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PMID: 11095470 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Expression of genes involved in lipid metabolism correlate with peroxisome proliferator-activated receptor gamma expression in human skeletal muscle.

The Journal of clinical endocrinology and metabolism ·Vol. 85 ·No. 11 ·2000-11-00 ·Pages 4293-7

Lapsys NM, Kriketos AD, Lim-Fraser M, Poynten AM, Lowy A, Furler SM, Chisholm DJ, Cooney GJ

Abstract

Peroxisome proliferator-activated receptor gamma (PPAR-gamma) activation in adipose tissue is known to regulate genes involved in adipocyte differentiation and lipid metabolism. However, the role of PPAR-gamma in muscle remains unclear. To examine the potential regulation of genes by PPAR-gamma in human skeletal muscle, we used semiquantitative RT-PCR to determine the expression of PPAR-gamma, lipoprotein lipase (LPL), muscle carnitine palmitoyl transferase-1 (mCPT1), fatty acid-binding protein (FABP), carnitine acylcarnitine transferase (CACT), and glucose transporter-4 (GLUT4) in freeze-dried muscle samples from 14 male subjects. These samples were dissected free of adipose and other tissue contamination, as confirmed by minimal or absent adipsin expression. Between individuals, the messenger ribonucleic acid concentration of PPAR-gamma varied up to 3-fold, whereas LPL varied up to 6.5-fold, mCPT1 13-fold, FABP 4-fold, CACT 4-fold, and GLUT4 up to 3-fold. The expression of LPL (r2 = 0.54; P = 0.003), mCPT1 (r2 = 0.42; P = 0.012), and FABP (r2 = 0.324; P = 0.034) all correlated significantly with PPAR-gamma expression in the same samples. No significant correlation was observed between the expression of CACT and PPAR-gamma or between GLUT4 and PPAR-gamma. These findings demonstrate a relationship between PPAR-gamma expression and the expression of other genes of lipid metabolism in muscle and support the hypothesis that PPAR-gamma activators such as the antidiabetic thiazolidinediones may regulate fatty acid metabolism in skeletal muscle as well as in adipose tissue.

MeSH Terms
Aged Blood Glucose/metabolism Carnitine Acyltransferases/genetics Carrier Proteins/genetics Complement Factor D Fatty Acid-Binding Protein 7 Fatty Acid-Binding Proteins Fatty Acids, Nonesterified/blood Gene Expression Regulation Glucose Transporter Type 4 Humans Insulin/blood Lipid Metabolism Lipoprotein Lipase/genetics Male Middle Aged Monosaccharide Transport Proteins/genetics Muscle Proteins Muscle, Skeletal/metabolism Neoplasm Proteins Receptors, Cytoplasmic and Nuclear/genetics,physiology Reference Values Regression Analysis Reverse Transcriptase Polymerase Chain Reaction Serine Endopeptidases/genetics Transcription Factors/genetics,physiology Triglycerides/blood Tumor Suppressor Proteins
Chemicals
Blood Glucose Carrier Proteins FABP4 protein, human FABP7 protein, human Fabp4 protein, mouse Fatty Acid-Binding Protein 7 Fatty Acid-Binding Proteins Fatty Acids, Nonesterified Glucose Transporter Type 4 Insulin Monosaccharide Transport Proteins Muscle Proteins Neoplasm Proteins Receptors, Cytoplasmic and Nuclear SLC2A4 protein, human Transcription Factors Triglycerides Tumor Suppressor Proteins Carnitine Acyltransferases Lipoprotein Lipase Serine Endopeptidases CFD protein, human Complement Factor D complement factor D, mouse
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Lapsys N M
Metabolism and Diabetes Research Group, The Garvan Institute of Medical Research, Sydney, New South Wales, Australia. n.lapsys@garvan.unsw.edu.au
Kriketos A D
Lim-Fraser M
Poynten A M
Lowy A
Furler S M
Chisholm D J
Cooney G J
Article Info
Journal
The Journal of clinical endocrinology and metabolism
Abbr.
J Clin Endocrinol Metab
ISSN
0021-972X
Published
2000-11-00
Pages
4293-7
Language
English
Region
United States
NLM ID
0375362
Subset
IM
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