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1Centre of Inflammation and Metabolism at Department of Infectious Diseases and 2Copenhagen Muscle Research Centre, Rigshospitalet, and 3Centre of Inflammation and Metabolism, Institute of Molecular Biology and Physiology, August Krogh Institute, University of Copenhagen, Copenhagen, Denmark
Submitted 28 May 2007 ; accepted in final form 6 August 2007
We hypothesized that the peroxisome proliferator-activated receptor-
coactivator-1 (PGC-1) family of transcriptional coactivators (PGC-1
, PGC-1β, and PRC) is differentially regulated by training once daily vs. training twice daily every second day and that this difference might be observed in the acute response to endurance exercise. Furthermore, we hypothesized that expression levels of the PGC-1 family differ with muscular fiber-type composition. Thus, before and after 10 wk of knee extensor endurance training, training one leg once daily and the other leg twice daily every second day, keeping the total amount of training for the legs equal, skeletal muscle mRNA expression levels of PGC-1
, PGC-1β, and PRC were determined in young healthy men (n = 7) in response to 3 h of acute exercise. No significant difference was found between the two legs, suggesting that regulation of the PGC-1 family is independent of training protocol. Training decreased PGC-1β in both legs, whereas PGC-1
was increased, but not significantly, in the leg training once daily. PRC did not change with training. Both PGC-1
and PRC were increased by acute exercise both before and after endurance training, whereas PGC-1β did not change. The mRNA levels of the PGC-1 family were examined in different types of human skeletal muscle (triceps, soleus, and vastus lateralis; n = 7). Only the expression level of PGC-1β differed and correlated inversely with percentage of type I fibers. In conclusion, there was no difference between training protocols on the acute exercise and training response of the PGC-1 family. However, training caused a decrease in PGC-1β mRNA levels.
peroxisome proliferator-activated receptor-
coactivator-1; peroxisome proliferator-activated receptor-
coactivator-1β; peroxisome proliferator-activated receptor-
coactivator-1-related cofactor; adaptation; glycogen
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