Cargando…
Renal disease pathophysiology and treatment: contributions from the rat
The rat has classically been the species of choice for pharmacological studies and disease modeling, providing a source of high-quality physiological data on cardiovascular and renal pathophysiology over many decades. Recent developments in genome engineering now allow us to capitalize on the wealth...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5200898/ https://www.ncbi.nlm.nih.gov/pubmed/27935823 http://dx.doi.org/10.1242/dmm.027276 |
_version_ | 1782489261372604416 |
---|---|
author | Mullins, Linda J. Conway, Bryan R. Menzies, Robert I. Denby, Laura Mullins, John J. |
author_facet | Mullins, Linda J. Conway, Bryan R. Menzies, Robert I. Denby, Laura Mullins, John J. |
author_sort | Mullins, Linda J. |
collection | PubMed |
description | The rat has classically been the species of choice for pharmacological studies and disease modeling, providing a source of high-quality physiological data on cardiovascular and renal pathophysiology over many decades. Recent developments in genome engineering now allow us to capitalize on the wealth of knowledge acquired over the last century. Here, we review rat models of hypertension, diabetic nephropathy, and acute and chronic kidney disease. These models have made important contributions to our understanding of renal diseases and have revealed key genes, such as Ace and P2rx7, involved in renal pathogenic processes. By targeting these genes of interest, researchers are gaining a better understanding of the etiology of renal pathologies, with the promised potential of slowing disease progression or even reversing the damage caused. Some, but not all, of these target genes have proved to be of clinical relevance. However, it is now possible to generate more sophisticated and appropriate disease models in the rat, which can recapitulate key aspects of human renal pathology. These advances will ultimately be used to identify new treatments and therapeutic targets of much greater clinical relevance. |
format | Online Article Text |
id | pubmed-5200898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52008982017-01-13 Renal disease pathophysiology and treatment: contributions from the rat Mullins, Linda J. Conway, Bryan R. Menzies, Robert I. Denby, Laura Mullins, John J. Dis Model Mech Review The rat has classically been the species of choice for pharmacological studies and disease modeling, providing a source of high-quality physiological data on cardiovascular and renal pathophysiology over many decades. Recent developments in genome engineering now allow us to capitalize on the wealth of knowledge acquired over the last century. Here, we review rat models of hypertension, diabetic nephropathy, and acute and chronic kidney disease. These models have made important contributions to our understanding of renal diseases and have revealed key genes, such as Ace and P2rx7, involved in renal pathogenic processes. By targeting these genes of interest, researchers are gaining a better understanding of the etiology of renal pathologies, with the promised potential of slowing disease progression or even reversing the damage caused. Some, but not all, of these target genes have proved to be of clinical relevance. However, it is now possible to generate more sophisticated and appropriate disease models in the rat, which can recapitulate key aspects of human renal pathology. These advances will ultimately be used to identify new treatments and therapeutic targets of much greater clinical relevance. The Company of Biologists Ltd 2016-12-01 /pmc/articles/PMC5200898/ /pubmed/27935823 http://dx.doi.org/10.1242/dmm.027276 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Review Mullins, Linda J. Conway, Bryan R. Menzies, Robert I. Denby, Laura Mullins, John J. Renal disease pathophysiology and treatment: contributions from the rat |
title | Renal disease pathophysiology and treatment: contributions from the rat |
title_full | Renal disease pathophysiology and treatment: contributions from the rat |
title_fullStr | Renal disease pathophysiology and treatment: contributions from the rat |
title_full_unstemmed | Renal disease pathophysiology and treatment: contributions from the rat |
title_short | Renal disease pathophysiology and treatment: contributions from the rat |
title_sort | renal disease pathophysiology and treatment: contributions from the rat |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5200898/ https://www.ncbi.nlm.nih.gov/pubmed/27935823 http://dx.doi.org/10.1242/dmm.027276 |
work_keys_str_mv | AT mullinslindaj renaldiseasepathophysiologyandtreatmentcontributionsfromtherat AT conwaybryanr renaldiseasepathophysiologyandtreatmentcontributionsfromtherat AT menziesroberti renaldiseasepathophysiologyandtreatmentcontributionsfromtherat AT denbylaura renaldiseasepathophysiologyandtreatmentcontributionsfromtherat AT mullinsjohnj renaldiseasepathophysiologyandtreatmentcontributionsfromtherat |