Effects of physical activity and weight loss on skeletal muscle mitochondria and relationship with glucose control in type 2 diabetes
FGS Toledo, EV Menshikova, VB Ritov, K Azuma… - Diabetes, 2007 - diabetesjournals.org
FGS Toledo, EV Menshikova, VB Ritov, K Azuma, Z Radikova, J DeLany, DE Kelley
Diabetes, 2007•diabetesjournals.orgOBJECTIVE—Reduced mitochondrial capacity in skeletal muscle occurs in type 2 diabetic
patients and in those at increased risk for this disorder, but the extent to which mitochondrial
dysfunction in type 2 diabetic patients is remediable by physical activity and weight loss
intervention is uncertain. We sought to address whether an intervention of daily moderate-
intensity exercise combined with moderate weight loss can increase skeletal muscle
mitochondrial content in type 2 diabetic patients and to address the relationship with …
patients and in those at increased risk for this disorder, but the extent to which mitochondrial
dysfunction in type 2 diabetic patients is remediable by physical activity and weight loss
intervention is uncertain. We sought to address whether an intervention of daily moderate-
intensity exercise combined with moderate weight loss can increase skeletal muscle
mitochondrial content in type 2 diabetic patients and to address the relationship with …
OBJECTIVE— Reduced mitochondrial capacity in skeletal muscle occurs in type 2 diabetic patients and in those at increased risk for this disorder, but the extent to which mitochondrial dysfunction in type 2 diabetic patients is remediable by physical activity and weight loss intervention is uncertain. We sought to address whether an intervention of daily moderate-intensity exercise combined with moderate weight loss can increase skeletal muscle mitochondrial content in type 2 diabetic patients and to address the relationship with amelioration of insulin resistance and hyperglycemia.
RESEARCH DESIGN AND METHODS— Muscle biopsies were obtained before and after a 4-month intervention to assess mitochondrial morphology, mitochondrial DNA content, and mitochondrial enzyme activities. Glucose control, body composition, aerobic fitness, and insulin sensitivity were measured.
RESULTS— In response to a weight loss of 7.1 ± 0.8% and a 12 ± 1.6% improvement in Vo2max (P < 0.05), insulin sensitivity improved by 59 ± 21% (P < 0.05). There were significant increases in skeletal muscle mitochondrial density (by 67 ± 17%, P < 0.01), cardiolipin content (55 ± 17%, P < 0.01), and mitochondrial oxidation enzymes. Energy expenditure during physical activity correlated with the degree of improvement in insulin sensitivity (r = 0.84, P < 0.01), and, in turn, improvement in mitochondrial content was a strong correlate of intervention-induced improvement in A1C and fasting plasma glucose.
CONCLUSIONS— Intensive short-term lifestyle modifications can restore mitochondrial content and functional capacity in skeletal muscle in type 2 diabetic patients. The improvement in the oxidative capacity of skeletal muscle may be a key component mediating salutary effects of lifestyle interventions on hyperglycemia and insulin resistance.
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