Evidence map›Paper›PMID 36987783›Full record

ArticleBrain and behavior2023

JNK-IN-8 treatment improves ARDS-induced cognitive impairment by inhibiting JNK/NF-κB-mediated NLRP3 inflammasome.

Yunchao Shi, Ying Fang, Peng Shen, He Liu, Longsheng Xu, Liyan Wang, Maoxian Yang

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 6 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 2 institutions in 1 country.

Yunchao ShiDepartment of Intensive Care Unit, The First Hospital of Jiaxing & First Affiliated Hospital of Jiaxing University, Jiaxing, China.
Ying FangDepartment of Pathology, The First Hospital of Jiaxing & First Affiliated Hospital of Jiaxing University, Jiaxing, China.
Peng ShenDepartment of Intensive Care Unit, The First Hospital of Jiaxing & First Affiliated Hospital of Jiaxing University, Jiaxing, China.
He LiuDepartment of Anesthesiology, The Affiliated Huzhou Hospital, Zhejiang University School of Medicine & Huzhou Central Hospital, Huzhou, China.
Longsheng XuDepartment of Central Laboratory, The First Hospital of Jiaxing & First Affiliated Hospital of Jiaxing University, Jiaxing, China.
Liyan WangDepartment of General Practice, The First Hospital of Jiaxing & First Affiliated Hospital of Jiaxing University, Jiaxing, China.
Maoxian YangDepartment of Intensive Care Unit, The First Hospital of Jiaxing & First Affiliated Hospital of Jiaxing University, Jiaxing, China.ORCID 0000-0003-0590-6015
Jiaxing University · CNHuzhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCognitive impairment is a critical complication of acute respiratory distress syndrome (ARDS). However, effective interventions are lacking. Growing evidence demonstrates that c-Jun N-terminal kinase (JNK)-mediated neuroinflammation is involved in the development of ARDS. Therefore, we hypothesized that the JNK pathway is involved in ARDS-induced cognitive impairment.

methodsAn in vivo rat model of ARDS was established by treating it with lipopolysaccharide. The cognitive function was assessed by behavioral tests. The levels of pro-inflammatory cytokines, JNK and NOD-, LRR-, and pyrin domain-containing protein 3 (NLRP3) were analyzed by enzyme-linked immunosorbent assay, western blot, or immunohistochemical analysis.

resultsWe found that JNK inhibitor 8 (JNK-IN-8) alleviated cognitive impairment, neuroinflammation, and NLRP3 inflammasome activation in the ARDS rat model. Additionally, an in vivo study showed that the protective effect of JNK-IN-8 on cognitive impairment was blocked by nigericin, an NLRP3 activator.

conclusionsOur data suggest that JNK-IN-8 treatment improves ARDS-induced cognitive impairment by inhibiting the JNK/nuclear factor-κB-mediated NLRP3 inflammasome.

Indexed as

Cognitive DysfunctionInflammasomesAnimalsBenzamidesMAP Kinase Signaling SystemNeuroinflammatory DiseasesNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinPyridinesPyrimidinesRatsBenzamidesInflammasomesJNK-IN-8NF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, ratPyridinesPyrimidinesacute respiratory distress syndromecognitive impairmentJNK-IN-8JNK/NF-κB pathwayNLRP3 inflammasome

Identifiers

PMID36987783
PMCPMC10175986
OpenAlexW4361298684

What OpenQuestion holds

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Registered trials

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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.