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Uraemic Cardiomyopathy in Different Mouse Models

Uraemic cardiomyopathy (UCM) is one of the most common complications in chronic kidney disease (CKD). Our aim was to compare characteristics of various UCM mouse models. Mice were assigned to the following groups: the pole ligation group, 5/6 nephrectomy group (5/6Nx), uninephrectomy plus contralate...

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Autores principales: Chen, Cheng, Xie, Caidie, Wu, Hanzhang, Wu, Lin, Zhu, Jingfeng, Mao, Huijuan, Xing, Changying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316724/
https://www.ncbi.nlm.nih.gov/pubmed/34336893
http://dx.doi.org/10.3389/fmed.2021.690517
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author Chen, Cheng
Xie, Caidie
Wu, Hanzhang
Wu, Lin
Zhu, Jingfeng
Mao, Huijuan
Xing, Changying
author_facet Chen, Cheng
Xie, Caidie
Wu, Hanzhang
Wu, Lin
Zhu, Jingfeng
Mao, Huijuan
Xing, Changying
author_sort Chen, Cheng
collection PubMed
description Uraemic cardiomyopathy (UCM) is one of the most common complications in chronic kidney disease (CKD). Our aim was to compare characteristics of various UCM mouse models. Mice were assigned to the following groups: the pole ligation group, 5/6 nephrectomy group (5/6Nx), uninephrectomy plus contralateral ischemia followed by reperfusion group (IR), adenine group, and sham group. Mice were sacrificed at 4, 8, and 16 weeks after surgery in the pole ligation, 5/6Nx, and IR groups, respectively. In the adenine group, mice were sacrificed at 16 weeks after the adenine diet. The structure and function of the heart and the expression of fibroblast growth factor 23 (FGF-23) and growth differentiation factor 15 (GDF-15) in hearts were assessed. The mortality in the 5/6 Nx group was significantly higher than that in the pole ligation, IR, and adenine groups. Echocardiogram and histological examination showed cardiac hypertrophy in the adenine,5/6Nx, ligation group, and IR group. In addition, cardiac fibrosis occurred in all CKD modeling groups. Interestingly, cardiac fibrosis was more serious in the IR and adenine groups. FGF-23 expression in sham mice was similar to that in modeling groups; however, the GDF-15 level was decreased in modeling groups. Our results suggest that the four models of UCM show different phenotypical features, molding time and mortality. GDF-15 expression in the hearts of UCM mice was downregulated compared with sham group mice.
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spelling pubmed-83167242021-07-29 Uraemic Cardiomyopathy in Different Mouse Models Chen, Cheng Xie, Caidie Wu, Hanzhang Wu, Lin Zhu, Jingfeng Mao, Huijuan Xing, Changying Front Med (Lausanne) Medicine Uraemic cardiomyopathy (UCM) is one of the most common complications in chronic kidney disease (CKD). Our aim was to compare characteristics of various UCM mouse models. Mice were assigned to the following groups: the pole ligation group, 5/6 nephrectomy group (5/6Nx), uninephrectomy plus contralateral ischemia followed by reperfusion group (IR), adenine group, and sham group. Mice were sacrificed at 4, 8, and 16 weeks after surgery in the pole ligation, 5/6Nx, and IR groups, respectively. In the adenine group, mice were sacrificed at 16 weeks after the adenine diet. The structure and function of the heart and the expression of fibroblast growth factor 23 (FGF-23) and growth differentiation factor 15 (GDF-15) in hearts were assessed. The mortality in the 5/6 Nx group was significantly higher than that in the pole ligation, IR, and adenine groups. Echocardiogram and histological examination showed cardiac hypertrophy in the adenine,5/6Nx, ligation group, and IR group. In addition, cardiac fibrosis occurred in all CKD modeling groups. Interestingly, cardiac fibrosis was more serious in the IR and adenine groups. FGF-23 expression in sham mice was similar to that in modeling groups; however, the GDF-15 level was decreased in modeling groups. Our results suggest that the four models of UCM show different phenotypical features, molding time and mortality. GDF-15 expression in the hearts of UCM mice was downregulated compared with sham group mice. Frontiers Media S.A. 2021-07-14 /pmc/articles/PMC8316724/ /pubmed/34336893 http://dx.doi.org/10.3389/fmed.2021.690517 Text en Copyright © 2021 Chen, Xie, Wu, Wu, Zhu, Mao and Xing. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Chen, Cheng
Xie, Caidie
Wu, Hanzhang
Wu, Lin
Zhu, Jingfeng
Mao, Huijuan
Xing, Changying
Uraemic Cardiomyopathy in Different Mouse Models
title Uraemic Cardiomyopathy in Different Mouse Models
title_full Uraemic Cardiomyopathy in Different Mouse Models
title_fullStr Uraemic Cardiomyopathy in Different Mouse Models
title_full_unstemmed Uraemic Cardiomyopathy in Different Mouse Models
title_short Uraemic Cardiomyopathy in Different Mouse Models
title_sort uraemic cardiomyopathy in different mouse models
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316724/
https://www.ncbi.nlm.nih.gov/pubmed/34336893
http://dx.doi.org/10.3389/fmed.2021.690517
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