Evidence map›Paper›PMID 31475609›Full record

ArticleCell cycle (Georgetown, Tex.)2019

Ethyl pyruvate inhibits LPS induced IPEC-J2 inflammation and apoptosis through p38 and ERK1/2 pathways.

Na Dong, Xinyao Xu, Chenyu Xue, Chensi Wang, Xinran Li, Chongpeng Bi, Anshan Shan

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  7. Ethyl pyruvate, a versatile protector in inflammation and autoimmunity.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    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

7 authors at 1 institution in 1 country.

Na DongFrom the Laboratory of Molecular Nutrition and Immunity, Institute of Animal Nutrition, Northeast Agricultural University , Harbin , P. R. China.
Xinyao XuFrom the Laboratory of Molecular Nutrition and Immunity, Institute of Animal Nutrition, Northeast Agricultural University , Harbin , P. R. China.
Chenyu XueFrom the Laboratory of Molecular Nutrition and Immunity, Institute of Animal Nutrition, Northeast Agricultural University , Harbin , P. R. China.
Chensi WangFrom the Laboratory of Molecular Nutrition and Immunity, Institute of Animal Nutrition, Northeast Agricultural University , Harbin , P. R. China.
Xinran LiFrom the Laboratory of Molecular Nutrition and Immunity, Institute of Animal Nutrition, Northeast Agricultural University , Harbin , P. R. China.
Chongpeng BiFrom the Laboratory of Molecular Nutrition and Immunity, Institute of Animal Nutrition, Northeast Agricultural University , Harbin , P. R. China.
Anshan ShanFrom the Laboratory of Molecular Nutrition and Immunity, Institute of Animal Nutrition, Northeast Agricultural University , Harbin , P. R. China.
Northeast Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endotoxin of Gram-negative bacteria threatens the intestinal health of livestock. Ethyl pyruvate (EP) has been shown to regulate intestinal immunity and protect against cell and tissue damage. In this study, it was first verified that EP could reduce the secretion of IL-8, TNF-α, IL-6 and IL-1β in LPS-induced IPEC-J2 cells. Then, we used RNA sequencing (RNA-seq) to analyze the differentially expressed genes (DEGs) of inflammatory factors induced by LPS in IPEC-J2 cells. It was found that LPS induced the upregulation of 377 genes and the downregulation of 477 genes compared to Vehicle; LPS+EP induced the upregulation of 258 genes and the downregulation of 240 genes compared to Vehicle; and LPS+EP induced the upregulation of 373 genes and the downregulation of 188 genes compared to LPS (fold change > 1.5 and FDR < 0.01). Their enrichment pathways included the MAPK signaling pathway, PI3K-Akt signaling pathway, Toll-like receptor signaling pathway, and other pathways. Furthermore, the mRNA level of cytokines associated with inflammation and apoptosis enriched in the MAPK pathway was verified by qRT-PCR. Western blots and immunofluorescence revealed that EP significantly inhibited phosphorylated p38 and phosphorylated-ERK1/2 protein expression levels (

Indexed as

AnimalsApoptosisCell LineCytokinesDown-RegulationEnterocytesInflammationLipopolysaccharidesMAP Kinase Signaling Systemp38 Mitogen-Activated Protein KinasesPyruvatesRNA, MessengerRNA-SeqSignal TransductionSwineUp-RegulationCytokinesethyl pyruvateLipopolysaccharidesp38 Mitogen-Activated Protein KinasesPyruvatesRNA, MessengerApoptosisEthyl pyruvateMAPKPorcine jejunal epithelial cellsRNA-seq

Identifiers

PMID31475609
PMCPMC6773235
OpenAlexW2971471076

What OpenQuestion holds

Textmetadata
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.