Fatty acids increase glucose uptake and metabolism in C^sub 2^C^sub 12^ myoblasts stably transfected with human lipoprotein lipase

Cellular effects of FFA might differ from those of lipoprotein triglyceride (TG)-derived fatty acids (TGFA). The aim of the current study was to examine the relationship between lipoprotein lipase (LPL) expression, TGFA, or FFA availability and glucose metabolism in the absence of insulin in ... myo...

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Veröffentlicht in:American journal of physiology: endocrinology and metabolism 2010-10, Vol.299 (4), p.E576
Hauptverfasser: Capell, Warren H, Schlaepfer, Isabel R, Wolfe, Pamela, Watson, Peter A, Bessesen, Daniel H, Pagliassotti, Michael J, Eckel, Robert H
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Sprache:eng
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Zusammenfassung:Cellular effects of FFA might differ from those of lipoprotein triglyceride (TG)-derived fatty acids (TGFA). The aim of the current study was to examine the relationship between lipoprotein lipase (LPL) expression, TGFA, or FFA availability and glucose metabolism in the absence of insulin in ... myoblasts. Control myoblasts or myoblasts stably transfected with human lipoprotein lipase (.../LPL; 15-fold greater LPL activity) were incubated for 12 h in fetal bovine serum-free medium in the absence or presence of Intralipid-20. Intracellular retention of labeled medium glucose was assessed in a subset of experiments. In the presence of Intralipid, medium glucose disappearance was increased in .../LPL cells but not in control cells. In both cell types, glucose label retention in cellular TG was increased in the presence of Intralipid; incubation with albumin-bound oleate produced similar results. In the presence of Intralipid, the LPL hydrolytic inhibitor tetrahydrolipstatin blocked excess glucose retention in cellular TG but did not significantly decrease glucose disappearance in .../LPL cells. Changes in glucose transport or hexokinase II did not explain the altered glucose disappearance in .../LPL cells. Our results suggest that LPL overexpression in these cells leads to chronic metabolic adaptations that alter glucose uptake and retention. (ProQuest: ... denotes formulae/symbols omitted.)
ISSN:0193-1849
1522-1555