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对乙酰氨基酚和布洛芬对老年人抵抗运动引起的骨骼肌适应性的影响。

Influence of acetaminophen and ibuprofen on skeletal muscle adaptations to resistance exercise in older adults.

机构信息

Human Performance Laboratory, Ball State Univ., Muncie, IN 47306, USA.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2011 Mar;300(3):R655-62. doi: 10.1152/ajpregu.00611.2010. Epub 2010 Dec 15.

Abstract

Evidence suggests that consumption of over-the-counter cyclooxygenase (COX) inhibitors may interfere with the positive effects that resistance exercise training has on reversing sarcopenia in older adults. This study examined the influence of acetaminophen or ibuprofen consumption on muscle mass and strength during 12 wk of knee extensor progressive resistance exercise training in older adults. Thirty-six individuals were randomly assigned to one of three groups and consumed the COX-inhibiting drugs in double-blind placebo-controlled fashion: placebo (67 ± 2 yr; n = 12), acetaminophen (64 ± 1 yr; n = 11; 4 g/day), and ibuprofen (64 ± 1 yr; n = 13; 1.2 g/day). Compliance with the resistance training program (100%) and drug consumption (via digital video observation, 94%), and resistance training intensity were similar (P > 0.05) for all three groups. Drug consumption unexpectedly increased muscle volume (acetaminophen: 109 ± 14 cm(3), 12.5%; ibuprofen: 84 ± 10 cm(3), 10.9%) and muscle strength (acetaminophen: 19 ± 2 kg; ibuprofen: 19 ± 2 kg) to a greater extent (P < 0.05) than placebo (muscle volume: 69 ± 12 cm(3), 8.6%; muscle strength: 15 ± 2 kg), when controlling for initial muscle size and strength. Follow-up analysis of muscle biopsies taken from the vastus lateralis before and after training showed muscle protein content, muscle water content, and myosin heavy chain distribution were not influenced (P > 0.05) by drug consumption. Similarly, muscle content of the two known enzymes potentially targeted by the drugs, COX-1 and -2, was not influenced (P > 0.05) by drug consumption, although resistance training did result in a drug-independent increase in COX-1 (32 ± 8%; P < 0.05). Drug consumption did not influence the size of the nonresistance-trained hamstring muscles (P > 0.05). Over-the-counter doses of acetaminophen or ibuprofen, when consumed in combination with resistance training, do not inhibit and appear to enhance muscle hypertrophy and strength gains in older adults. The present findings coupled with previous short-term exercise studies provide convincing evidence that the COX pathway(s) are involved in the regulation of muscle protein turnover and muscle mass in humans.

摘要

有证据表明,非处方环氧化酶(COX)抑制剂的摄入可能会干扰抗阻运动训练对老年人肌肉减少症的积极影响。本研究探讨了在 12 周的膝关节伸肌渐进抗阻运动训练过程中,摄入对乙酰氨基酚或布洛芬对肌肉质量和力量的影响。36 名参与者被随机分配到三组中的一组,并以双盲安慰剂对照的方式摄入 COX 抑制剂药物:安慰剂(67 ± 2 岁;n = 12)、对乙酰氨基酚(64 ± 1 岁;n = 11;4 g/天)和布洛芬(64 ± 1 岁;n = 13;1.2 g/天)。所有三组的抗阻训练计划(100%)和药物消耗(通过数字视频观察,94%)以及抗阻训练强度均相似(P > 0.05)。药物消耗出人意料地增加了肌肉体积(对乙酰氨基酚:109 ± 14 cm³,12.5%;布洛芬:84 ± 10 cm³,10.9%)和肌肉力量(对乙酰氨基酚:19 ± 2 kg;布洛芬:19 ± 2 kg),比安慰剂(肌肉体积:69 ± 12 cm³,8.6%;肌肉力量:15 ± 2 kg)更为显著(P < 0.05),而控制初始肌肉大小和强度后。训练前后取自股外侧肌的肌肉活检的随访分析表明,药物消耗不影响肌肉蛋白含量、肌肉含水量和肌球蛋白重链分布(P > 0.05)。同样,两种已知的可能成为药物靶点的酶(COX-1 和 COX-2)的肌肉含量不受药物消耗的影响(P > 0.05),尽管抗阻训练确实导致 COX-1 独立增加(32 ± 8%;P < 0.05)。药物消耗不影响未经抗阻训练的腘绳肌肌肉大小(P > 0.05)。在与抗阻训练相结合时,非处方剂量的对乙酰氨基酚或布洛芬不会抑制,并且似乎会增强老年人的肌肉肥大和力量增益。目前的研究结果与之前的短期运动研究相结合,提供了令人信服的证据表明,COX 途径(s)参与了人类肌肉蛋白周转和肌肉质量的调节。

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