Document Detail


Fatty acids increase glucose uptake and metabolism in C2C12 myoblasts stably transfected with human lipoprotein lipase.
MedLine Citation:
PMID:  20628023     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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 C2C12 myoblasts. Control myoblasts or myoblasts stably transfected with human lipoprotein lipase (C2/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 C2/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 C2/LPL cells. Changes in glucose transport or hexokinase II did not explain the altered glucose disappearance in C2/LPL cells. Our results suggest that LPL overexpression in these cells leads to chronic metabolic adaptations that alter glucose uptake and retention.
Authors:
Warren H Capell; Isabel R Schlaepfer; Pamela Wolfe; Peter A Watson; Daniel H Bessesen; Michael J Pagliassotti; Robert H Eckel
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2010-07-13
Journal Detail:
Title:  American journal of physiology. Endocrinology and metabolism     Volume:  299     ISSN:  1522-1555     ISO Abbreviation:  Am. J. Physiol. Endocrinol. Metab.     Publication Date:  2010 Oct 
Date Detail:
Created Date:  2010-09-29     Completed Date:  2010-11-03     Revised Date:  2012-05-07    
Medline Journal Info:
Nlm Unique ID:  100901226     Medline TA:  Am J Physiol Endocrinol Metab     Country:  United States    
Other Details:
Languages:  eng     Pagination:  E576-83     Citation Subset:  IM    
Affiliation:
Division of Endocrinology, Metabolism, and Diabetes, University of Colorado at Denver and Health Sciences Center, Denver, Colorado, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Blotting, Western
Cell Line
Fat Emulsions, Intravenous / pharmacology*
Fatty Acids, Nonesterified / metabolism
Glucose / metabolism*
Humans
Lactones / pharmacology
Lipoprotein Lipase / antagonists & inhibitors,  genetics,  metabolism*
Lipoproteins / metabolism
Mice
Muscle, Skeletal / cytology,  enzymology,  metabolism*
Myoblasts / enzymology,  metabolism
Transfection
Triglycerides / metabolism
Grant Support
ID/Acronym/Agency:
DK-02935/DK/NIDDK NIH HHS; DK-26356/DK/NIDDK NIH HHS; DK-47416/DK/NIDDK NIH HHS; DK-69291/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/Fat Emulsions, Intravenous; 0/Fatty Acids, Nonesterified; 0/Lactones; 0/Lipoproteins; 0/Triglycerides; 0/lipoprotein triglyceride; 50-99-7/Glucose; 96829-58-2/orlistat; EC 3.1.1.34/Lipoprotein Lipase
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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