TY - JOUR
T1 - Effect of short-term free fatty acids elevation on mitochondrial function in skeletal muscle of healthy individuals
AU - Chavez, Alberto O.
AU - Kamath, Subhash
AU - Jani, Rucha
AU - Sharma, Lokendra K.
AU - Monroy, Adriana
AU - Abdul-Ghani, Muhammad A.
AU - Centonze, Victoria E.
AU - Sathyanarayana, Padma
AU - Coletta, Dawn K.
AU - Jenkinson, Cristopher P.
AU - Bai, Yidong
AU - Folli, Franco
AU - DeFronzo, Ralph A.
AU - Tripathy, Devjit
N1 - Funding Information:
This study was funded in part by a GCRC CREF grant (D.T.) and National Institutes of Health Grant DK-24092 (R.A.D.) . Images were generated in the Core Optical Imaging Facility, which is supported by University of Texas Health Science Center at San Antonio , NIH-NCI P30 CA54174 (San Antonio Cancer Institute), NIH-NIA P30 AG013319 (Nathan Shock Center), and (NIH-NIA P01AG19316) . A.O.C. was supported by a Mentor-Based Postdoctoral Fellowship from the American Diabetes Association awarded to R.A.D.
PY - 2010/1
Y1 - 2010/1
N2 - Context: Mitochondrial dysfunction has been proposed as an underlying mechanism in the pathogenesis of insulin resistance and type 2 diabetes mellitus. Objective: To determine whether mitochondrial dysfunction plays a role in the free fatty acid (FFA)-induced impairment in insulin action in skeletal muscle of healthy subjects. Design: Eleven lean normal glucose tolerant individuals received 8 h lipid and saline infusion on separate days with a euglycemic insulin clamp during the last 2 h. Vastus lateralis muscle biopsies were performed at baseline and after 6 h lipid or saline infusion. Inner mitochondrial membrane potential (ψm) and mitochondrial mass were determined ex vivo by confocal microscopy. Results: Compared with saline infusion, lipid infusion reduced whole-body glucose uptake by 22% (P<0.05). ψm decreased by 33%(P<0.005) after lipid infusion and the decrement in ψm correlated with change in plasma FFA after lipid infusion (r = 0.753; P < 0.005). Mitochondrial content and morphology did not change after lipid infusion. No significant changes in genes expression, citrate synthase activity, and total ATP content were observed after either lipid or saline infusion. Conclusions: Short-term physiological increase in plasma FFA concentration in lean normal glucose tolerant subjects induces insulin resistance and impairs mitochondrial membrane potential but has no significant effects on mitochondrial content, gene expression, ATP content, or citrate synthase activity.
AB - Context: Mitochondrial dysfunction has been proposed as an underlying mechanism in the pathogenesis of insulin resistance and type 2 diabetes mellitus. Objective: To determine whether mitochondrial dysfunction plays a role in the free fatty acid (FFA)-induced impairment in insulin action in skeletal muscle of healthy subjects. Design: Eleven lean normal glucose tolerant individuals received 8 h lipid and saline infusion on separate days with a euglycemic insulin clamp during the last 2 h. Vastus lateralis muscle biopsies were performed at baseline and after 6 h lipid or saline infusion. Inner mitochondrial membrane potential (ψm) and mitochondrial mass were determined ex vivo by confocal microscopy. Results: Compared with saline infusion, lipid infusion reduced whole-body glucose uptake by 22% (P<0.05). ψm decreased by 33%(P<0.005) after lipid infusion and the decrement in ψm correlated with change in plasma FFA after lipid infusion (r = 0.753; P < 0.005). Mitochondrial content and morphology did not change after lipid infusion. No significant changes in genes expression, citrate synthase activity, and total ATP content were observed after either lipid or saline infusion. Conclusions: Short-term physiological increase in plasma FFA concentration in lean normal glucose tolerant subjects induces insulin resistance and impairs mitochondrial membrane potential but has no significant effects on mitochondrial content, gene expression, ATP content, or citrate synthase activity.
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U2 - 10.1210/jc.2009-1387
DO - 10.1210/jc.2009-1387
M3 - Article
C2 - 19864449
AN - SCOPUS:75149159121
SN - 0021-972X
VL - 95
SP - 422
EP - 429
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 1
ER -