Institute of Health and Biomedical Innovation and School of Exercise and Nutrition Sciences, Queensland University of Technology (QUT), Brisbane, Queensland, Australia.
Robotics and Autonomous Systems, Data61, The Commonwealth Scientific and Industrial Research Organisation (CSIRO), Brisbane, Queensland, Australia.
J Sports Sci Med. 2020 Aug 13;19(3):469-477. eCollection 2020 Sep.
Muscle damage and soreness associated with increased exercise training loads or unaccustomed activity can be debilitating and impact the quality of subsequent activity/performance. Current techniques to assess muscle soreness are either time consuming, invasive or subjective. Infrared thermography has been identified as a quick, non-invasive, portable and athlete friendly method of assessing skin temperature. This study assessed the capability of thermal infrared imaging to detect skin temperature changes that may accompany the inflammatory response associated with delayed onset muscular soreness (DOMS). Eight recreationally trained participants (age 25 ± 3 years, mass 74.9 ± 13.6 kg, training minutes 296 ± 175 min·wk) completed 6 sets of 25 maximal concentric/eccentric contractions of the right knee flexors/extensors on a dynamometer to induce muscle damage and DOMS. The left knee extensors acted as a non-exercise control. Neuromuscular performance, subjective pain assessment and infrared thermography were undertaken at baseline, 24 and 48 hr post the DOMS-inducing exercise protocol. Data were analysed using Bayesian hierarchical regression and Cohen's was also calculated. Maximal voluntary contraction torque was statistically lower at 24 hr ( = -0.70) and 48 hr ( = -0.52) compared to baseline, after the DOMS-inducing exercise protocol. These neuromuscular impairments coincided with statistically higher ratings of muscle soreness at 24 hr ( = 0.96) and 48 hr ( = 0.48). After adjusting for ambient temperature, anterior thigh skin temperature was statistically elevated at 24 hr, but not 48 hr, compared with baseline, in both the exercised and non-exercised leg. Thigh temperature was not different statistically between legs at these time points. Infrared imaging was able to detect elevations in skin temperature, at 24 hrs after the DOMS inducing exercise protocol, in both the exercised and non-exercised thigh. Elevations in the skin temperature of both thighs, potentially identifies a systemic inflammatory response occurring at 24 hr after the DOMS-inducing exercise protocol.
与增加运动训练负荷或不习惯的活动相关的肌肉损伤和酸痛可能会使人衰弱,并影响随后的活动/表现质量。目前评估肌肉酸痛的技术要么耗时,要么具有侵入性或主观性。红外热成像已被确定为一种快速、非侵入性、便携和适合运动员的评估皮肤温度的方法。本研究评估了热红外成像检测可能伴随延迟性肌肉酸痛 (DOMS) 相关炎症反应的皮肤温度变化的能力。8 名有经验的训练参与者(年龄 25 ± 3 岁,体重 74.9 ± 13.6 公斤,训练时间 296 ± 175 分钟·周)在测力计上完成了 6 组 25 次右膝屈肌/伸肌的最大向心/离心收缩,以引起肌肉损伤和 DOMS。左膝伸肌作为非运动对照。在 DOMS 诱导运动方案后 24 和 48 小时,进行神经肌肉性能、主观疼痛评估和红外热成像。数据使用贝叶斯层次回归进行分析,并计算了 Cohen's 。与基线相比,在 DOMS 诱导运动方案后 24 小时( = -0.70)和 48 小时( = -0.52),最大自主收缩扭矩明显降低。这些神经肌肉损伤与 24 小时( = 0.96)和 48 小时( = 0.48)肌肉酸痛的评分明显升高一致。在调整环境温度后,与基线相比,在 DOMS 诱导运动方案后 24 小时,运动和非运动腿的前大腿皮肤温度均升高,但在 48 小时后未升高。在这些时间点,双腿之间的大腿温度没有统计学差异。红外成像能够在 DOMS 诱导运动方案后 24 小时检测到运动和非运动大腿皮肤温度升高。在 DOMS 诱导运动方案后 24 小时,两大腿的皮肤温度升高可能表明发生了全身性炎症反应。