Evidence map›Paper›PMID 35562673›Full record

ArticleBMC nephrology2022

Statins attenuate cholesterol-induced ROS via inhibiting NOX2/NOX4 and mitochondrial pathway in collecting ducts of the kidney.

Ani Wang, Yu Lin, Baien Liang, Xiaoduo Zhao, Miaojuan Qiu, Hui Huang, Chunling Li, Weidong Wang, Yonglun Kong

Open access · goldAbstract read
In one paragraph

Article in BMC nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 15 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 1 country.

Ani WangCardiovascular Center, The 5thAffiliated Hospital, Sun Yat-Sen University, Zhuhai, 519000, China.
Yu LinDepartment of Pathology, Zhujiang Hospitial, Southern Medical University, Guangzhou, 510282, China.
Baien LiangDepartment of Pathophysiology, Zhongshan School of Medicine, Sun Yat-Sen University, 74# Zhongshan 2nd Road, Guangzhou, 510080, China.
Xiaoduo ZhaoDepartment of Pathophysiology, Zhongshan School of Medicine, Sun Yat-Sen University, 74# Zhongshan 2nd Road, Guangzhou, 510080, China.
Miaojuan QiuResearch Center, The 7th Affiliated Hospital, Sun Yat-Sen University, Shenzhen, 518107, China.
Hui HuangDepartment of Cardiology, The 8th Affiliated Hospital, Sun Yat-Sen University, Shenzhen, 518033, China.
Chunling LiInstitute of Hypertension, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, 510080, China.
Weidong WangDepartment of Pathophysiology, Zhongshan School of Medicine, Sun Yat-Sen University, 74# Zhongshan 2nd Road, Guangzhou, 510080, China. wangwd6@mail.sysu.edu.cn.
Yonglun KongDepartment of Pathophysiology, Zhongshan School of Medicine, Sun Yat-Sen University, 74# Zhongshan 2nd Road, Guangzhou, 510080, China. winlingkong@163.com.
Sun Yat-sen University · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStatins therapy has been primarily recommended for the prevention of cardiovascular risk in patients with chronic kidney diseases. Statins has also been proved some benefits in lipid-induced kidney diseases. The current study aims to investigate the protection and underlying mechanisms of statins on renal tubular injuries induced by cholesterol overloaded.

methodsWe used tubular suspensions of inner medullary collecting duct (IMCD) cells from rat kidneys and mouse collecting duct cell line mpkCCD cells to investigate the effect of statins on reactive oxygen species (ROS) production induced by cholesterol. Protein and mRNA expression of NADPH oxidase 2 (NOX2) /NOX4 was examined by Western blot and RT-PCR in vitro studies and in rats with 5/6 nephrectomy and high-fat diet. Mitochondrial morphology and membrane potential was observed by Mito-tracker and JC-1.

resultsStatins treatment was associated with decreased NOX2 and NOX4 protein expression and mRNA levels in 5/6Nx rats with high-fat diet. Statins treatment markedly reduced the ROS production in IMCD suspensions and mpkCCD cells. Also, statins reduced NOX2 and NOX4 protein expression and mRNA levels in cholesterol overload mpkCCD cells and improved mitochondrial morphology and function.

conclusionStatins prevented ROS production induced by cholesterol in the kidney, likely through inhibiting NOXs protein expression and improving mitochondrial function. Statins may be a therapeutic option in treating obesity-associated kidney diseases.

Indexed as

Hydroxymethylglutaryl-CoA Reductase InhibitorsRenal Insufficiency, ChronicAnimalsCholesterolKidneyMaleMiceMitochondriaNADPH Oxidase 2NADPH Oxidase 4RatsReactive Oxygen SpeciesRNA, MessengerCholesterolCybb protein, mouseCybb protein, ratHydroxymethylglutaryl-CoA Reductase InhibitorsNADPH Oxidase 2NADPH Oxidase 4Nox4 protein, mouseNox4 protein, ratReactive Oxygen SpeciesRNA, MessengerCholesterolCollecting ductsROSStatins

Identifiers

PMID35562673
PMCPMC9102638
OpenAlexW4280489041

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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.