TY - JOUR
T1 - Plasma amino acids stimulate uncoupled respiration of muscle subsarcolemmal mitochondria in lean but not obese humans
AU - Kras, Katon A.
AU - Hoffman, Nyssa
AU - Roust, Lori R.
AU - Patel, Shivam H.
AU - Carroll, Chad C.
AU - Katsanos, Christos
N1 - Funding Information:
Financial Support: The present study was supported by the National Institutes of Health/National Institute of Diabetes and Digestive and Kidney Diseases (Grant R01DK094062 to C.S.K.).
Publisher Copyright:
Copyright © 2017 Endocrine Society.
PY - 2017
Y1 - 2017
N2 - Context: Obesity is associated with mitochondrial dysfunction in skeletal muscle. Increasing the plasma amino acid (AA) concentrations stimulates mitochondrial adenosine triphosphate (ATP) production in lean individuals. Objective: To determine whether acute elevation in plasma AAs enhances muscle mitochondrial respiration and ATP production in subsarcolemmal (SS) and intermyofibrillar (IMF) mitochondria in obese adults. Design: Assessment of SS and IMF mitochondrial function during saline (i.e., control) and AA infusions. Participants: Eligible participants were healthy lean (body mass index, 25 kg/m2; age, 37 63 years; n = 10) and obese (body mass index .30 kg/m2; age 35 6 3 years; n = 11) subjects. Intervention: Single trial of saline infusion followed by AA infusion. SS and IMF mitochondria were isolated from muscle biopsies collected at the end of the saline and AA infusions. Main Outcomes: Mitochondrial respiration and ATP production. Results: AA infusion increased adenosine 50-diphosphate (ADP)-stimulated respiration and ATP production rates of SS mitochondria in the lean (P,0.05), but not obese, subjects. Furthermore, AA infusion increased the uncoupled (i.e., non-ADP-stimulated) respiration of SS mitochondria in the lean subjects only (P , 0.05). AA infusion had no effect on any of these parameters in IMF mitochondria in either lean or obese subjects (P . 0.05). Conclusions: Increasing the plasmaAAconcentrations enhances the capacity for respiration and ATP production of muscle SS, but not IMF, mitochondria in lean individuals, in parallel with increases in uncoupled respiration. However, neither of these parameters increases in muscle SS or IMF mitochondria in obese individuals.
AB - Context: Obesity is associated with mitochondrial dysfunction in skeletal muscle. Increasing the plasma amino acid (AA) concentrations stimulates mitochondrial adenosine triphosphate (ATP) production in lean individuals. Objective: To determine whether acute elevation in plasma AAs enhances muscle mitochondrial respiration and ATP production in subsarcolemmal (SS) and intermyofibrillar (IMF) mitochondria in obese adults. Design: Assessment of SS and IMF mitochondrial function during saline (i.e., control) and AA infusions. Participants: Eligible participants were healthy lean (body mass index, 25 kg/m2; age, 37 63 years; n = 10) and obese (body mass index .30 kg/m2; age 35 6 3 years; n = 11) subjects. Intervention: Single trial of saline infusion followed by AA infusion. SS and IMF mitochondria were isolated from muscle biopsies collected at the end of the saline and AA infusions. Main Outcomes: Mitochondrial respiration and ATP production. Results: AA infusion increased adenosine 50-diphosphate (ADP)-stimulated respiration and ATP production rates of SS mitochondria in the lean (P,0.05), but not obese, subjects. Furthermore, AA infusion increased the uncoupled (i.e., non-ADP-stimulated) respiration of SS mitochondria in the lean subjects only (P , 0.05). AA infusion had no effect on any of these parameters in IMF mitochondria in either lean or obese subjects (P . 0.05). Conclusions: Increasing the plasmaAAconcentrations enhances the capacity for respiration and ATP production of muscle SS, but not IMF, mitochondria in lean individuals, in parallel with increases in uncoupled respiration. However, neither of these parameters increases in muscle SS or IMF mitochondria in obese individuals.
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U2 - 10.1210/jc.2017-01201
DO - 10.1210/jc.2017-01201
M3 - Article
C2 - 29029131
AN - SCOPUS:85038254428
SN - 0021-972X
VL - 102
SP - 4515
EP - 4525
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 12
ER -