Cardiovascular and skeletal muscle health with lifelong exercise

The purpose of this study was to examine the effects of aerobic lifelong exercise (LLE) on maximum oxygen consumption ((V) over dotO(2max)) and skeletal muscle metabolic fitness in trained women (n = 7, 72 +/- 2 yr) and men (n = 21, 74 +/- 1 yr) and compare them to old, healthy nonexercisers (OH; women: n = 10, 75 +/- 1 yr; men: n = 10, 75 +/- 1 yr) and young exercisers (YE; women: n = 10, 25 +/- 1 yr; men: n = 10, 25 +/- 1 yr). LLE men were further subdivided based on intensity of lifelong exercise and competitive status into performance (LLE-P, n = 14) and fitness (LLE-F, n = 7). On average, LLE exercised 5 day/wk for 7 h/wk over the past 52 +/- 1 yr. Each subject performed a maximal cycle test to assess (V) over dotO(2max) and had a vastus lateralis muscle biopsy to examine capillarization and metabolic enzymes [ citrate synthase, beta-hydroxyacyl-CoA dehydrogenase (eta-HAD), and glycogen phosphorylase]. (V) over dotO(2max) had a hierarchical pattern (YE > LLE > OH, P < 0.05) for women (44 +/- 2 > 26 +/- 2 > 18 +/- 1 ml.kg(-1).min(-1)) and men (53 +/- 3 > 34 +/- 1 > 22 +/- 1 ml.kg(-1).min(-1)) and was greater (P < 0.05) in LLE-P (38 +/- 1 ml.kg(-1).min(-1)) than LLE-F (27 +/- 2 ml.kg(-1).min(-1)). LLE men regardless of intensity and women had similar capillarization and aerobic enzyme activity (citrate synthase and beta-HAD) as YE, which were 20%-90% greater (P < 0.05) than OH. In summary, these data show a substantial (V) over dotO(2max) benefit with LLE that tracked similarly between the sexes, with further enhancement in performance-trained men. For skeletal muscle, 50 +/- years of aerobic exercise fully preserved capillarization and aerobic enzymes, regardless of intensity. These data suggest that skeletal muscle metabolic fitness may be easier to maintain with lifelong aerobic exercise than more central aspects of the cardiovascular system. NEW & NOTEWORTHY Lifelong exercise (LLE) is a relatively new and evolving area of study with information especially limited in women and individuals with varying exercise intensity habits. These data show a substantial maximal oxygen consumption benefit with LLE that tracked similarly between the sexes. Our findings contribute to the very limited skeletal muscle biopsy data from LLE women (> 70 yr), and similar to men, revealed a preserved metabolic phenotype comparable to young exercisers.