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Vol. 28, No. 4, 2008
Issue release date: June 2008
Section title: Original Report: Laboratory Investigation
Am J Nephrol 2008;28:598–606
(DOI:10.1159/000116885)

PPAR-Alpha Agonist Fenofibrate Induces Renal CYP Enzymes and Reduces Blood Pressure and Glomerular Hypertrophy in Zucker Diabetic Fatty Rats

Zhao X. · Li L.-Y.
Department of Physiology, Morehouse School of Medicine, Atlanta, Ga., USA

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Article / Publication Details

First-Page Preview
Abstract of Original Report: Laboratory Investigation

Received: 11/13/2007
Accepted: 12/22/2007
Published online: 2/14/2008
Issue release date: June 2008

Number of Print Pages: 9
Number of Figures: 5
Number of Tables: 1

ISSN: 0250-8095 (Print)
eISSN: 1421-9670 (Online)

For additional information: http://www.karger.com/AJN

Abstract

We have previously shown that fenofibrate, a peroxisome proliferator-activated receptor-α activator, increases renal cytochrome P450 (CYP)-derived eicosanoids and improves endothelial function in pre-diabetic obese rats. The present study was designed to explore the efficacy of fenofibrate on blood pressure and renal injury in the advanced stage of type-2 diabetes. 26-week-old male Zucker diabetic fatty rats (ZDF) were fed fenofibrate (100 mg/kg/day) for 6 weeks. Chronic treatment with fenofibrate normalized systolic blood pressure and reduced glomerular size by 19% in diabetic rats. Western blot and fluorescent immunostaining revealed that the over-expression of collagen type IV and α-smooth muscle actin was significantly attenuated in the kidney of fenofibrate-treated ZDF (F-ZDF) rats. In addition, fenofibrate administration dramatically decreased the cyclin D1 protein level in the kidney of diabetic rats. In contrast, renal CYP2C23 and CYP4A proteins were significantly increased in F-ZDF rats. These fenofibrate effects were observed in the absence of significant changes in glucose, insulin or lipid levels. Taken together, our results demonstrate that fenofibrate may lower blood pressure and attenuate glomerular hypertrophy and collagen accumulation through the downregulation of cyclin D1 and upregulation of CYP monooxygenases in the late stage of type-2 diabetes.

© 2008 S. Karger AG, Basel


  

Author Contacts

Dr. Xueying Zhao
Department of Physiology, Morehouse School of Medicine
Atlanta, GA 30310 (USA)
Tel. +1 404 752 1902, Fax +1 404 752 1045
E-Mail xzhao@msm.edu

  

Article Information

Received: November 13, 2007
Accepted: December 22, 2007
Published online: February 14, 2008
Number of Print Pages : 9
Number of Figures : 5, Number of Tables : 1, Number of References : 42

  

Publication Details

American Journal of Nephrology

Vol. 28, No. 4, Year 2008 (Cover Date: June 2008)

Journal Editor: Bakris, G. (Chicago, Ill.)
ISSN: 0250–8095 (Print), eISSN: 1421–9670 (Online)

For additional information: http://www.karger.com/AJN


Article / Publication Details

First-Page Preview
Abstract of Original Report: Laboratory Investigation

Received: 11/13/2007
Accepted: 12/22/2007
Published online: 2/14/2008
Issue release date: June 2008

Number of Print Pages: 9
Number of Figures: 5
Number of Tables: 1

ISSN: 0250-8095 (Print)
eISSN: 1421-9670 (Online)

For additional information: http://www.karger.com/AJN


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