prostaglandin-d2 and Glucose-Intolerance

The steroid receptor coactivator 1 (SRC1) regulates key metabolic pathways, including glucose homeostasis. SRC1(-/-) mice have decreased hepatic expression of gluconeogenic enzymes and a reduction in the rate of endogenous glucose production (EGP). We sought to determine whether decreasing hepatic and adipose SRC1 expression in normal adult rats would alter glucose homeostasis and insulin action. Regular chow-fed and high-fat-fed male Sprage-Dawley rats were treated with an antisense oligonucleotide (ASO) against SRC1 or a control ASO for 4 wk, followed by metabolic assessments. SRC1 ASO did not alter basal EGP or expression of gluconeogenic enzymes. Instead, SRC1 ASO increased insulin-stimulated whole body glucose disposal by ~30%, which was attributable largely to an increase in insulin-stimulated muscle glucose uptake. This was associated with an approximately sevenfold increase in adipose expression of lipocalin-type prostaglandin D2 synthase, a previously reported regulator of insulin sensitivity, and an approximately 70% increase in plasma PGD2 concentration. Muscle insulin signaling, AMPK activation, and tissue perfusion were unchanged. Although GLUT4 content was unchanged, SRC1 ASO increased the cleavage of tether-containing UBX domain for GLUT4, a regulator of GLUT4 translocation. These studies point to a novel role of adipose SRC1 as a regulator of insulin-stimulated muscle glucose uptake.

Topics: Adipose Tissue; Animals; Biological Transport; Diet, High-Fat; Enzyme Inhibitors; Gene Expression Regulation, Enzymologic; Glucose Intolerance; Glucose Transporter Type 4; Insulin Resistance; Intracellular Signaling Peptides and Proteins; Intramolecular Oxidoreductases; Lipocalins; Liver; Male; Muscle, Skeletal; Nuclear Receptor Coactivator 1; Oligodeoxyribonucleotides, Antisense; Phosphoenolpyruvate Carboxykinase (GTP); Prostaglandin D2; Protein Interaction Domains and Motifs; Proteolysis; Rats, Sprague-Dawley