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Lifelong Endurance Exercise as a Countermeasure Against Age-Related (V) over dotO2max Decline: Physiological Overview and Insights from Masters Athletes

期刊

SPORTS MEDICINE
卷 50, 期 4, 页码 703-716

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ADIS INT LTD
DOI: 10.1007/s40279-019-01252-0

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资金

  1. University of Acala [FPI2016]
  2. Fondo de Investigaciones Sanitarias, Instituto de Salud Carlos III (FIS) [PI15/00558]
  3. Fondos FEDER

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Maximum oxygen consumption (VO2max) is not only an indicator of endurance performance, but also a strong predictor of cardiovascular disease and mortality. This physiological parameter is known to decrease with aging. In turn, physical exercise might attenuate the rate of aging-related decline in (V) over doyO(2max), which in light of the global population aging is of major clinical relevance, especially at advanced ages. In this narrative review, we summarize the evidence available from masters athletes about the role of lifelong endurance exercise on aging-related (V) over doyO(2max) decline, with examples of the highest VO2max values reported in the scientific literature for athletes across different ages (e.g., 35 ml.kg(-1)center dot min(-1) in a centenarian cyclist). These data suggest that a linear decrease in (V) over doyO(2max) might be possible if physical exercise loads are kept consistently high through the entire life span, with (V) over doyO(2max) values remaining higher than those of the general population across all ages. We also summarize the main physiological changes that occur with inactive aging at different system levels-pulmonary and cardiovascular function, blood O-2 carrying capacity, skeletal muscle capillary density and oxidative capacity-and negatively influence (V) over doyO(2max), and review how lifelong exercise can attenuate or even prevent most-but apparently not all (e.g., maximum heart rate decline)-of them. In summary, although aging seems to be invariably associated with a progressive decline in (V) over doyO(2max), maintaining high levels of physical exercise along the life span slows the multi-systemic deterioration that is commonly observed in inactive individuals, thereby attenuating age-related (V) over doyO(2max) decline.

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