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Oxalate-induced chronic kidney disease with its uremic and cardiovascular complications in C57BL/6 mice.
Mulay, Shrikant R; Eberhard, Jonathan N; Pfann, Victoria; Marschner, Julian A; Darisipudi, Murthy N; Daniel, Christoph; Romoli, Simone; Desai, Jyaysi; Grigorescu, Melissa; Kumar, Santhosh V; Rathkolb, Birgit; Wolf, Eckhard; Hrabe de Angelis, Martin; Bäuerle, Tobias; Dietel, Barbara; Wagner, Carsten A; Amann, Kerstin; Eckardt, Kai-Uwe; Aronson, Peter S; Anders, Hans Joachim; Knauf, Felix.
Afiliação
  • Mulay SR; Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany.
  • Eberhard JN; Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany.
  • Pfann V; Department of Nephrology and Hypertension, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
  • Marschner JA; Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany.
  • Darisipudi MN; Department of Nephrology and Hypertension, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
  • Daniel C; Department of Nephropathology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
  • Romoli S; Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany.
  • Desai J; Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany.
  • Grigorescu M; Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany.
  • Kumar SV; Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany.
  • Rathkolb B; German Mouse Clinic, Institute of Experimental Genetics, Helmholtz-Zentrum München, Neuherberg, Germany.
  • Wolf E; Institute of Molecular Animal Breeding and Biotechnology, Gene Center, Ludwig-Maximilians-University München, Munich, Germany.
  • Hrabe de Angelis M; Institute of Molecular Animal Breeding and Biotechnology, Gene Center, Ludwig-Maximilians-University München, Munich, Germany.
  • Bäuerle T; German Mouse Clinic, Institute of Experimental Genetics, Helmholtz-Zentrum München, Neuherberg, Germany.
  • Dietel B; School of Life Science Weihenstephan, Technische Universität München, Freising, Germany.
  • Wagner CA; German Center for Diabetes Research (DZD), Neuherberg, Germany.
  • Amann K; Preclinical Imaging Platform Erlangen, Institute of Radiology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
  • Eckardt KU; Department of Cardiology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
  • Aronson PS; Zurich Center for Integrative Human Physiology, Zurich, Switzerland; and.
  • Anders HJ; Department of Nephropathology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
  • Knauf F; Department of Nephrology and Hypertension, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
Am J Physiol Renal Physiol ; 310(8): F785-F795, 2016 04 15.
Article em En | MEDLINE | ID: mdl-26764204
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Uremia / Ácido Oxálico / Modelos Animais de Doenças / Insuficiência Renal Crônica / Hipertensão Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Uremia / Ácido Oxálico / Modelos Animais de Doenças / Insuficiência Renal Crônica / Hipertensão Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article