Evidence map›Paper›PMID 38472560›Full record

ArticleCellular and molecular life sciences : CMLS2024

PEBP4 deficiency aggravates LPS-induced acute lung injury and alveolar fluid clearance impairment via modulating PI3K/AKT signaling pathway.

Qiao-Qing Shi, Yong-Hong Huang, Yu-Fei Li, Shuang-Yan Zhen, Yan-Hong Li, Jia-Yi Huang, Jia-Yang Wang, Xiao-Yan Zhou

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

8 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

8 authors at 2 institutions in 1 country.

Qiao-Qing Shi *Department of Pathophysiology, School of Basic Medical Sciences, Jiangxi Medical College, Nanchang University, 461 BaYi Road, Nanchang, 330006, Jiangxi, P.R. China.
Yong-Hong Huang *Department of Pathophysiology, School of Basic Medical Sciences, Jiangxi Medical College, Nanchang University, 461 BaYi Road, Nanchang, 330006, Jiangxi, P.R. China.
Yu-Fei LiDepartment of Pathophysiology, School of Basic Medical Sciences, Jiangxi Medical College, Nanchang University, 461 BaYi Road, Nanchang, 330006, Jiangxi, P.R. China.
Shuang-Yan ZhenSino-German Joint Research Institute, Nanchang University, Nanchang, 330047, China.
Yan-Hong LiDepartment of Forensic Medicine, School of Basic Medical Sciences, Jiangxi Medical College, Nanchang University, Nanchang, 330006, China.
Jia-Yi HuangSchool of Basic Medical Sciences, Nanchang University, Nanchang, 330103, China.
Jia-Yang WangSchool of Stomatology, Nanchang University, Nanchang, 330103, China.
Xiao-Yan ZhouDepartment of Pathophysiology, School of Basic Medical Sciences, Jiangxi Medical College, Nanchang University, 461 BaYi Road, Nanchang, 330006, Jiangxi, P.R. China. zhouxiaoyan@ncu.edu.cn.ORCID http://orcid.org/0000-0002-0509-2974
Nanchang University · CNFirst Affiliated Hospital of Jiangxi Medical College · CN

Funding

innovation and entrepreneurship training program of Nanchang University 2023CX007Jiangxi innovation and entrepreneurship training program S202310403070Nanchang University ZBG20230418040National Natural Science Foundation of China 81660163National Natural Science Foundation of China 82360125 and 81760117
6 · The paper itself

Abstract

Acute lung injury (ALI) is a common clinical syndrome, which often results in pulmonary edema and respiratory distress. It has been recently reported that phosphatidylethanolamine binding protein 4 (PEBP4), a basic cytoplasmic protein, has anti-inflammatory and hepatoprotective effects, but its relationship with ALI remains undefined so far. In this study, we generated PEBP4 knockout (KO) mice to investigate the potential function of PEBP4, as well as to evaluate the capacity of alveolar fluid clearance (AFC) and the activity of phosphatidylinositide 3-kinases (PI3K)/serine-theronine protein kinase B (PKB, also known as AKT) signaling pathway in lipopolysaccharide (LPS)-induced ALI mice models. We found that PEBP4 deficiency exacerbated lung pathological damage and edema, and increased the wet/dry weight ratio and total protein concentration of bronchoalveolar lavage fluid (BALF) in LPS-treated mice. Meanwhile, PEBP4 KO promoted an LPS-induced rise in the pulmonary myeloperoxidase (MPO) activity, serum interleuin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α levels, and pulmonary cyclooxygenase-2 (COX-2) expression. Mechanically, PEBP4 deletion further reduced the protein expression of Na

Indexed as

Acute Lung InjuryLipopolysaccharidesAnimalsLungMicePhosphatidylethanolamine Binding ProteinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionSodium-Potassium-Exchanging ATPaseTumor Necrosis Factor-alphaLipopolysaccharidesPEBP4 protein, mousePhosphatidylethanolamine Binding ProteinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSodium-Potassium-Exchanging ATPaseTumor Necrosis Factor-alphaAcute lung injuryAlveolar fluid clearanceInflammatory responsePhosphatidylethanolamine binding protein 4 (PEBP4)PI3K/AKT signaling pathway

Identifiers

PMID38472560
PMCPMC10933182
OpenAlexW4392742267

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.