Hilkens Luuk, Boerboom Marleen, van Schijndel Nick, Bons Judith, van Loon Luc J C, van Dijk Jan-Willem
School of Sport and Exercise, HAN University of Applied Sciences, Nijmegen, the Netherlands; Department of Human Biology, NUTRIM, Maastricht University Medical Centre+, Maastricht, the Netherlands.
School of Sport and Exercise, HAN University of Applied Sciences, Nijmegen, the Netherlands.
Bone. 2023 May;170:116705. doi: 10.1016/j.bone.2023.116705. Epub 2023 Feb 16.
We assessed whether collagen supplementation augments the effects of high-impact exercise on bone turnover and whether a higher exercise frequency results in a greater benefit for bone metabolism.
In this randomized, cross-over trial, 14 healthy males (age 24 ± 4 y, BMI 22.0 ± 2.1 kg/m) performed 5-min of high-impact exercise once (JUMP+PLA and JUMP+COL) or twice daily (JUMP2+COL2) during a 3-day intervention period, separated by a 10-day wash out period. One hour before every exercise bout participants ingested 20 g hydrolysed collagen (JUMP+COL and JUMP2+COL2) or a placebo control (JUMP+PLA). Blood markers of bone formation (P1NP) and resorption (CTXI) were assessed in the fasted state before the ingestion of the initial test drinks and 24, 48, and 72 h thereafter. In JUMP+PLA and JUMP+COL, additional blood samples were collected in the postprandial state at 1, 2, 3, 4, 5 and 13 h after ingestion of the test drink.
In the postprandial state, serum P1NP concentrations decreased marginally from 99 ± 37 to 93 ± 33 ng/mL in JUMP+COL, and from 97 ± 32 to 92 ± 31 ng/mL in JUMP+PLA, with P1NP levels having returned to baseline levels after 13 h (time-effect, P = 0.053). No differences in serum P1NP concentrations were observed between JUMP+PLA and JUMP+COL (time x treatment, P = 0.58). Serum CTX-I concentrations showed a ~ 50 % decline (time, P < 0.001) in the postprandial state in JUMP+COL (0.9 ± 0.3 to 0.4 ± 0.2 ng/mL) and JUMP+PLA (0.9 ± 0.3 to 0.4 ± 0.2 ng/mL), with no differences between treatments (time x treatment, P = 0.17). Fasted serum P1NP concentrations increased ~8 % by daily jumping exercise (time-effect, P < 0.01), with no differences between treatments (time x treatment, P = 0.71). Fasted serum CTX-I concentrations did not change over time (time-effect, P = 0.41) and did not differ between treatments (time x treatment, P = 0.58).
Five minutes of high-impact exercise performed daily stimulates bone formation during a 3-day intervention period. This was indicated by an increase in fasted serum P1NP concentrations, rather than an acute increase in post-exercise serum P1NP concentrations. Collagen supplementation or an increase in exercise frequency does not further increase serum P1NP concentrations. The bone resorption marker CTX-I was not affected by daily short-duration high-impact exercise with or without concurrent collagen supplementation.
我们评估了补充胶原蛋白是否能增强高强度运动对骨转换的影响,以及更高的运动频率是否会给骨代谢带来更大益处。
在这项随机交叉试验中,14名健康男性(年龄24±4岁,体重指数22.0±2.1kg/m²)在为期3天的干预期内,每天进行一次5分钟的高强度运动(JUMP+PLA和JUMP+COL)或每天进行两次(JUMP2+COL2),中间间隔10天的洗脱期。每次运动前1小时,参与者摄入20克水解胶原蛋白(JUMP+COL和JUMP2+COL2)或安慰剂对照(JUMP+PLA)。在摄入初始测试饮料前的空腹状态以及此后的24、48和72小时,评估骨形成(P1NP)和骨吸收(CTXI)的血液标志物。在JUMP+PLA和JUMP+COL组中,在摄入测试饮料后的餐后状态下,于1、2、3、4、5和13小时采集额外的血样。
在餐后状态下,JUMP+COL组血清P1NP浓度从99±37ng/mL略微降至93±33ng/mL,JUMP+PLA组从97±32ng/mL降至92±31ng/mL,13小时后P1NP水平恢复到基线水平(时间效应,P=0.053)。JUMP+PLA和JUMP+COL组之间血清P1NP浓度无差异(时间×处理,P=0.58)。JUMP+COL组和JUMP+PLA组餐后状态下血清CTX-I浓度均下降约50%(时间,P<0.001)(分别从0.9±0.3降至0.4±0.2ng/mL和从0.9±0.3降至0.4±0.2ng/mL),处理间无差异(时间×处理,P=0.17)。每日跳跃运动使空腹血清P1NP浓度增加约8%(时间效应,P<0.01),处理间无差异(时间×处理,P=0.71)。空腹血清CTX-I浓度随时间无变化(时间效应,P=0.41),处理间也无差异(时间×处理,P=0.58)。
在为期3天的干预期内,每天进行5分钟的高强度运动可刺激骨形成。这表现为空腹血清P1NP浓度升高,而非运动后血清P1NP浓度的急性升高。补充胶原蛋白或增加运动频率不会进一步提高血清P1NP浓度。无论是否同时补充胶原蛋白,每日短时间高强度运动均不影响骨吸收标志物CTX-I。