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Am J Physiol Endocrinol Metab 288: E748-E752, 2005; doi:10.1152/ajpendo.00515.2004
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Physical training reverses defect in 3-ketoacid CoA-transferase activity in skeletal muscle of diabetic rats

Adil El Midaoui,1 Jean Louis Chiasson,2 Gilles Tancrède,1 and André Nadeau1

1Diabetes Research Unit, Research Center of Laval University Medical Center, Ste-Foy; and 2Research Group on Diabetes and Metabolic Regulation, Research Centre, Hotel-Dieu, Montreal, Quebec, Canada

Submitted 29 October 2004 ; accepted in final form 29 November 2004

To investigate one potential mechanism whereby physical training improves the plasma concentration of ketone bodies in experimental diabetes mellitus, we measured the activity of 3-ketoacid CoA-transferase, the key enzyme in the peripheral utilization of ketone bodies. Diabetes was induced with streptozotocin (50 mg/kg) and training carried out on a treadmill with a progressive 10-wk program. Diabetes resulted in an increase (P < 0.001) in plasma concentration of {beta}-hydroxybutyric acid in sedentary rats, which was partly reversed by training (P < 0.001). Diabetes was also associated with a decreased activity of 3-ketoacid CoA-transferase in gastrocnemius muscle. When expressed per total gastrocnemius, training increased the activity of 3-ketoacid CoA-transferase by 66% in nondiabetic rats (P < 0.001) and by 150% in diabetic rats (P < 0.001), the decrease present in diabetic rats being fully reversed by training. Simple linear regression between the log of 3-ketoacid CoA-transferase activity and the log of plasma {beta}-hydroxybutyric acid levels showed a statistically significant (r = 0.563, P < 0.001) negative correlation. The beneficial effects of training on plasma ketone bodies in diabetic rats are probably explained, at least in part, by an increase in ketone body utilization, mediated by an increase in skeletal muscle 3-ketoacid CoA-transferase activity.

{beta}-hydroxybutyric acid; gastrocnemius; streptozotocin diabetes; free fatty acids



Address for reprint requests and other correspondence: A. El Midaoui, Dept. of Physiology, Univ. of Montreal, Succursale Centre Ville, Montreal, QC, Canada, H3C 3J7 (E-mail: adil.el.midaoui{at}umontreal.ca)




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