Adriamycin nephropathy: A model of focal segmental glomerulosclerosis
ABSTRACT Adriamycin nephropathy (AN) is a rodent model of chronic kidney disease that has been studied extensively and has enabled a greater understanding of the processes underlying the progression of chronic proteinuric renal disease. AN is characterized by podocyte injury followed by glomeruloscl...
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Published in | Nephrology (Carlton, Vic.) Vol. 16; no. 1; pp. 30 - 38 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Melbourne, Australia
Blackwell Publishing Asia
01.01.2011
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Subjects | |
Online Access | Get full text |
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Summary: | ABSTRACT
Adriamycin nephropathy (AN) is a rodent model of chronic kidney disease that has been studied extensively and has enabled a greater understanding of the processes underlying the progression of chronic proteinuric renal disease. AN is characterized by podocyte injury followed by glomerulosclerosis, tubulointerstitial inflammation and fibrosis. Genetic studies have demonstrated a number of loci that alter both risk and severity of renal injury induced by Adriamycin. Adriamycin‐induced renal injury has been shown in numerous studies to be modulated by both non‐immune and immune factors, and has facilitated further study of mechanisms of tubulointerstitial injury. This review will outline the pharmacological behaviour of Adriamycin, and describe in detail the model of AN, including its key structural characteristics, genetic susceptibility and pathogenesis.
This review provides a comprehensive overview of experimental adriamycin nephropathy, including analysis of its strengths and weaknesses, pathogenic mechanisms and practical advice on how best to perform this animal model of chronic kidney disease. |
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Bibliography: | ArticleID:NEP1383 istex:BC1C2B17538E6979F7104BED9DCE5540062E716F ark:/67375/WNG-PWTVG7G8-0 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 1320-5358 1440-1797 |
DOI: | 10.1111/j.1440-1797.2010.01383.x |