Evidence map›Paper›PMID 29375207›Full record

ArticleWorld journal of gastroenterology2018

β-arrestin 2 attenuates lipopolysaccharide-induced liver injury

Meng-Ping Jiang, Chun Xu, Yun-Wei Guo, Qian-Jiang Luo, Lin Li, Hui-Ling Liu, Jie Jiang, Hui-Xin Chen, Xiu-Qing Wei

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

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  8. GABAPsychopharmacology · 2019
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  9. Ethnopharmacological Inspections of Organic Extract ofEvidence-based complementary and alternative medicine : eCAM · 2019
    Article
  10. 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

9 authors at 3 institutions in 1 country.

Meng-Ping JiangDepartment of Digestive Diseases, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, Guangdong Province, China.
Chun XuDepartment of Digestive Diseases, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, Guangdong Province, China.
Yun-Wei GuoDepartment of Digestive Diseases, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, Guangdong Province, China.
Qian-Jiang LuoDepartment of Digestive Diseases, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, Guangdong Province, China.
Lin LiDepartment of Digestive Diseases, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, Guangdong Province, China.
Hui-Ling LiuDepartment of Digestive Diseases, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, Guangdong Province, China.
Jie JiangDepartment of Digestive Diseases, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, Guangdong Province, China.
Hui-Xin ChenDepartment of Digestive Diseases, Huizhou Municipal Center Hospital, Huizhou 516002, Guangdong Province, China.
Xiu-Qing WeiDepartment of Digestive Diseases, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, Guangdong Province, China. weixq@mail.sysu.edu.cn.
Third Affiliated Hospital of Sun Yat-sen University · CNSun Yat-sen University · CNHuizhou Central People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo study the role and the possible mechanism of β-arrestin 2 in lipopolysaccharide (LPS)-induced liver injury

methodsMale β-arrestin 2

resultsCompared with wild-type mice, the β-arrestin 2 knockout mice displayed more severe LPS-induced liver injury and significantly higher levels of pro-inflammatory cytokines, including interleukin (IL)-1β, IL-6, tumor necrosis factor (TNF)-α, and IL-10. Compared with the control group, pro-inflammatory cytokines (including IL-1β, IL-6, TNF-α, and IL-10) produced by RAW264.7 cells in the β-arrestin 2 siRNA group were significantly increased at 6 h after treatment with LPS. Further, key molecules involved in the TLR4/NF-κB signaling pathway, including phospho-IκBα and phosho-p65, were upregulated.

conclusionβ-arrestin 2 can protect liver tissue from LPS-induced injury

Indexed as

LipopolysaccharidesSignal TransductionAnimalsbeta-Arrestin 2Chemical and Drug Induced Liver InjuryCytokinesDisease Models, AnimalInflammation MediatorsLiverMaleMiceMice, Inbred C57BLMice, KnockoutNF-kappa BNF-KappaB Inhibitor alphaPhosphorylationArrb2 protein, mousebeta-Arrestin 2CytokinesInflammation MediatorsLipopolysaccharidesNF-kappa BNF-KappaB Inhibitor alphaNfkbia protein, mouseRela protein, mouseTlr4 protein, mouseToll-Like Receptor 4Transcription Factor RelALipopolysaccharideLiver injuryPro-inflammatory cytokinesTLR4/NF-κB signaling pathwayβ-arrestin 2

Identifiers

PMID29375207
PMCPMC5768940
OpenAlexW2784283904

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.