Impairments in site-specific AS160 phosphorylation and effects of exercise training

Diabetes. 2013 Oct;62(10):3437-47. doi: 10.2337/db13-0229. Epub 2013 Jun 25.

Abstract

The purpose of this study was to determine if site-specific phosphorylation at the level of Akt substrate of 160 kDa (AS160) is altered in skeletal muscle from sedentary humans across a wide range of the adult life span (18-84 years of age) and if endurance- and/or strength-oriented exercise training could rescue decrements in insulin action and skeletal muscle AS160 phosphorylation. A euglycemic-hyperinsulinemic clamp and skeletal muscle biopsies were performed in 73 individuals encompassing a wide age range (18-84 years of age), and insulin-stimulated AS160 phosphorylation was determined. Decrements in whole-body insulin action were associated with impairments in insulin-induced phosphorylation of skeletal muscle AS160 on sites Ser-588, Thr-642, Ser-666, and phospho-Akt substrate, but not Ser-318 or Ser-751. Twelve weeks of endurance- or strength-oriented exercise training increased whole-body insulin action and reversed impairments in AS160 phosphorylation evident in insulin-resistant aged individuals. These findings suggest that a dampening of insulin-induced phosphorylation of AS160 on specific sites in skeletal muscle contributes to the insulin resistance evident in a sedentary aging population and that exercise training is an effective intervention for treating these impairments.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism*
  • Adult
  • Aged
  • Aged, 80 and over
  • Aging / metabolism*
  • Blotting, Western
  • Cross-Sectional Studies
  • Female
  • GTPase-Activating Proteins / metabolism*
  • Glucose Clamp Technique
  • Humans
  • Insulin / metabolism*
  • Male
  • Middle Aged
  • Muscle, Skeletal / metabolism*
  • Nuclear Proteins / metabolism*
  • Nuclear Receptor Interacting Protein 1
  • Phosphorylation
  • Physical Endurance
  • Resistance Training*
  • Sedentary Behavior
  • Serine
  • Signal Transduction
  • Threonine

Substances

  • Adaptor Proteins, Signal Transducing
  • GTPase-Activating Proteins
  • Insulin
  • Nuclear Proteins
  • Nuclear Receptor Interacting Protein 1
  • TBC1D4 protein, human
  • Threonine
  • Serine