Department of Medicine, Division of Geriatric Medicine, University of Colorado Denver, Denver, CO 80045, USA.
J Bone Miner Res. 2010 Jun;25(6):1415-22. doi: 10.1002/jbmr.24.
Prostaglandins (PGs) are essential signaling factors in bone mechanotransduction. In animals, inhibition of the enzyme responsible for PG synthesis (cyclooxygenase) by nonsteroidal anti-inflammatory drugs (NSAIDs) blocks the bone-formation response to loading when administered before, but not immediately after, loading. The aim of this proof-of-concept study was to determine whether the timing of NSAID use influences bone mineral density (BMD) adaptations to exercise in humans. Healthy premenopausal women (n = 73) aged 21 to 40 years completed a supervised 9-month weight-bearing exercise training program. They were randomized to take (1) ibuprofen (400 mg) before exercise, placebo after (IBUP/PLAC), (2) placebo before, ibuprofen after (PLAC/IBUP), or (3) placebo before and after (PLAC/PLAC) exercise. Relative changes in hip and lumbar spine BMD from before to after exercise training were assessed using a Hologic Delphi-W dual-energy X-ray absorptiometry (DXA) instrument. Because this was the first study to evaluate whether ibuprofen use affects skeletal adaptations to exercise, only women who were compliant with exercise were included in the primary analyses (IBUP/PLAC, n = 17; PLAC/PLAC, n = 23; and PLAC/IBUP, n = 14). There was a significant effect of drug treatment, adjusted for baseline BMD, on the BMD response to exercise for regions of the hip (total, p < .001; neck, p = .026; trochanter, p = .040; shaft, p = .019) but not the spine (p = .242). The largest increases in BMD occurred in the group that took ibuprofen after exercise. Total-hip BMD changes averaged -0.2% +/- 1.3%, 0.4% +/- 1.8%, and 2.1% +/- 1.7% in the IBUP/PLAC, PLAC/PLAC, and PLAC/IBUP groups, respectively. This preliminary study suggests that taking NSAIDs after exercise enhances the adaptive response of BMD to exercise, whereas taking NSAIDs before may impair the adaptive response.
前列腺素 (PGs) 是骨骼机械转导中必不可少的信号因子。在动物中,通过非甾体抗炎药 (NSAIDs) 抑制负责 PG 合成的酶(环氧化酶),在负荷前但不在负荷后立即给药时,可阻止骨形成对负荷的反应。本概念验证研究的目的是确定 NSAID 的使用时间是否会影响人类运动对骨密度 (BMD) 的适应。73 名年龄在 21 至 40 岁的健康绝经前女性完成了为期 9 个月的监督负重运动训练计划。她们被随机分为三组:(1)运动前服用布洛芬(400mg),运动后服用安慰剂(IBUP/PLAC);(2)运动前服用安慰剂,运动后服用布洛芬(PLAC/IBUP);(3)运动前后均服用安慰剂(PLAC/PLAC)。使用 Hologic Delphi-W 双能 X 射线吸收仪 (DXA) 仪器评估运动训练前后髋部和腰椎 BMD 的相对变化。由于这是第一项评估布洛芬使用是否影响骨骼对运动的适应的研究,仅纳入了遵守运动计划的女性进行主要分析(IBUP/PLAC 组,n=17;PLAC/PLAC 组,n=23;PLAC/IBUP 组,n=14)。药物治疗对 BMD 对运动的反应有显著影响,调整了基线 BMD,影响了髋部区域的 BMD(总髋部,p<0.001;股骨颈,p=0.026;转子间区,p=0.040;骨干,p=0.019),但对脊柱无影响(p=0.242)。在运动后服用布洛芬的组中,BMD 增加最大。IBUP/PLAC、PLAC/PLAC 和 PLAC/IBUP 组的总髋部 BMD 变化平均值分别为-0.2%±1.3%、0.4%±1.8%和 2.1%±1.7%。这项初步研究表明,运动后服用 NSAIDs 可增强 BMD 对运动的适应性反应,而运动前服用 NSAIDs 可能会损害适应性反应。