Evidence map›Paper›PMID 35541316›Full record

ArticleRSC advances2018

Pharmacological inhibition of fatty acid-binding protein 4 (FABP4) protects against renal ischemia-reperfusion injury.

Min Shi, Rongshuang Huang, Fan Guo, Lingzhi Li, Yanhuan Feng, Zhengjie Wei, Li Zhou, Liang Ma, Ping Fu

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2018. 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
1.1field-weighted citation impact, top 23% 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, 24 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

9 authors at 2 institutions in 2 countries.

Min ShiKidney Research Institute, Division of Nephrology, West China Hospital of Sichuan University Chengdu 610041 No. 37 Guoxue Allay China Liang_m@scu.edu.cn fupinghx@163.com +86-28-85423341 +86-28-85164167.
Rongshuang HuangKidney Research Institute, Division of Nephrology, West China Hospital of Sichuan University Chengdu 610041 No. 37 Guoxue Allay China Liang_m@scu.edu.cn fupinghx@163.com +86-28-85423341 +86-28-85164167.
Fan GuoKidney Research Institute, Division of Nephrology, West China Hospital of Sichuan University Chengdu 610041 No. 37 Guoxue Allay China Liang_m@scu.edu.cn fupinghx@163.com +86-28-85423341 +86-28-85164167.
Lingzhi LiKidney Research Institute, Division of Nephrology, West China Hospital of Sichuan University Chengdu 610041 No. 37 Guoxue Allay China Liang_m@scu.edu.cn fupinghx@163.com +86-28-85423341 +86-28-85164167.
Yanhuan FengKidney Research Institute, Division of Nephrology, West China Hospital of Sichuan University Chengdu 610041 No. 37 Guoxue Allay China Liang_m@scu.edu.cn fupinghx@163.com +86-28-85423341 +86-28-85164167.
Zhengjie WeiChengdu No. 7 High School Chengdu 610041 China.
Li ZhouKidney Research Institute, Division of Nephrology, West China Hospital of Sichuan University Chengdu 610041 No. 37 Guoxue Allay China Liang_m@scu.edu.cn fupinghx@163.com +86-28-85423341 +86-28-85164167.
Liang MaKidney Research Institute, Division of Nephrology, West China Hospital of Sichuan University Chengdu 610041 No. 37 Guoxue Allay China Liang_m@scu.edu.cn fupinghx@163.com +86-28-85423341 +86-28-85164167.ORCID https://orcid.org/0000-0001-8327-7969
Ping FuKidney Research Institute, Division of Nephrology, West China Hospital of Sichuan University Chengdu 610041 No. 37 Guoxue Allay China Liang_m@scu.edu.cn fupinghx@163.com +86-28-85423341 +86-28-85164167.
Sichuan University · CNChengdu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fatty acid-binding protein 4 (FABP4) is a key mediator of endoplasmic reticulum (ER) stress and apoptosis in diabetes and atherosclerosis. Studies also confirmed that circulating FABP4 depended on renal function in chronic kidney disease (CKD) and acute kidney injury (AKI) patients. However, the function of FABP4 in AKI remains poorly understood and the aim of this study was to investigate the role of FABP4 in ischemia-reperfusion (I/R)-induced AKI. In the present study, renal I/R injury triggered the high expression of the FABP4 gene and protein in the nucleus and cytoplasm of tubular cells of mouse kidney tissue compared to that of Sham. Pretreatment with BMS309403, a highly selective inhibitor of FABP4 at a dose of 20 mg kg

Identifiers

PMID35541316
PMCPMC9079974
OpenAlexW2801448258

What OpenQuestion holds

Textmetadata
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.