we aim to investigate the effect of Farrerol on colonic inflammation and explore its potential mechanisms. We found that the effect of Farrerol was evaluated via the 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis model in mice and found that Farrerol has a protective effect on TNBS-induced colitis. Farrerol administration significantly improved the weight change, clinical scores, colon length, and intestinal epithelium barrier damage and markedly decreased the inflammatory cytokines production in TNBS-induced mice. The protective effect of Farrerol was also observed in LPS-induced RAW264.7 cells. We found that Farrerol observably reduced the production of inflammatory mediators including IL-1β, IL-6, TNF-α, COX-2, and iNOS in LPS-induced RAW264.7 cells via suppressing AKT, ERK1/2, JNK1/2, and NF-κB p65 phosphorylation. In conclusion, the study found that Farrerol has a beneficial effect on TNBS-induced colitis and might be a natural therapeutic agent for IBD treatment.

Indexed as

AnimalsChromonesColitisCytokinesLipopolysaccharidesMacrophagesMiceMice, Inbred C57BLMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Mitogen-Activated Protein Kinase 8Mitogen-Activated Protein Kinase 9Mitogen-Activated Protein KinasesNF-kappa BPhytotherapyRAW 264.7 CellsChromonesCytokinesfarrerolLipopolysaccharidesMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Mitogen-Activated Protein Kinase 8Mitogen-Activated Protein Kinase 9Mitogen-Activated Protein KinasesNF-kappa BTrinitrobenzenesulfonic AcidcolitisFarrerolIBDMAPKNF-κB

Identifiers

PMID30011811
PMCPMC6073308

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.