Exercise‐induced overexpression of key regulatory proteins involved in glucose uptake and metabolism in tetraplegic persons: molecular mechanism for improved glucose homeostasis

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Abstract
Complete spinal cord lesion leads to profound metabolic abnormalities and striking changes in muscle morphology. Here we assess the effects of electrically stimulated leg cycling (ESLC) on whole body insulin sensitivity, skeletal muscle glucose metabolism, and muscle fiber morphology in five tetraplegic subjects with complete C5-C7 lesions. Physical training (seven ESLC sessions/wk for 8 wk) increased whole body insulin-stimulated glucose uptake by 33±13%, concomitant with a 2.1-fold increase in insulin-stimulated (100 μU/ml) 3-O-methylglucose transport in isolated vastus lateralis muscle. Physical training led to a marked increase in protein expression of GLUT4 (378±85%), glycogen synthase (526±146%), and hexokinase II (204±47%) in vastus lateralis muscle, whereas phosphofructokinase expression (282±97%) was not significantly changed. Hexokinase II activity was significantly increased, whereas activity of phosphofructokinase, glycogen synthase, and citrate synthase was not changed after training. Muscle fiber type distribution and fiber area were markedly altered compared to able-bodied subjects before ESLC training, with no change noted in either parameter after ECSL training. In conclusion, muscle contraction improves insulin action on whole body and cellular glucose uptake in cervical cord-injured persons through a major increase in protein expression of key genes involved in the regulation of glucose metabolism. Furthermore, improvements in insulin action on glucose metabolism are independent of changes in muscle fiber type distribution.—Hjeltnes, N., Galuska, D., Björnholm, M., Aksnes, A.-K., Lannem, A., Zierath, J. R., Wallberg-Henriksson, H. Exercise-induced overexpression of key regulatory proteins involved in glucose uptake and metabolism in tetraplegic persons: molecular mechanism for improved glucose homeostasis. FASEB J. 12, 1701–1712 (1998)
Funding Information
  • Novo Nordisk Fonden
  • Centrum för idrottsforskning
  • Diabetesförbundet
  • Tore Nilsons Stiftelse för Medicinsk Forskning
  • Medicinska Forskningsrådet (9517, 11945, 11823, 12211)

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