Atorvastatin improves insulin sensitivity in mice with obesity induced by monosodium glutamate

Aim: To examine the mechanisms underlying the effects of atorvastatin on glucose and lipid metabolism.

Methods: Mice with Insulin resistance and obesity induced by monosodium glutamate (MSG) were used. Atorvastatin (80 mg.kg(-1).d(-1)) or vehicle control treatment was given orally once a day for 30 days. Plasma levels of total Cholesterol, triglycerides, low-density lipoprotein Cholesterol (LDL-C), high-density lipoprotein Cholesterol (HDL-C), and free fatty acids were monitored. Serum Insulin and glucose concentrations were used to calculate the Insulin resistance index and Insulin sensitivity index using a homeostasis model. Body length, waistline circumference, intraperitoneal adipose tissue mass, and total body mass were measured. Semi-quantitative RT-PCR and Western analysis were used to determine the expression of inflammatory factors and proteins involved in inflammation signaling pathways.

Results: Atorvastatin improved Insulin sensitivity, ameliorated glucose tolerance, and decreased plasma levels of total Cholesterol, triglycerides, LDL-C, HDL-C and free fatty acids. Semi-quantitative RT-PCR and Western analysis revealed increased expression of interleukin 6 (IL-6) and tumor necrosis factor alpha (TNF-alpha) in serum and adipose tissue in MSG obese mice. Atorvastatin treatment decreased expression of IL-6, TNF-alpha, nuclear factor kappaB (NF-kappaB) and I-kappa-B (IkappaB) kinase-beta, but increased the expression of IkappaB, in adipose tissue.

Conclusion: Atorvastatin is a potential candidate for the prevention and therapy of diseases associated with Insulin resistance such as type 2 diabetes mellitus and Cardiovascular Disease. One possible mechanism underlying the effects of atorvastatin on glucose and lipid metabolism may be to ameliorate a state of chronic inflammation.