Department of Medicine, Jaume I University, Castellon, Spain.
Department of Physical Education and Sport, University of Valencia, Valencia, Spain.
J Appl Physiol (1985). 2020 Oct 1;129(4):873-879. doi: 10.1152/japplphysiol.00570.2020. Epub 2020 Sep 3.
Telomere shortening, a well-known biomarker of aging, is a complex process influenced by several intrinsic and lifestyle factors. Although habitual exercise may promote telomere length maintenance, extreme endurance exercise has been also associated with increased oxidative stress-presumed to be the major cause of telomere shortening. Therefore, the pace of telomere shortening with age may also depend on antioxidant system efficiency, which is, in part, genetically determined. In this study, we aimed to evaluate the impact of ultra-endurance exercise and oxidative stress susceptibility (determined by the rs4880 polymorphism in the superoxide dismutase 2 () gene) on telomere length. Genomic DNA was obtained from 53 sedentary individuals (34 females, 19-67 yr) and 96 ultra-trail runners (31 females, 23-58 yr). Indeed, blood samples before and after finishing a 107-km-trail race were collected from 69 runners to measure c-reactive protein (CRP) levels and, thus, analyze whether acute inflammation response is modulated by the rs4880 polymorphism. Our results revealed that telomere length was better preserved in ultra-trail runners compared with controls, especially in elderly runners who have been regularly training for many years. Carrying the rs4880*A allele was significantly associated with having shorter telomeres, as well as with having increased CRP levels after the ultra-trail race. In conclusion, habitual ultra-endurance exercise had a beneficial effect on telomere length maintenance, especially at older ages. This study also suggested that the rs4880 polymorphism may also have an impact on acute and chronic oxidative-related damage (inflammatory response and telomere length) after an ultra-trail race. Habitual ultra-endurance exercise seems to promote telomere length maintenance, especially at older ages. In addition, the beneficial effect of ultra-endurance training on biological aging is higher in ultra-trail runners who have been engaged to ultra-endurance training during many years. Finally, and for the first time, this study shows that the rs4880 polymorphism has a significant impact on telomere length, as well as on acute inflammatory response to a 107-km trail race.
端粒缩短是衰老的一个众所周知的生物标志物,是一个受多种内在和生活方式因素影响的复杂过程。虽然习惯性运动可能促进端粒长度的维持,但极端耐力运动也与氧化应激增加有关,氧化应激被认为是端粒缩短的主要原因。因此,端粒随年龄缩短的速度也可能取决于抗氧化系统的效率,而抗氧化系统的效率部分是由基因决定的。在这项研究中,我们旨在评估超耐力运动和氧化应激易感性(由超氧化物歧化酶 2()基因中的 rs4880 多态性决定)对端粒长度的影响。从 53 名久坐不动的个体(34 名女性,19-67 岁)和 96 名超长距离跑步者(31 名女性,23-58 岁)中获得基因组 DNA。实际上,从 69 名跑步者中采集了比赛前后的血液样本,以测量 C 反应蛋白(CRP)水平,从而分析急性炎症反应是否受到 rs4880 多态性的调节。我们的结果表明,与对照组相比,超长距离跑步者的端粒长度保存更好,尤其是那些经常训练多年的老年跑步者。携带 rs4880*A 等位基因与端粒较短以及超长距离赛跑后 CRP 水平升高显著相关。总之,习惯性超耐力运动对端粒长度的维持有有益的影响,尤其是在年龄较大时。这项研究还表明,rs4880 多态性也可能对超长距离赛跑后的急性和慢性氧化相关损伤(炎症反应和端粒长度)产生影响。习惯性超耐力运动似乎促进端粒长度的维持,尤其是在年龄较大时。此外,在多年从事超耐力训练的超长距离跑步者中,超耐力训练对生物衰老的有益影响更高。最后,也是首次,本研究表明 rs4880 多态性对端粒长度以及对 107 公里越野赛的急性炎症反应有显著影响。