Markers of Mitochondrial Biogenesis and Metabolism Are Lower in Overweight and Obese Insulin-Resistant Subjects

• Published in: The journal of clinical endocrinology and metabolism Vol. 92; no. 4; pp. 1467 - 1473
• Main Authors: Heilbronn, Leonie K., Gan, Seng Khee, Turner, Nigel, Campbell, Lesley V., Chisholm, Donald J.
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Oxford University Press 01.04.2007; Endocrine Society
• Subjects: Adipose Tissue - anatomy & histology; Adult; Aerobic capacity; Biological and medical sciences; Biomarkers; Body fat; Cardiorespiratory fitness; Citrate synthase; Cyclooxygenase 1 - genetics; Electron transport; Endocrinopathies; Enzymatic activity; Exercise; Fitness training programs; Fundamental and applied biological sciences. Psychology; Glucose Clamp Technique; Humans; Insulin - blood; Insulin Resistance; Male; Medical sciences; Metabolism; Mitochondria; Mitochondria, Muscle - genetics; Mitochondria, Muscle - metabolism; Mitochondria, Muscle - physiology; Mitochondrial DNA; Muscle, Skeletal - cytology; Muscle, Skeletal - pathology; Muscle, Skeletal - physiopathology; Obesity - physiopathology; Overweight - physiology; Oxygen Consumption; Physical fitness; Physical training; Protein turnover; Regression Analysis; Skeletal muscle; Vertebrates: endocrinology; Human; Resistance; Obesity; Pancreatic hormone; Mitochondria; Nutrition disorder; Biological marker; Metabolism; Insulin; Endocrinology; Nutritional status; Overweight
• ISSN: 0021-972X; 1945-7197
• DOI: 10.1210/jc.2006-2210

Background: Impaired mitochondrial function in skeletal muscle is implicated in the development of insulin resistance. However, potential differences in fatness and fitness may influence previous results. Methods: Subjects (n =18) were divided into insulin-sensitive (IS) and insulin-resistant (IR) groups by median glucose infusion rate during a hyperinsulinemic euglycemic clamp. Weight, VO2max (maximal aerobic capacity), and percentage body fat were measured before and after 6 continuous weeks of aerobic exercise training at 55–70% VO2max (40 min/session, 4 d/wk). Results: Age, percentage fat, and VO2max were not different between IS and IR groups at baseline. Expression of the nuclear encoded PGC1α and mitochondrial encoded gene COX1 were significantly lower in the IR group (P < 0.05). Citrate synthase activity and protein levels of subunits from complexes I and III of the respiratory chain were also lower in the IR group (P < 0.05). Insulin sensitivity and aerobic fitness were increased after exercise training in both groups (P < 0.001), and the expression of mitochondrial encoded genes CYTB and COX1 was also increased (P < 0.01). However, there was no change in PGC1α expression, mitochondrial enzyme activity, or protein levels of complexes of the respiratory chain in response to exercise in either group. Conclusion: This study confirms that IR men have reduced markers of mitochondrial metabolism, independent of fatness and fitness. Moderate exercise training did not alter these markers despite improving fitness and whole body insulin sensitivity. This study suggests that additional mechanisms may be involved in improving insulin resistance after exercise training in obese men.