1. Lovastatin Enhances Paraoxonase Enzyme Activity and Quells low-density Lipoprotein Susceptibility to Oxidation in Type 2 Diabetic Nephropathy.
- Author
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Naghavi Behzad, Mohammad, Nezami, Nariman, Piri, Reza, Safa, Javid, Salari, Behzad, Rashtchi Zadeh, Nadereh, and Ghorbanihaghjo, Amir
- Subjects
TYPE 2 diabetes complications ,DIABETIC nephropathies ,ESTERASES ,LOW density lipoproteins ,OXIDATION-reduction reaction ,LOVASTATIN - Abstract
Background & Objectives: This study was done to investigate the effect of lovastatin therapy on paraoxonase 1 (PON1) and arylesterase (ARE) activities, and low-density lipoprotein cholesterol (LDL-C) susceptibility to oxidation in people with type 2 diabetic nephropathy (T2DN). Methods: Lovastatin (20 mg/day) was administered to 30 people with T2DN for 90 days and then withdrawn for 30 days. PON1 and ARE activities were measured by the spectrophotometric method. Susceptibility of LDL-C to oxidation was determined as the production of conjugated dienes. Results: After 90 days of lovastatin intervention, PON1 and ARE activities and LDL-C lag phase were significantly increased (p=0.004, 0.002, and b0.001). After 30 days of lovastatin withdrawal, PON1 and ARE activities and LDL-C lag phase had not changed significantly. Conclusion: Lovastatin therapy improves PON1 and ARE activities, and LDL-C susceptibility to oxidation. Despite withdrawal of lovastatin, PON1 and ARE activities, and LDL-C susceptibility to oxidation remain unchanged for a long period of time in people with T2DN. [ABSTRACT FROM AUTHOR]
- Published
- 2013