Effect of roux-en-Y gastric bypass and laparoscopic adjustable gastric banding on branched-chain amino acid metabolism
- Faidon Magkos, PhD1,
- David Bradley, MD1,
- George G. Schweitzer, PhD1,
- Brian N. Finck, PhD1,
- J. Christopher Eagon, MD1,
- Olga Ilkayeva, PhD2,
- Christopher B. Newgard, PhD2 and
- Samuel Klein, MD1
- 1Center for Human Nutrition and Atkins Center of Excellence in Obesity Medicine, Washington University School of Medicine, St. Louis, MO.
- 2Sarah W. Stedman Nutrition and Metabolism Center, Departments of Pharmacology and Cancer Biology and Medicine, Duke University School of Medicine, Durham, NC.
- Corresponding author: Samuel Klein, E-mail:
It has been hypothesized that a greater decline in circulating branched-chain amino acids (BCAAs) after weight loss induced by roux-en-Y gastric bypass (RYGB) surgery than after calorie restriction alone has independent effects on glucose homeostasis, possibly by decreased signaling through the mammalian target of rapamycin (mTOR). We evaluated plasma BCAA and their C3 and C5 acylcarnitine metabolites, muscle mTOR phosphorylation, and insulin sensitivity (insulin-stimulated glucose rate of disappearance [Rd]) in obese subjects before and after ∼20% weight loss induced by RYGB (n=10, BMI 45.6±6.7 kg/m2) or laparoscopic adjustable gastric banding (LAGB; n=10, BMI 46.5±8.8 kg/m2). Weight loss increased insulin-stimulated glucose Rd by ∼55%, decreased total plasma BCAA and C3 and C5 acylcarnitine concentrations by 20-35%, and did not alter mTOR phosphorylation; no differences were detected between surgical groups (all P-values for interaction >0.05). Insulin-stimulated glucose Rd correlated negatively with plasma BCAAs and with C3 and C5 acylcarnitine concentrations (r-values: -0.56 to -0.75, P<0.05). These data demonstrate that weight loss induced by either LAGB or RYGB causes the same decline in circulating BCAAs and their C3 and C5 acylcarnitine metabolites. Plasma BCAA concentration is negatively associated with skeletal muscle insulin sensitivity, but the mechanism(s) responsible for this relationship is not known.
- Received February 3, 2013.
- Accepted April 16, 2013.
- © 2013 by the American Diabetes Association.
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