as-605240 and Obesity

as-605240 has been researched along with Obesity* in 1 studies

Other Studies

1 other study(ies) available for as-605240 and Obesity

ArticleYear
Blockade of class IB phosphoinositide-3 kinase ameliorates obesity-induced inflammation and insulin resistance.
    Proceedings of the National Academy of Sciences of the United States of America, 2011, Apr-05, Volume: 108, Issue:14

    Obesity and insulin resistance, the key features of metabolic syndrome, are closely associated with a state of chronic, low-grade inflammation characterized by abnormal macrophage infiltration into adipose tissues. Although it has been reported that chemokines promote leukocyte migration by activating class IB phosphoinositide-3 kinase (PI3Kγ) in inflammatory states, little is known about the role of PI3Kγ in obesity-induced macrophage infiltration into tissues, systemic inflammation, and the development of insulin resistance. In the present study, we used murine models of both diet-induced and genetically induced obesity to examine the role of PI3Kγ in the accumulation of tissue macrophages and the development of obesity-induced insulin resistance. Mice lacking p110γ (Pik3cg(-/-)), the catalytic subunit of PI3Kγ, exhibited improved systemic insulin sensitivity with enhanced insulin signaling in the tissues of obese animals. In adipose tissues and livers of obese Pik3cg(-/-) mice, the numbers of infiltrated proinflammatory macrophages were markedly reduced, leading to suppression of inflammatory reactions in these tissues. Furthermore, bone marrow-specific deletion and pharmacological blockade of PI3Kγ also ameliorated obesity-induced macrophage infiltration and insulin resistance. These data suggest that PI3Kγ plays a crucial role in the development of both obesity-induced inflammation and systemic insulin resistance and that PI3Kγ can be a therapeutic target for type 2 diabetes.

    Topics: Adipose Tissue; Animals; Class Ib Phosphatidylinositol 3-Kinase; Flow Cytometry; Gene Expression Profiling; Histological Techniques; Inflammation; Insulin Resistance; Liver; Macrophages; Mice; Mice, Knockout; Obesity; Phosphoinositide-3 Kinase Inhibitors; Quinoxalines; Thiazolidinediones

2011