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Comparative study between atorvastatin and losartan on high fat diet‐induced type 2 diabetes mellitus in rats

Abstract

Obesity is often associated with chronic inflammatory state which contributes to the development of insulin resistance (IR) and type‐2 diabetes mellitus (T2DM). This study investigated the effects of single and combined administration of atorvastatin (ATOR, lipid lowering drug) and losartan (LOS, angiotensin receptor antagonist) on metabolic disorders and inflammatory status that are implicated in development of T2DM with the use of pioglitazone (PIO) as a standard antidiabetic drug. T2DM was induced in male rats by high fat diet (HFD) feeding for sixteen weeks. Oral administrations of ATOR (10 mg/kg), LOS (20 mg/kg), PIO (3 mg/kg), their binary combinations, or vehicle were started in the last four weeks. Fasting serum glucose, oral glucose tolerance, fasting serum insulin, IR, serum lipid profile, serum TNF‐α and body composition index were determined. Results showed that all drugs and their combinations had positive impact effect on all measured parameters, and better results were achieved from binary drug combinations than administration of each drug alone. Combination of PIO with either ATOR or LOS provided better improvements on T2DM‐associated metabolic abnormalities and inflammatory status with respect to each drug alone. However, the most pronounced effects of drugs and their combinations regarding the above parameters were attributed to LOS+PIO combination. In conclusion, this study indicates that combination of ATOR+PIO and, in particular, LOS+PIO can be used as promising effective therapies in the management of HFD‐induced T2DM. This concept may be attributed to the combined effects of the respective monotherapies to improve lipid profile, insulin sensitivity and TNF‐α level.

Autoren:   Ahmed A. Mourad, Gehan H. Heeba, Ashraf Taye, Mohamed A. El‐Moselhy
Journal:   Fundamental & Clinical Pharmacology
Jahrgang:   2012
Seiten:   n/a
DOI:   10.1111/j.1472-8206.2012.01048.x
Erscheinungsdatum:   21.05.2012

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