Study of Changes in Skeletal Muscle After Caloric Restriction

We hypothesize that in a setting of surgically-induced weight loss decrements in select DAGs result in improved glucose utilization, altered insulin signaling and decreased inflammatory responses. We propose to examine the impact of molecular DAG species accumulation on glucose utilization, insulin signaling and inflammation in skeletal muscle from morbidly obese subjects before/after 10% weight loss facilitated by Roux-en-Y Gastric Bypass (RYGB). We will compare these results to those from a control, normal weight cohort

The detected differences in DAG molecular species, insulin action, inflammatory responses between normal and obese subjects (before/after weight loss) will emphasize pathways coordinately altered as a consequence of adiposity and RYGB surgery. The primary endpoints for this study will be: Insulin sensitivity (glucose Rd, insulin levels, DAG mass, DAG species amounts).Secondary endpoints will be: FFA levels, inflammatory cytokine production, and insulin signaling in skeletal muscle.

Inclusion criteria

• For Normal Weight Subjects:

• Age 21-65 years
• BMI of 21 to 27 kg/m2
• Normal glucose tolerance as determined by OGTT on day of screening
• No family history of diabetes
• For Morbidly Obese Subjects:

• Age 21-65 years
• BMI of 30 to 65 kg/m2
• Scheduled for Roux-en-Y gastric bypass at Vanderbilt Medical Center
• Insulin resistant as determined by OGTT on day of screening

Exclusion criteria

(for all subjects):

• Clinically significant heart disease
• Clinically significant hepatic or renal disease
• Pregnancy
• Breastfeeding
• Any abnormality that would preclude safe completion of study
• Use of statins
• Use of thiazide or furosemide diuretics, beta blockers, or other chronic medications with known adverse effects on glucose tolerance levels unless subject has been on stable dose of such medications for the past 3 months before entering the study