Rapid exercise-induced changes in PGC-1alpha mRNA and protein in human skeletal muscle

The mRNA of the nuclear coactivator peroxisome proliferator-activated receptor-gamma coactivator-1alpha (PGC-1alpha) increases during prolonged exercise and is influenced by carbohydrate availability. It is unknown if the increases in mRNA reflect the PGC-1alpha protein or if glycogen stores are an...

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Veröffentlicht in:Journal of applied physiology (1985) 2008-10, Vol.105 (4), p.1098-1105
Hauptverfasser: Mathai, Anila S, Bonen, Arend, Benton, Carley R, Robinson, D L, Graham, Terry E
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container_end_page 1105
container_issue 4
container_start_page 1098
container_title Journal of applied physiology (1985)
container_volume 105
creator Mathai, Anila S
Bonen, Arend
Benton, Carley R
Robinson, D L
Graham, Terry E
description The mRNA of the nuclear coactivator peroxisome proliferator-activated receptor-gamma coactivator-1alpha (PGC-1alpha) increases during prolonged exercise and is influenced by carbohydrate availability. It is unknown if the increases in mRNA reflect the PGC-1alpha protein or if glycogen stores are an important regulator. Seven male subjects [23 +/- 1.3 yr old, maximum oxygen uptake (Vo(2 max)) 48.4 +/- 0.8 ml.kg(-1).min(-1)] exercised to exhaustion ( approximately 2 h) at 65% Vo(2 max) followed by ingestion of either a high-carbohydrate (HC) or low-carbohydrate (LC) diet (7 or 2.9 g.kg(-1).day(-1), respectively) for 52 h of recovery. Glycogen remained depressed in LC (P < 0.05) while returning to resting levels by 24 h in HC. PGC-1alpha mRNA increased both at exhaustion (3-fold) and 2 h later (6.2-fold) (P < 0.05) but returned to rest levels by 24 h. PGC-1alpha protein increased (P < 0.05) 23% at exhaustion and remained elevated for at least 24 h (P < 0.05). While there was no direct treatment effect (HC vs. LC) for PGC-1alpha mRNA or protein, there was a linear relationship between the changes in glycogen and those in PGC-1alpha protein during exercise and recovery (r = -0.68, P < 0.05). In contrast, PGC-1beta did not increase with exercise but rather decreased (P < 0.05) below rest level at 24 and 52 h, and the decrease was greater (P < 0.05) in LC. PGC-1alpha protein content increased in prolonged exercise and remained upregulated for 24 h, but this could not have been predicted by the changes in mRNA. The beta-isoform declined rather than increasing, and this was greater when glycogen was not resynthesized to rest levels.
doi_str_mv 10.1152/japplphysiol.00847.2007
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It is unknown if the increases in mRNA reflect the PGC-1alpha protein or if glycogen stores are an important regulator. Seven male subjects [23 +/- 1.3 yr old, maximum oxygen uptake (Vo(2 max)) 48.4 +/- 0.8 ml.kg(-1).min(-1)] exercised to exhaustion ( approximately 2 h) at 65% Vo(2 max) followed by ingestion of either a high-carbohydrate (HC) or low-carbohydrate (LC) diet (7 or 2.9 g.kg(-1).day(-1), respectively) for 52 h of recovery. Glycogen remained depressed in LC (P < 0.05) while returning to resting levels by 24 h in HC. PGC-1alpha mRNA increased both at exhaustion (3-fold) and 2 h later (6.2-fold) (P < 0.05) but returned to rest levels by 24 h. PGC-1alpha protein increased (P < 0.05) 23% at exhaustion and remained elevated for at least 24 h (P < 0.05). 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source MEDLINE; American Physiological Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Adult
Blood Glucose - metabolism
Carrier Proteins - metabolism
Cross-Over Studies
Diet, Carbohydrate-Restricted
Dietary Carbohydrates - administration & dosage
Dietary Carbohydrates - metabolism
Exercise - physiology
Fatty Acids, Nonesterified - blood
Glycogen - metabolism
Heat-Shock Proteins - genetics
Heat-Shock Proteins - metabolism
Humans
Insulin - blood
Male
Muscle Contraction
Muscle, Skeletal - metabolism
Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
Recovery of Function
RNA, Messenger - metabolism
Time Factors
Transcription Factors - genetics
Transcription Factors - metabolism
title Rapid exercise-induced changes in PGC-1alpha mRNA and protein in human skeletal muscle
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