Literature DB >> 28978544

Intramuscular triglyceride synthesis: importance in muscle lipid partitioning in humans.

Bryan C Bergman1, Leigh Perreault1, Allison Strauss1, Samantha Bacon1, Anna Kerege1, Kathleen Harrison1, Joseph T Brozinick2, Devon M Hunerdosse1, Mary C Playdon1, William Holmes3, Hai Hoang Bui2, Phil Sanders2, Parker Siddall2, Tao Wei2, Melissa K Thomas2, Ming Shang Kuo2, Robert H Eckel1.   

Abstract

Intramuscular triglyceride (IMTG) concentration is elevated in insulin-resistant individuals and was once thought to promote insulin resistance. However, endurance-trained athletes have equivalent concentration of IMTG compared with individuals with type 2 diabetes, and have very low risk of diabetes, termed the "athlete's paradox." We now know that IMTG synthesis is positively related to insulin sensitivity, but the exact mechanisms for this are unclear. To understand the relationship between IMTG synthesis and insulin sensitivity, we measured IMTG synthesis in obese control subjects, endurance-trained athletes, and individuals with type 2 diabetes during rest, exercise, and recovery. IMTG synthesis rates were positively related to insulin sensitivity, cytosolic accumulation of DAG, and decreased accumulation of C18:0 ceramide and glucosylceramide. Greater rates of IMTG synthesis in athletes were not explained by alterations in FFA concentration, DGAT1 mRNA expression, or protein content. IMTG synthesis during exercise in Ob and T2D indicate utilization as a fuel despite unchanged content, whereas IMTG concentration decreased during exercise in athletes. mRNA expression for genes involved in lipid desaturation and IMTG synthesis were increased after exercise and recovery. Further, in a subset of individuals, exercise decreased cytosolic and membrane di-saturated DAG content, which may help explain insulin sensitization after acute exercise. These data suggest IMTG synthesis rates may influence insulin sensitivity by altering intracellular lipid localization, and decreasing specific ceramide species that promote insulin resistance.

Entities:  

Keywords:  IMCL; intramyocellular triglyceride; sphingolipid

Mesh:

Substances:

Year:  2017        PMID: 28978544      PMCID: PMC5866414          DOI: 10.1152/ajpendo.00142.2017

Source DB:  PubMed          Journal:  Am J Physiol Endocrinol Metab        ISSN: 0193-1849            Impact factor:   4.310


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