Key result
Habitual exercise linked to preventing the ~116% age-related increase in endothelial cell senescence markers.
Why the study?
Does habitual exercise prevent age-related endothelial cell senescence and vascular endothelial dysfunction in healthy adults?
Cross-Sectional
Does habitual exercise prevent age-related endothelial cell senescence and vascular endothelial dysfunction in healthy adults?
p-value: p=<0.05
Habitual aerobic exercise is associated with the prevention of age-related endothelial cell senescence and the preservation of vascular endothelial function in healthy older adults.
Supports exercise mitigating endothelial senescence; leaves open causality and clinical vascular outcomes in prospective studies.
Cellular senescence is emerging as a key mechanism of age-related vascular endothelial dysfunction, but evidence in healthy humans is lacking. Moreover, the influence of lifestyle factors such as habitual exercise on endothelial cell (EC) senescence is unknown. We tested the hypothesis that EC senescence increases with sedentary, but not physically active, aging and is associated with vascular endothelial dysfunction. Protein expression (quantitative immunofluorescence) of p53, a transcription factor related to increased cellular senescence, and the cyclin-dependent kinase inhibitors p21 and p16 were 116%, 119%, and 128% greater (all P < 0.05), respectively, in ECs obtained from antecubital veins of older sedentary (60 ± 1 yr, n = 12) versus young sedentary (22 ± 1 yr, n = 9) adults. These age-related differences were not present (all P > 0.05) in venous ECs from older exercising adults (57 ± 1 yr, n = 13). Furthermore, venous EC protein levels of p53 ( r = −0.49, P = 0.003), p21 ( r = −0.38, P = 0.03), and p16 ( r = −0.58, P = 0.002) were inversely associated with vascular endothelial function (brachial artery flow-mediated dilation). Similarly, protein expression of p53 and p21 was 26% and 23% higher (both P < 0.05), respectively, in ECs sampled from brachial arteries of healthy older sedentary (63 ± 1 yr, n = 18) versus young sedentary (25 ± 1 yr, n = 9) adults; age-related changes in arterial EC p53 and p21 expression were not observed ( P > 0.05) in older habitually exercising adults (59 ± 1 yr, n = 14). These data indicate that EC senescence is associated with sedentary aging and is linked to endothelial dysfunction. Moreover, these data suggest that prevention of EC senescence may be one mechanism by which aerobic exercise protects against endothelial dysfunction with age. NEW & NOTEWORTHY Our study provides novel evidence in humans of increased endothelial cell senescence with sedentary aging, which is associated with impaired vascular endothelial function. Furthermore, our data suggest an absence of age-related increases in endothelial cell senescence in older exercising adults, which is linked with preserved vascular endothelial function. Listen to this article's corresponding podcast at http://ajpheart.podbean.com/e/aging-exercise-and-endothelial-cell-senescence/ .
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Rossman et al. (2017) conducted a cross-sectional in Healthy humans. Habitual exercise vs. Sedentary lifestyle was evaluated on Endothelial cell senescence (protein expression of p53, p21, and p16) (p=<0.05). Habitual exercise in older adults prevented the 116-128% age-related increases in venous endothelial cell senescence markers (p53, p21, p16) seen in sedentary older adults (all P<0.05).
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