Evidence map›Paper›PMID 31781348›Full record

ArticleOxidative medicine and cellular longevity2019

The 5-Lipoxygenase Inhibitor Zileuton Protects Pressure Overload-Induced Cardiac Remodeling via Activating PPAR

Qing-Qing Wu, Wei Deng, Yang Xiao, Jiao-Jiao Chen, Chen Liu, Juan Wang, Yankai Guo, Mingxia Duan, Zhulan Cai, Saiyang Xie and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-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

18 citing papers in PubMed, 28 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

12 authors at 2 institutions in 1 country.

Qing-Qing WuDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.ORCID https://orcid.org/0000-0002-7475-5014
Wei DengDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.ORCID https://orcid.org/0000-0003-4883-4226
Yang XiaoDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Jiao-Jiao ChenDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Chen LiuDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Juan WangDepartment of Cardiology, The Fifth Affiliated Hospital of Xinjiang Medical University, Ürümqi, China.
Yankai GuoDepartment of Pacing and Electrophysiological, First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang 830011, China.
Mingxia DuanDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Zhulan CaiDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Saiyang XieDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Yuan YuanDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Qizhu TangDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.ORCID https://orcid.org/0000-0003-2210-3169
Wuhan University · CNXinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zileuton has been demonstrated to be an anti-inflammatory agent due to its well-known ability to inhibit 5-lipoxygenase (5-LOX). However, the effects of zileuton on cardiac remodeling are unclear. In this study, the effects of zileuton on pressure overload-induced cardiac remodeling were investigated and the possible mechanisms were examined. Aortic banding was performed on mice to induce a cardiac remodeling model, and the mice were then treated with zileuton 1 week after surgery. We also stimulated neonatal rat cardiomyocytes with phenylephrine (PE) and then treated them with zileuton. Our data indicated that zileuton protected mice from pressure overload-induced cardiac hypertrophy, fibrosis, and oxidative stress. Zileuton also attenuated PE-induced cardiomyocyte hypertrophy in a time- and dose-dependent manner. Mechanistically, we found that zileuton activated PPAR

Indexed as

AnimalsBlood PressureDisease Models, AnimalDose-Response Relationship, DrugHydroxyureaLipoxygenase InhibitorsMaleMiceMyocytes, CardiacNF-E2-Related Factor 2PPAR alphaRatsSignal TransductionVentricular RemodelingHydroxyureaLipoxygenase InhibitorsNfe2l2 protein, mouseNfe2l2 protein, ratNF-E2-Related Factor 2PPAR alphazileuton

Identifiers

PMID31781348
PMCPMC6874937
OpenAlexW2988438318

What OpenQuestion holds

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LicenceCC BY
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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.