Oxalate-induced chronic kidney disease with its uremic and cardiovascular complications in C57BL/6 mice

Author:

Mulay Shrikant R.1,Eberhard Jonathan N.1,Pfann Victoria2,Marschner Julian A.1,Darisipudi Murthy N.2,Daniel Christoph3,Romoli Simone1,Desai Jyaysi1,Grigorescu Melissa1,Kumar Santhosh V.1,Rathkolb Birgit45,Wolf Eckhard5,Hrabě de Angelis Martin467,Bäuerle Tobias8,Dietel Barbara9,Wagner Carsten A.10ORCID,Amann Kerstin3,Eckardt Kai-Uwe2,Aronson Peter S.1,Anders Hans Joachim1,Knauf Felix211

Affiliation:

1. Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany;

2. Department of Nephrology and Hypertension, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany;

3. Department of Nephropathology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany;

4. German Mouse Clinic, Institute of Experimental Genetics, Helmholtz-Zentrum München, Neuherberg, Germany;

5. Institute of Molecular Animal Breeding and Biotechnology, Gene Center, Ludwig-Maximilians-University München, Munich, Germany;

6. School of Life Science Weihenstephan, Technische Universität München, Freising, Germany;

7. German Center for Diabetes Research (DZD), Neuherberg, Germany;

8. Preclinical Imaging Platform Erlangen, Institute of Radiology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany;

9. Department of Cardiology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany;

10. Zurich Center for Integrative Human Physiology, Zurich, Switzerland; and

11. Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut

Abstract

Chronic kidney disease (CKD) research is limited by the lack of convenient inducible models mimicking human CKD and its complications in experimental animals. We demonstrate that a soluble oxalate-rich diet induces stable stages of CKD in male and female C57BL/6 mice. Renal histology is characterized by tubular damage, remnant atubular glomeruli, interstitial inflammation, and fibrosis, with the extent of tissue involvement depending on the duration of oxalate feeding. Expression profiling of markers and magnetic resonance imaging findings established to reflect inflammation and fibrosis parallel the histological changes. Within 3 wk, the mice reproducibly develop normochromic anemia, metabolic acidosis, hyperkalemia, FGF23 activation, hyperphosphatemia, and hyperparathyroidism. In addition, the model is characterized by profound arterial hypertension as well as cardiac fibrosis that persist following the switch to a control diet. Together, this new model of inducible CKD overcomes a number of previous experimental limitations and should serve useful in research related to CKD and its complications.

Publisher

American Physiological Society

Subject

Physiology

Cited by 71 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3