Akt, AS160, metabolic risk factors and aerobic fitness in middle-aged women

Autor/innen

  • Itamar Levinger Institute of Sport, Exercise and Active Living, School of Sport and Exercise Science, Victoria University, Melbourne, AUSTRALIA Autor/in
  • Kirsten F. Howlett School of Exercise and Nutrition Sciences, Deakin University, Melbourne, AUSTRALIA Autor/in
  • Jonathan Peake The University of Queensland, School of Human Movement Studies, Brisbane AUSTRALIA Autor/in
  • Andrew Garnham School of Exercise and Nutrition Sciences, Deakin University, Melbourne, AUSTRALIA Autor/in
  • David L. Hare University of Melbourne and the Department of Cardiology, Austin Health, Melbourne, AUSTRALIA Autor/in
  • George Jerums University of Melbourne and the Department of Endocrinology, Austin Health, Melbourne, AUSTRALIA Autor/in
  • Steve Selig Institute of Sport, Exercise and Active Living, School of Sport and Exercise Science, Victoria University, Melbourne, AUSTRALIA Autor/in
  • Craig Goodman Institute of Sport, Exercise and Active Living, School of Sport and Exercise Science, Victoria University, Melbourne, AUSTRALIA Autor/in

DOI:

https://doi.org/10.22029/eir.2010.1654

Schlagwörter:

INSULIN-RECEPTOR SUBSTRATE-1, SKELETAL-MUSCLE, GLUCOSE-TRANSPORT, KINASE-ACTIVITY, RESISTANCE, PHOSPHORYLATION, INFLAMMATION, ALPHA, INDIVIDUALS

Abstract

Aims: This study investigated the association between the basal (rest) insulin-signaling proteins, Akt, and the Akt substrate AS160, metabolic risk factors, inflammatory markers and aerobic fitness, in middle-aged women with varying numbers of metabolic risk factors for type 2 diabetes. Methods: Sixteen women (n = 16) aged 51.3+/-5.1 (mean +/-SD) years provided muscle biopsies and blood samples at rest. In addition, anthropometric characteristics and aerobic power were assessed and the number of metabolic risk factors for each participant was determined (IDF criteria). Results: The mean number of metabolic risk factors was 1.6+/-1.2. Total Akt was negatively correlated with IL-1 beta (r = -0.45, p = 0.046), IL-6 (r = -0.44, p = 0.052) and TNF-alpha (r = -0.51, p = 0.025). Phosphorylated AS160 was positively correlated with HDL (r = 0.58, p = 0.024) and aerobic fitness (r = 0.51, p = 0.047). Furthermore, a multiple regression analysis revealed that both HDL (t = 2.5, p = 0.032) and VO(2peak) (t = 2.4, p = 0.037) were better predictors for phosphorylated AS160 than TNF-alpha or IL-6 (p>0.05). Conclusions: Elevated inflammatory markers and increased metabolic risk factors may inhibit insulin-signaling protein phosphorylation in middle-aged women, thereby increasing insulin resistance under basal conditions. Furthermore, higher HDL and fitness levels are associated with an increased AS160 phosphorylation, which may in turn reduce insulin resistance.

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Veröffentlicht

2010-12-31

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Articles