A Simplified Model of Adenine-Induced Chronic Kidney Disease Using SKH1 Mice

Commonly used adenine-induced chronic kidney disease (CKD) murine models often employ C57BL/6 mice; however, this strain has inherent limitations due to its natural resistance to developing key pathological features of CKD, such as tubulointerstitial fibrosis and inflammation. There have been attempts to overcome these barriers by using multiple concentrations of adenine-supplemented diets or by performing prolonged experiments up to 20 weeks. Here, we demonstrate that SKH1 Elite mice develop clinically relevant CKD phenotypes (e.g., polyuria, proteinuria, inflammation, and renal fibrosis) over the course of only 6 weeks of low-dose (0.15%) adenine supplementation. As a docile, immunocompetent, and hairless strain, SKH1 Elite mice offer several logistical advantages over C57BL/6 mice, including ease of handling and the ability to study dermal conditions, which are often secondary to CKD.

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Publication Details

Journal
Cells
Published
2024-12-20
DOI
https://doi.org/10.3390/cells13242117
Citations
4
Primary Topic
Genetic Syndromes and Imprinting
Type
article
Field-Weighted Citation Impact
2.20

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article

A Simplified Model of Adenine-Induced Chronic Kidney Disease Using SKH1 Mice

Apurva Lad, Benjamin W. French, Steven T. Haller, David J. Kennedy et al.
4 citations
Cells
Genetic Syndromes and Imprinting
2.20
article

A Simplified Model of Adenine-Induced Chronic Kidney Disease Using SKH1 Mice

Apurva Lad, Benjamin W. French, Steven T. Haller, David J. Kennedy, Bivek Timalsina, Amira F. Gohara, Joshua D. Breidenbach, Upasana Shrestha, Prabhatchandra Dube, Bella Khatib-Shahidi, Sara Kazmi, Dhilhani Faleel, D.V. Malhotra, Shereen Yassine, Humza Bashir, Caitlin Murphy, Irum Syed, Satkeerth Boyapalli, Evan M. Benson
article en
4 citations

Abstract

Commonly used adenine-induced chronic kidney disease (CKD) murine models often employ C57BL/6 mice; however, this strain has inherent limitations due to its natural resistance to developing key pathological features of CKD, such as tubulointerstitial fibrosis and inflammation. There have been attempts to overcome these barriers by using multiple concentrations of adenine-supplemented diets or by performing prolonged experiments up to 20 weeks. Here, we demonstrate that SKH1 Elite mice develop clinically relevant CKD phenotypes (e.g., polyuria, proteinuria, inflammation, and renal fibrosis) over the course of only 6 weeks of low-dose (0.15%) adenine supplementation. As a docile, immunocompetent, and hairless strain, SKH1 Elite mice offer several logistical advantages over C57BL/6 mice, including ease of handling and the ability to study dermal conditions, which are often secondary to CKD.

CellsVol. 13(24)
University of Toledo Medical Center (US), Los Alamos National Laboratory (US), University of Toledo (US)
National Science Foundation, University of Toledo, Ohio Department of Higher Education, National Institutes of Health, National Heart, Lung, and Blood Institute
Good health and well-being
Openalex Percentile: Top 11%
Genetic Syndromes and Imprinting
2.20
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