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Effects of old age on human skeletal muscle energetics during fatiguing contractions with and without blood flow
Author(s) -
Lanza Ian R.,
Larsen Ryan G.,
KentBraun Jane A.
Publication year - 2007
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2007.138362
Subject(s) - energetics , skeletal muscle , blood flow , muscle contraction , human muscle , anatomy , medicine , chemistry , biology , ecology
We recently reported lower glycolytic flux (ATP GLY ) and increased reliance on oxidative ATP synthesis (ATP OX ) in contracting muscle of older compared to young humans. To further investigate this age‐related difference in the pathways of ATP synthesis, we used magnetic resonance spectroscopy to determine the rates of ATP OX , ATP GLY and net phosphocreatine hydrolysis in vivo during maximal muscle contractions under free‐flow (FF) and ischaemic (ISC) conditions in the ankle dorsiflexors of 20 young (27 ± 3 years; 10 male, 10 female) and 18 older (70 ± 5 years; 10 male, 8 female) adults. We hypothesized that ATP GLY would be higher in young compared to old during FF contractions, but that old would be unable to increase ATP GLY during ISC to match that of the young, which would suggest impaired glycolytic ATP synthesis with old age. Peak glycolytic flux during FF was lower in older (0.8 ± 0.1 m m ATP s −1 ) compared to young (1.4 ± 0.1 m m ATP s −1 , P < 0.001) subjects. During ISC, peak ATP GLY increased in old to a level similar to that of young (1.4 ± 0.2 m m ATP s −1 , 1.3 ± 0.2 m m ATP s −1 , respectively; P = 0.86), suggesting that glycolytic function remains intact in aged muscle in vivo . Notably, older adults fatigued less than young during both FF and ISC ( P ≤ 0.004). These results provide novel evidence of unimpaired in vivo glycolytic function in the skeletal muscle of older adults during maximal isometric dorsiflexion, and suggest a potential role for differences in metabolic economy and as a result, metabolite accumulation, in the fatigue resistance of the old.