AZ 242, a novel PPARα/γ agonist with beneficial effects on insulin resistance and carbohydrate and lipid metabolism in ob/ob mice and obese Zucker rats

Abstract

Abnormalities in fatty acid (333333333333382) metabolism underlie the development of insulin resistance and alterations in glucose metabolism, features characteristic of the metabolic syndrome and type 2 diabetes that can result in an increased risk of cardiovascular disease. We present pharmacodynamic effects of AZ 242, a novel peroxisome proliferator activated receptor (PPAR)α/γ agonist. AZ 242 dose-dependently reduced the hypertriglyceridemia, hyperinsulinemia, and hyperglycemia of ob/ob diabetic mice. Euglycemic hyperinsulinemic clamp studies showed that treatment with AZ 242 (1 μmol/kg/d) restored insulin sensitivity of obese Zucker rats and decreased insulin secretion. In vitro, in reporter gene assays, AZ 242 activated human PPARα and PPARγ with EC50 in the μmolar range. It also induced differentiation in 3T3-L1 cells, an established PPARγ effect, and caused up-regulation of liver fatty acid binding protein in HepG-2 cells, a PPARα-mediated effect. PPARα-mediated effects of AZ 242 in vivo were documented by induction of hepatic cytochrome P 450-4A in mice.The results indicate that the dual PPARα/γ agonism of AZ 242 reduces insulin resistance and has beneficial effects on FA and glucose metabolism. This effect profile could provide a suitable therapeutic approach to the treatment of type 2 diabetes, metabolic syndrome, and associated vascular risk factors.

Keywords

• hypertriglyceridemia
• peroxisome proliferator activated receptor
• type 2 diabetes