Increased Subsarcolemmal Lipids in Type 2 Diabetes: Effect of Training on Localization of Lipids, Mitochondria, and Glycogen in Sedentary Human Skeletal Muscle
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Physiology
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The purpose of the study was to investigate the effect of aerobic training and type 2 diabetes on intramyocellular localization of lipids, mitochondria, and glycogen. Obese type 2 diabetic patients (n = 12) and matched obese controls (n = 12) participated in aerobic cycling training for 10 wk. Endurance-trained athletes (n = 15) were included for comparison. Insulin action was determined by euglycemic-hyperinsulinemic clamp. Intramyocellular contents of lipids, mitochondria, and glycogen at different subcellular compartments were assessed by transmission electron microscopy in biopsies obtained from vastus lateralis muscle. Type 2 diabetic patients were more insulin resistant than obese controls and had threefold higher volume of subsarcolemmal (SS) lipids compared with obese controls and endurance-trained subjects. No difference was found in intermyofibrillar lipids. Importantly, following aerobic training, this excess SS lipid volume was lowered by approximately 50%, approaching the levels observed in the nondiabetic subjects. A strong inverse association between insulin sensitivity and SS lipid volume was found (r(2)=0.62, P = 0.002). The volume density and localization of mitochondria and glycogen were the same in type 2 diabetic patients and control subjects, and showed in parallel with improved insulin sensitivity a similar increase in response to training, however, with a more pronounced increase in SS mitochondria and SS glycogen than in other localizations. In conclusion, this study, estimating intramyocellular localization of lipids, mitochondria, and glycogen, indicates that type 2 diabetic patients may be exposed to increased levels of SS lipids. Thus consideration of cell compartmentation may advance the understanding of the role of lipids in muscle function and type 2 diabetes.
Wilburn D, Fletcher E, Papoutsi E, Bohannon W, Haynatzki G, Zechmann B EXCLI J. 2024; 23:1208-1225.
PMID: 39574966 PMC: 11579521. DOI: 10.17179/excli2024-7592.
Schleh M, Ryan B, Ahn C, Ludzki A, Van Pelt D, Pitchford L Acta Physiol (Oxf). 2024; 241(1):e14249.
PMID: 39487600 PMC: 11674998. DOI: 10.1111/apha.14249.
Parry H, Willingham T, Giordano K, Kim Y, Qazi S, Knutson J J Physiol. 2024; 602(9):1967-1986.
PMID: 38564214 PMC: 11068488. DOI: 10.1113/JP286246.
Schleh M, Ahn C, Ryan B, Chugh O, Luker A, Luker K Am J Physiol Endocrinol Metab. 2023; 325(5):E466-E479.
PMID: 37729021 PMC: 10864005. DOI: 10.1152/ajpendo.00093.2023.
Ispoglou T, Wilson O, McCullough D, Aldrich L, Ferentinos P, Lyall G Biology (Basel). 2023; 12(7).
PMID: 37508325 PMC: 10376679. DOI: 10.3390/biology12070892.