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Am J Physiol Endocrinol Metab 294: E203-E213, 2008. First published November 14, 2007; doi:10.1152/ajpendo.00624.2007
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INVITED REVIEW

Determinants of intramyocellular triglyceride turnover: implications for insulin sensitivity

Cédric Moro, Sudip Bajpeyi, and Steven R. Smith

Pennington Biomedical Research Center, Molecular and Experimental Endocrinology Laboratory, Baton Rouge, Louisiana

Increased intramyocellular triglyceride (IMTG) content is found in both insulin-sensitive endurance-trained subjects and insulin-resistant obese/type 2 diabetic subjects. A high turnover rate of the IMTG pool in athletes is proposed to reduce accumulation of lipotoxic intermediates interfering with insulin signaling. IMTG turnover is a composite measure of the dynamic balance between lipolysis and lipid synthesis; both are influenced by mitochondrial fat oxidation and plasma free fatty acid availability. Therefore, more attention should be given to the factors controlling the rate of turnover of IMTG. In this review, particular attention has been given to muscle oxidative capacity, plasma free fatty acid availability, and IMTG hydrolysis (lipolysis) and synthesis. A higher oxidative, lipolytic, and lipid storage capacity in the muscle of endurance-trained subjects reflects a higher fractional turnover of the IMTG pool. Thus the co-localization of intermyofibrillar lipid droplets and mitochondria allows for a fine coupling of lipolysis of the IMTG pool to mitochondrial β-oxidation. Conversely, reduced oxidative capacity and a mismatch between IMTG lipolysis and β-oxidation might be detrimental to insulin sensitivity by generating several lipotoxic intermediates in sedentary populations including obese/type 2 diabetic subjects. Further studies are clearly required to better understand the relationship between the rate of turnover of IMTG and the accumulation of lipotoxic intermediates in the pathophysiology of insulin resistance.

lipolysis; exercise; lipid storage; type 2 diabetes; skeletal muscle



Address for reprint requests and other correspondence: S. R. Smith, Pennington Biomedical Research Center, 6400 Perkins Rd., Baton Rouge, LA 70808 (e-mail: smithsr{at}pbrc.edu)







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