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| Research article summary (published 29 Sep 2009): |
Effect of the HMG-CoA reductase inhibitor rosuvastatin on early chronic kidney injury in obese zucker rats fed with an atherogenic diet.
Full Abstract
The obese Zucker rat (OZR) spontaneously develops hyperlipidemia, insulin resistance, and microalbuminuria. In this study, the initial metabolic, functional, and glomerular pathology in young OZR fed with an atherogenic diet resembles the characteristics of metabolic syndrome. Hyperlipidemia and other metabolic derangement cause early glomerular damage in OZR by 10 weeks of age, before overt diabetes is developed. Consequently, the effects of potential interventions should also be evaluated at the young age. In OZR fed with an atherogenic high-fat diet, low (5 mg/kg) and high (20 mg/kg) dosages of rosuvastatin started at 5 weeks and maintained for 10 weeks induced a significant improvement in metabolic abnormalities, blood pressure, and renal function, including microalbuminuria. The low dose of rosuvastatin significantly decreased mesangial expansion, and the high dose exerted a marked protective effect on the development of both glomerular hypertrophy and mesangial expansion. The statin also attenuated the inflammatory expression in the kidney cortex.
Author information
Author/s: Reisin, Efrain (E); Ebenezer, Philip J (PJ); Liao, Jie (J); Lee, Benjamin S (BS); Larroque, Michelle (M); Hu, Xuejiao (X); Aguilar, Erwin A (EA); Morse, Stephen A (SA); Francis, Joseph (J);
Affiliation: Section of Nephrology and Hypertension, Department of Internal Medicine, Louisiana State University Health Sciences Center, New Orleans, Louisiana 70112, USA. ereisi(-atsign-)lsuhsc.edu
Journal and publication information
Publication Type: Journal Article
Journal: The American journal of the medical sciences (Am J Med Sci), published in United States. (Language: eng)
Reference: 2009-Oct; vol 338 (issue 4) : pp 301-9
Dates: Created 2009/10/14; Completed 2009/10/26;
PMID: 19826320, status: MEDLINE (last retrieval date: 10/26/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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