4.6 Article

Bioenergetic basis for the increased fatigability with ageing

Journal

JOURNAL OF PHYSIOLOGY-LONDON
Volume 597, Issue 19, Pages 4943-4957

Publisher

WILEY
DOI: 10.1113/JP277803

Keywords

ageing; muscle fatigue; 31P-MRS; inorganic phosphate; acidosis; diprotonated phosphate; metabolism

Funding

  1. NIA NIH HHS [R01 AG048262, F31 AG052313] Funding Source: Medline

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Key points The mechanisms for the age-related increase in fatigability during dynamic exercise remain elusive. We tested whether age-related impairments in muscle oxidative capacity would result in a greater accumulation of fatigue causing metabolites, inorganic phosphate (P-i), hydrogen (H+) and diprotonated phosphate (H2PO4-), in the muscle of old compared to young adults during a dynamic knee extension exercise. The age-related increase in fatigability (reduction in mechanical power) of the knee extensors was closely associated with a greater accumulation of metabolites within the working muscle but could not be explained by age-related differences in muscle oxidative capacity. These data suggest that the increased fatigability in old adults during dynamic exercise is primarily determined by age-related impairments in skeletal muscle bioenergetics that result in a greater accumulation of metabolites. The present study aimed to determine whether the increased fatigability in old adults during dynamic exercise is associated with age-related differences in skeletal muscle bioenergetics. Phosphorus nuclear magnetic resonance spectroscopy was used to quantify concentrations of high-energy phosphates and pH in the knee extensors of seven young (22.7 +/- 1.2 years; six women) and eight old adults (76.4 +/- 6.0 years; seven women). Muscle oxidative capacity was measured from the phosphocreatine (PCr) recovery kinetics following a 24 s maximal voluntary isometric contraction. The fatiguing exercise consisted of 120 maximal velocity contractions (one contraction per 2 s) against a load equivalent to 20% of the maximal voluntary isometric contraction. The PCr recovery kinetics did not differ between young and old adults (0.023 +/- 0.007 s(-1 )vs. 0.019 +/- 0.004 s(-1), respectively). Fatigability (reductions in mechanical power) of the knee extensors was similar to 1.8-fold greater with age and was accompanied by a greater decrease in pH (young = 6.73 +/- 0.09, old = 6.61 +/- 0.04) and increases in concentrations of inorganic phosphate, [P-i], (young = 22.7 +/- 4.8 mm, old = 32.3 +/- 3.6 mm) and diprotonated phosphate, [H2PO4-], (young = 11.7 +/- 3.6 mm, old = 18.6 +/- 2.1 mm) at the end of the exercise in old compared to young adults. The age-related increase in power loss during the fatiguing exercise was strongly associated with intracellular pH (r = -0.837), [P-i] (r = 0.917) and [H2PO4-] (r = 0.930) at the end of the exercise. These data suggest that the age-related increase in fatigability during dynamic exercise has a bioenergetic basis and is explained by an increased accumulation of metabolites within the muscle.

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