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Effects of Aging and Lifelong Aerobic Exercise on Basal and Exercise-Induced Inflammation in Women
Journal of Applied Physiology ( IF 3.3 ) Pub Date : 2020-10-15 , DOI: 10.1152/japplphysiol.00655.2020
Kaleen M Lavin 1 , Ryan K Perkins 1 , Bozena Jemiolo 1 , Ulrika Raue 1 , Scott W Trappe 1 , Todd A Trappe 1
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Low muscle mass and frailty are especially prevalent in older women and may be accelerated by age-related inflammation. Habitual physical activity throughout the lifespan (lifelong exercise) may prevent muscle inflammation and associated pathologies, but this is unexplored in women. This investigation assessed basal and acute exercise-induced inflammation in three cohorts of women: young exercisers (YE, n=10, 25±1y, VO2max:44±2mL/kg/min, quadriceps size:59±2cm2), old healthy non-exercisers (OH, n=10, 75±1y, VO2max:18±1mL/kg/min, quadriceps size:40±1cm2), and lifelong aerobic exercisers with a 48±2y aerobic training history (LLE, n=7, 72±2y, VO2max:26±2mL/kg/min, quadriceps size:42±2cm2). Resting serum IL-6, TNF-α, CRP, and IGF-1 were measured. Vastus lateralis muscle biopsies were obtained at rest (basal) and 4h after an acute exercise challenge (3x10reps, 70%1RM) to assess gene expression of cytokines (IL-6, TNF-α, IL-1β, IL-10, IL-4, IL-1Ra, TGF-β), chemokines (IL-8, MCP-1), cyclooxygenase enzymes (COX-1, COX-2), prostaglandin E2 synthases (mPGES-1, cPGES) and receptors (EP3-4), and macrophage markers (CD16b, CD163), as well as basal macrophage abundance (CD68+ cells). The older cohorts (LLE+OH combined) demonstrated higher muscle IL-6 and COX-1 (P≤0.05) than YE, while LLE expressed lower muscle IL-1β (P≤0.05 vs. OH). Acute exercise increased muscle IL-6 expression in YE only, whereas the older cohorts combined had higher postexercise expression of IL-8 and TNF-α (P≤0.05 vs. YE). Only LLE had increased postexercise expression of muscle IL-1β and MCP-1 (P≤0.05 vs. preexercise). Thus, aging in women led to mild basal and exercise-induced inflammation that was unaffected by lifelong aerobic exercise, which may have implications for long-term function and adaptability.

中文翻译:

衰老和终身有氧运动对女性基础炎症和运动诱发炎症的影响

低肌肉质量和虚弱在老年女性中尤其普遍,并且可能因与年龄相关的炎症而加速。整个生命周期的习惯性体育活动(终身锻炼)可以预防肌肉炎症和相关疾病,但这在女性中尚未得到探索。该调查评估了三组女性的基础和急性运动诱发的炎症:年轻锻炼者(YE,n=10, 25±1y,VO 2 max:44±2mL/kg/min,股四头肌大小:59±2cm 2),老年健康非锻炼者(OH,n=10,75±1y,VO 2 max:18±1mL/kg/min,股四头肌大小:40±1cm 2),以及有 48±2 年有氧训练历史的终生有氧锻炼者( LLE, n=7, 72±2y, VO 2 max:26±2mL/kg/min, 股四头肌大小:42±2cm 2)。测量静息血清 IL-6、TNF-α、CRP 和 IGF-1。在休息(基础)和急性运动挑战(3x10reps,70%1RM)后 4 小时获取股外侧肌活检,以评估细胞因子(IL-6、TNF-α、IL-1β、IL-10、IL- 4、IL-1Ra、TGF-β)、趋化因子(IL-8、MCP-1)、环氧合酶(COX-1、COX-2)、前列腺素E 2合酶(mPGES-1、cPGES)和受体(EP3- 4) 和巨噬细胞标记物 (CD16b, CD163),以及基础巨噬细胞丰度 (CD68 +细胞)。较老的队列(LLE+OH 组合)表现出比 YE 更高的肌肉 IL-6 和 COX-1(P≤0.05),而 LLE 表达的肌肉 IL-1β 较低(P≤0.05 vs. OH)。急性运动仅在 YE 中增加肌肉 IL-6 表达,而年龄较大的队列结合起来具有更高的运动后 IL-8 和 TNF-α 表达(与 YE 相比 P≤0.05)。只有 LLE 增加了肌肉 IL-1β 和 MCP-1 的运动后表达(与运动前相比,P≤0.05)。因此,女性衰老导致轻度基础和运动诱发的炎症,而终身有氧运动不会影响这些炎症,这可能对长期功能和适应性产生影响。
更新日期:2020-10-16
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