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High resolution molecular and histological analysis of renal disease progression in ZSF1 fa/fa(CP) rats, a model of type 2 diabetic nephropathy
ZSF1 rats exhibit spontaneous nephropathy secondary to obesity, hypertension, and diabetes, and have gained interest as a model system with potentially high translational value to progressive human disease. To thoroughly characterize this model, and to better understand how closely it recapitulates...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529026/ https://www.ncbi.nlm.nih.gov/pubmed/28746409 http://dx.doi.org/10.1371/journal.pone.0181861 |
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author | Dower, Ken Zhao, Shanrong Schlerman, Franklin J. Savary, Leigh Campanholle, Gabriela Johnson, Bryce G. Xi, Li Nguyen, Vuong Zhan, Yutian Lech, Matthew P. Wang, Ju Nie, Qing Karsdal, Morten A. Genovese, Federica Boucher, Germaine Brown, Thomas P. Zhang, Baohong Homer, Bruce L. Martinez, Robert V. |
author_facet | Dower, Ken Zhao, Shanrong Schlerman, Franklin J. Savary, Leigh Campanholle, Gabriela Johnson, Bryce G. Xi, Li Nguyen, Vuong Zhan, Yutian Lech, Matthew P. Wang, Ju Nie, Qing Karsdal, Morten A. Genovese, Federica Boucher, Germaine Brown, Thomas P. Zhang, Baohong Homer, Bruce L. Martinez, Robert V. |
author_sort | Dower, Ken |
collection | PubMed |
description | ZSF1 rats exhibit spontaneous nephropathy secondary to obesity, hypertension, and diabetes, and have gained interest as a model system with potentially high translational value to progressive human disease. To thoroughly characterize this model, and to better understand how closely it recapitulates human disease, we performed a high resolution longitudinal analysis of renal disease progression in ZSF1 rats spanning from early disease to end stage renal disease. Analyses included metabolic endpoints, renal histology and ultrastructure, evaluation of a urinary biomarker of fibrosis, and transcriptome analysis of glomerular-enriched tissue over the course of disease. Our findings support the translational value of the ZSF1 rat model, and are provided here to assist researchers in the determination of the model’s suitability for testing a particular mechanism of interest, the design of therapeutic intervention studies, and the identification of new targets and biomarkers for type 2 diabetic nephropathy. |
format | Online Article Text |
id | pubmed-5529026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55290262017-08-07 High resolution molecular and histological analysis of renal disease progression in ZSF1 fa/fa(CP) rats, a model of type 2 diabetic nephropathy Dower, Ken Zhao, Shanrong Schlerman, Franklin J. Savary, Leigh Campanholle, Gabriela Johnson, Bryce G. Xi, Li Nguyen, Vuong Zhan, Yutian Lech, Matthew P. Wang, Ju Nie, Qing Karsdal, Morten A. Genovese, Federica Boucher, Germaine Brown, Thomas P. Zhang, Baohong Homer, Bruce L. Martinez, Robert V. PLoS One Research Article ZSF1 rats exhibit spontaneous nephropathy secondary to obesity, hypertension, and diabetes, and have gained interest as a model system with potentially high translational value to progressive human disease. To thoroughly characterize this model, and to better understand how closely it recapitulates human disease, we performed a high resolution longitudinal analysis of renal disease progression in ZSF1 rats spanning from early disease to end stage renal disease. Analyses included metabolic endpoints, renal histology and ultrastructure, evaluation of a urinary biomarker of fibrosis, and transcriptome analysis of glomerular-enriched tissue over the course of disease. Our findings support the translational value of the ZSF1 rat model, and are provided here to assist researchers in the determination of the model’s suitability for testing a particular mechanism of interest, the design of therapeutic intervention studies, and the identification of new targets and biomarkers for type 2 diabetic nephropathy. Public Library of Science 2017-07-26 /pmc/articles/PMC5529026/ /pubmed/28746409 http://dx.doi.org/10.1371/journal.pone.0181861 Text en © 2017 Dower et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Dower, Ken Zhao, Shanrong Schlerman, Franklin J. Savary, Leigh Campanholle, Gabriela Johnson, Bryce G. Xi, Li Nguyen, Vuong Zhan, Yutian Lech, Matthew P. Wang, Ju Nie, Qing Karsdal, Morten A. Genovese, Federica Boucher, Germaine Brown, Thomas P. Zhang, Baohong Homer, Bruce L. Martinez, Robert V. High resolution molecular and histological analysis of renal disease progression in ZSF1 fa/fa(CP) rats, a model of type 2 diabetic nephropathy |
title | High resolution molecular and histological analysis of renal disease progression in ZSF1 fa/fa(CP) rats, a model of type 2 diabetic nephropathy |
title_full | High resolution molecular and histological analysis of renal disease progression in ZSF1 fa/fa(CP) rats, a model of type 2 diabetic nephropathy |
title_fullStr | High resolution molecular and histological analysis of renal disease progression in ZSF1 fa/fa(CP) rats, a model of type 2 diabetic nephropathy |
title_full_unstemmed | High resolution molecular and histological analysis of renal disease progression in ZSF1 fa/fa(CP) rats, a model of type 2 diabetic nephropathy |
title_short | High resolution molecular and histological analysis of renal disease progression in ZSF1 fa/fa(CP) rats, a model of type 2 diabetic nephropathy |
title_sort | high resolution molecular and histological analysis of renal disease progression in zsf1 fa/fa(cp) rats, a model of type 2 diabetic nephropathy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529026/ https://www.ncbi.nlm.nih.gov/pubmed/28746409 http://dx.doi.org/10.1371/journal.pone.0181861 |
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