J Physiol Volume 584, Number 3, 1011-1017, November 1, 2007 DOI: 10.1113/jphysiol.2007.140673
SKELETAL MUSCLE AND EXERCISE |
Regulation of skeletal muscle PPAR
mRNA expression in twins
Emma Nilsson1,
Pernille Poulsen1,
Marketa Sjögren2,
Charlotte Ling2,
Martin Ridderstråle3,
Leif Groop2 and
Allan Vaag1
1 Steno Diabetes Center, Gentofte, Denmark
2 Department of Clinical Sciences, Diabetes and Endocrinology
3 Department of Clinical Sciences, Clinical Obesity, Malmö University Hospital, Lund University, Sweden
Peroxisome proliferator-activated receptors (PPARs) are nuclear receptors regulating the expression of genes involved in lipid and glucose metabolism in a complex and to some extent unknown manner. Our aim was to study the impact of different factors on PPAR
mRNA expression in human skeletal muscle on one side, and the impact of PPAR
mRNA expression on these factors, including glucose and lipid metabolism, aerobic capacity, fibre type composition and lipid profile, on the other side. PPAR
mRNA levels were quantified by real-time PCR in muscle biopsies from 176 young and elderly monozygotic and dizygotic twins. Young twins had significantly increased PPAR
mRNA levels compared with elderly twins. A 2 h hyperinsulinaemic euglycaemic clamp had no significant effect on PPAR
mRNA levels. Biometric models were calculated for basal PPAR
mRNA expression to estimate the degree of genetic versus environmental influence. In both young and elderly twins there was a substantial genetic component influencing basal PPAR
mRNA levels. In a regression model, the muscle PPAR
mRNA expression was correlated to birth weight, central adiposity and age. The level of PPAR
mRNA was also positively correlated with markers for oxidative muscle fibres. However, in this apparently healthy study population, we found no correlations between PPAR
mRNA expression and aerobic capacity, lipid profile or glucose and lipid metabolism. In conclusion, we provide evidence that mRNA expression of PPAR
in human skeletal muscle is under genetic control but also influenced by factors such as age, birth weight and central adiposity.
(Received 13 July 2007;
accepted after revision 11 September 2007;
first published online 13 September 2007)
Corresponding author E. Nilsson: Steno Diabetes Center, Niels Steensens Vej 1, DK-2820 Gentofte, Denmark. Email: emmn{at}steno.dk
Copyright © 2007 The Physiological Society.