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PMID: 12540388 Published · ppublish English Clinical Trial Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

A short-term, high-fat diet up-regulates lipid metabolism and gene expression in human skeletal muscle.

The American journal of clinical nutrition ·Vol. 77 ·No. 2 ·2003-02-00 ·Pages 313-8

Cameron-Smith D, Burke LM, Angus DJ, Tunstall RJ, Cox GR, Bonen A, Hawley JA, Hargreaves M

Abstract

Dietary fatty acids may be important in regulating gene expression. However, little is known about the effect of changes in dietary fatty acids on gene regulation in human skeletal muscle. The objective was to determine the effect of altered dietary fat intake on the expression of genes encoding proteins necessary for fatty acid transport and beta-oxidation in skeletal muscle. Fourteen well-trained male cyclists and triathletes with a mean (+/- SE) age of 26.9 +/- 1.7 y, weight of 73.7 +/- 1.7 kg, and peak oxygen uptake of 67.0 +/- 1.3 mL x kg(-1) x min(-1) consumed either a high-fat diet (HFat: > 65% of energy as lipids) or an isoenergetic high-carbohydrate diet (HCho: 70-75% of energy as carbohydrate) for 5 d in a crossover design. On day 1 (baseline) and again after 5 d of dietary intervention, resting muscle and blood samples were taken. Muscle samples were analyzed for gene expression [fatty acid translocase (FAT/CD36), plasma membrane fatty acid binding protein (FABPpm), carnitine palmitoyltransferase I (CPT I), beta-hydroxyacyl-CoA dehydrogenase (beta-HAD), and uncoupling protein 3 (UCP3)] and concentrations of the proteins FAT/CD36 and FABPpm. The gene expression of FAT/CD36 and beta -HAD and the gene abundance of FAT/CD36 were greater after the HFat than after the HCho diet (P < 0.05). Messenger RNA expression of FABPpm, CPT I, and UCP-3 did not change significantly with either diet. A rapid and marked capacity for changes in dietary fatty acid availability to modulate the expression of mRNA-encoding proteins is necessary for fatty acid transport and oxidative metabolism. This finding is evidence of nutrient-gene interactions in human skeletal muscle.

MeSH Terms
3-Hydroxyacyl CoA Dehydrogenases/genetics,metabolism Adult Bicycling CD36 Antigens Carnitine O-Palmitoyltransferase/genetics,metabolism Carrier Proteins/genetics,metabolism Cross-Over Studies Dietary Carbohydrates/administration & dosage,pharmacology Dietary Fats/administration & dosage,pharmacology Exercise/physiology Fatty Acid-Binding Protein 7 Fatty Acid-Binding Proteins Fatty Acids/genetics,metabolism Gene Expression Regulation/physiology Humans Ion Channels Lipid Metabolism Lipids/genetics Male Membrane Glycoproteins/genetics,metabolism Mitochondrial Proteins Muscle, Skeletal/metabolism Neoplasm Proteins Organic Anion Transporters/genetics,metabolism Oxidation-Reduction RNA, Messenger/metabolism Tumor Suppressor Proteins Uncoupling Protein 3 Up-Regulation
Chemicals
CD36 Antigens Carrier Proteins Dietary Carbohydrates Dietary Fats FABP7 protein, human Fatty Acid-Binding Protein 7 Fatty Acid-Binding Proteins Fatty Acids Ion Channels Lipids Membrane Glycoproteins Mitochondrial Proteins Neoplasm Proteins Organic Anion Transporters RNA, Messenger Tumor Suppressor Proteins UCP3 protein, human Uncoupling Protein 3 3-Hydroxyacyl CoA Dehydrogenases Carnitine O-Palmitoyltransferase
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Cameron-Smith David
School of Health Sciences, Deakin University, Burwood, Victoria, Australia. davidcs@deakin.edu.au
Burke Louise M
Angus Damien J
Tunstall Rebecca J
Cox Gregory R
Bonen Arend
Hawley John A
Hargreaves Mark
Article Info
Journal
The American journal of clinical nutrition
Abbr.
Am J Clin Nutr
ISSN
0002-9165
Published
2003-02-00
Pages
313-8
Language
English
Region
United States
NLM ID
0376027
Subset
IM
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