Home LiteratureArticle Details
PMID: 12372761 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Obstructive nephropathy and renal fibrosis.

American journal of physiology. Renal physiology ·Vol. 283 ·No. 5 ·2002-11-00 ·Pages F861-75

Klahr S, Morrissey J

Abstract

Interstitial fibrosis has a major role in the progression of renal diseases. Several animal models are available for the study of renal fibrosis. The models of aminonucleoside-induced nephrotic syndrome, cyclosporin nephrotoxicity, and passive Heyman nephritis are characterized by molecular and cellular events similar to those that occur in obstructive nephropathy. Additionally, inhibition of angiotensin-converting enzyme exerts salutary effects on the progression of renal fibrosis in obstructive nephropathy. Unilateral ureteral obstruction (UUO) has emerged as an important model for the study of the mechanisms of renal fibrosis and also for the evaluation of the impact of potential therapeutic approaches to ameliorate renal disease. Many quantifiable pathophysiological events occur over the span of 1 wk of UUO, making this an attractive model for study. This paper reviews some of the ongoing studies that utilized a rodent model of UUO. Some of the findings of the animal model have been compared with observations made in patients with obstructive nephropathy. Most of the evidence suggests that the rodent model of UUO is reflective of human renal disease processes.

MeSH Terms
Animals Fibrosis Humans Kidney Diseases/metabolism,pathology,physiopathology Ureteral Obstruction/metabolism,pathology,physiopathology
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Klahr Saulo
Department of Internal Medicine, Washington University School of Medicine at Barnes-Jewish Hospital, St. Louis, Missouri 63110-1092, USA. sklahr@im.wustl.edu
Morrissey Jeremiah
Article Info
Journal
American journal of physiology. Renal physiology
Abbr.
Am J Physiol Renal Physiol
ISSN
1931-857X
Published
2002-11-00
Pages
F861-75
Language
English
Region
United States
NLM ID
100901990
Subset
IM
Grants
NIDDK NIH HHS · DK-09976 · United States
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