Impact of aerobic exercise training on age-related changes in insulin sensitivity and muscle oxidative capacity

Diabetes. 2003 Aug;52(8):1888-96. doi: 10.2337/diabetes.52.8.1888.

Abstract

Insulin resistance increases and muscle oxidative capacity decreases during aging, but lifestyle changes-especially physical activity-may reverse these trends. Here we report the effect of a 16-week aerobic exercise program (n = 65) or control activity (n = 37) performed by men and women aged 21-87 years on insulin sensitivity and muscle mitochondria. Insulin sensitivity, measured by intravenous glucose tolerance test, decreased with age (r = -0.32) and was related to abdominal fat content (r = -0.65). Exercise increased peak oxygen uptake (VO(2peak); 10%), activity of muscle mitochondrial enzymes (citrate synthase and cytochrome c oxidase, 45-76%) and mRNA levels of mitochondrial genes (COX4, ND4, both 66%) and genes involved in mitochondrial biogenesis (PGC-1alpha, 55%; NRF-1, 15%; TFAM, 85%). Exercise also increased muscle GLUT4 mRNA and protein (30-52%) and reduced abdominal fat (5%) and plasma triglycerides (25%). None of these changes were affected by age. In contrast, insulin sensitivity improved in younger people but not in middle-aged or older groups. Thus, the muscle mitochondrial response to 4 months of aerobic exercise training was similar in all age-groups, although the older people did not have an improvement in insulin sensitivity.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Aging / physiology*
  • Blood Glucose
  • Body Composition
  • Citrate (si)-Synthase / genetics
  • DNA-Binding Proteins / genetics
  • Diabetes Mellitus, Type 2 / physiopathology
  • Diabetes Mellitus, Type 2 / prevention & control
  • Exercise / physiology*
  • Female
  • Gene Expression
  • Glucose Intolerance / physiopathology
  • Glucose Intolerance / prevention & control*
  • Glucose Transporter Type 4
  • Humans
  • Insulin / blood
  • Insulin Resistance / physiology*
  • Lipids / blood
  • Male
  • Middle Aged
  • Mitochondria / enzymology
  • Mitochondrial Proteins*
  • Monosaccharide Transport Proteins / genetics
  • Muscle Proteins*
  • Muscle, Skeletal / metabolism*
  • NF-E2-Related Factor 1
  • Nuclear Proteins / genetics
  • Nuclear Respiratory Factor 1
  • Nuclear Respiratory Factors
  • Oxidation-Reduction
  • Prostaglandin-Endoperoxide Synthases / genetics
  • Trans-Activators / genetics
  • Transcription Factors / genetics

Substances

  • Blood Glucose
  • DNA-Binding Proteins
  • Glucose Transporter Type 4
  • Insulin
  • Lipids
  • Mitochondrial Proteins
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • NF-E2-Related Factor 1
  • NRF1 protein, human
  • Nuclear Proteins
  • Nuclear Respiratory Factor 1
  • Nuclear Respiratory Factors
  • SLC2A4 protein, human
  • TFAM protein, human
  • Trans-Activators
  • Transcription Factors
  • mitochondrial transcription factor A
  • peroxisome-proliferator-activated receptor-gamma coactivator-1
  • Prostaglandin-Endoperoxide Synthases
  • Citrate (si)-Synthase