COMP-angiopoietin-1 enhances skeletal muscle blood flow and insulin sensitivity in mice

Am J Physiol Endocrinol Metab. 2009 Aug;297(2):E402-9. doi: 10.1152/ajpendo.00122.2009. Epub 2009 Jun 2.

Abstract

To test whether chronic enhanced blood flow alters insulin-stimulated glucose uptake, we measured skeletal muscle glucose uptake in chow-fed and high-fat-fed mice injected with adenovirus containing modified angiopoietin-1, COMP-Ang1, via euglycemic-hyperinsulinemic clamp. Blood flow rates and platelet endothelial cell adhesion molecule-1 positive endothelial cells in the hindlimb skeletal muscle were elevated in COMP-Ang1 compared with control LacZ. Whole body glucose uptake and whole body glycogen/lipid synthesis were elevated in COMP-Ang1 compared with LacZ in chow diet. High-fat diet significantly reduced whole body glucose uptake and whole body glycolysis in LacZ mice, whereas high-fat-fed COMP-Ang1 showed a level of whole body glucose uptake that was comparable with chow-fed LacZ and showed increased glucose uptake compared with high-fat-fed LacZ. Glucose uptake and glycolysis in gastrocnemius muscle of chow-fed COMP-Ang1 were increased compared with chow-fed LacZ. High-fat diet-induced whole body insulin resistance in the LacZ was mostly due to approximately 40% decrease in insulin-stimulated glucose uptake in skeletal muscle. In contrast, COMP-Ang1 prevented diet-induced skeletal muscle insulin resistance compared with high-fat-fed LacZ. Akt phosphorylation in skeletal muscle was increased in COMP-Ang1 compared with LacZ in both chow-fed and high-fat-fed groups. These results suggest that increased blood flow by COMP-Ang1 increases insulin-stimulated glucose uptake and prevents high-fat diet-induced insulin resistance in skeletal muscle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Body Composition / drug effects
  • Cells, Cultured
  • Diet, Atherogenic
  • Dietary Fats / pharmacology
  • Humans
  • Insulin / pharmacology
  • Insulin Resistance* / physiology
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Muscle, Skeletal / blood supply*
  • Muscle, Skeletal / drug effects*
  • Muscle, Skeletal / metabolism
  • Oncogene Protein v-akt / metabolism
  • Phosphorylation / drug effects
  • Recombinant Fusion Proteins / pharmacology*
  • Regional Blood Flow / drug effects*

Substances

  • Blood Glucose
  • COMP-Ang1 fusion protein
  • Dietary Fats
  • Insulin
  • Recombinant Fusion Proteins
  • Oncogene Protein v-akt