Aubrey J Gray, Rebecca L Krupenevich, John A Batsis, Gregory S Sawicki, Jason R Franz
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Older adults averaged 44% lower k<sub>AT</sub> than younger adults at matched triceps surae activations during isokinetic dorsiflexion tasks on a dynamometer (p=0.046). Older adults also walked with a 17% higher net metabolic power (p=0.017) but indistinguishable peak Achilles tendon forces than younger adults. Thus, data implicate altered tendon length-tension relations with age more than differences in the operating region of those length-tension relations between younger and older adults. In addition, we discovered empirical evidence that lesser k<sub>AT</sub> - likely due to the shorter muscle lengths and thus higher relative activations it imposes - was positively correlated with higher net metabolic power during walking (r=-0.365, p=0.048). 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We recently proposed a theoretical premise by which age-related reductions in Achilles tendon stiffness (k<sub>AT</sub>) can disrupt the neuromechanics of calf muscle force production and contribute to faster rates of oxygen consumption during walking. The purpose of this study was to objectively evaluate this premise. We quantified k<sub>AT</sub> at a range of matched relative activations prescribed using electromyographic biofeedback and walking metabolic cost and ankle joint biomechanics in a group of 15 younger (age: 23±4 yrs) and 15 older adults (age: 72±5 yrs). Older adults averaged 44% lower k<sub>AT</sub> than younger adults at matched triceps surae activations during isokinetic dorsiflexion tasks on a dynamometer (p=0.046). Older adults also walked with a 17% higher net metabolic power (p=0.017) but indistinguishable peak Achilles tendon forces than younger adults. 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引用次数: 0
摘要
人们对老年人步行代谢成本增加的机制知之甚少。我们最近提出了一个理论前提,即与年龄有关的跟腱硬度(kAT)降低会破坏小腿肌肉发力的神经力学,并导致行走过程中耗氧量增加。本研究的目的是对这一假设进行客观评估。我们利用肌电生物反馈和步行代谢成本以及踝关节生物力学,对 15 名年轻人(年龄:23±4 岁)和 15 名老年人(年龄:72±5 岁)在一系列匹配的相对激活状态下的 kAT 进行了量化。在测力计上完成等速外展任务时,老年人在匹配的肱三头肌激活状态下的 kAT 平均比年轻人低 44%(p=0.046)。老年人行走时的净代谢功率也比年轻人高出 17%(p=0.017),但跟腱的峰值力却与年轻人无异。因此,这些数据表明,随着年龄的增长,肌腱的长度-张力关系发生了变化,而非年轻人和老年人之间这些长度-张力关系的作用区域存在差异。此外,我们还发现经验证据表明,较小的 kAT(可能是由于较短的肌肉长度,因此相对激活度较高)与行走时较高的净代谢功率呈正相关(r=-0.365,p=0.048)。这些结果为干预措施铺平了道路,干预措施的重点是恢复踝关节肌肉-肌腱单元的结构刚度,以改善老年人的行走能量。
Reduced Achilles tendon stiffness in aging associates with higher metabolic cost of walking.
The mechanisms responsible for increased metabolic cost of walking in older adults are poorly understood. We recently proposed a theoretical premise by which age-related reductions in Achilles tendon stiffness (kAT) can disrupt the neuromechanics of calf muscle force production and contribute to faster rates of oxygen consumption during walking. The purpose of this study was to objectively evaluate this premise. We quantified kAT at a range of matched relative activations prescribed using electromyographic biofeedback and walking metabolic cost and ankle joint biomechanics in a group of 15 younger (age: 23±4 yrs) and 15 older adults (age: 72±5 yrs). Older adults averaged 44% lower kAT than younger adults at matched triceps surae activations during isokinetic dorsiflexion tasks on a dynamometer (p=0.046). Older adults also walked with a 17% higher net metabolic power (p=0.017) but indistinguishable peak Achilles tendon forces than younger adults. Thus, data implicate altered tendon length-tension relations with age more than differences in the operating region of those length-tension relations between younger and older adults. In addition, we discovered empirical evidence that lesser kAT - likely due to the shorter muscle lengths and thus higher relative activations it imposes - was positively correlated with higher net metabolic power during walking (r=-0.365, p=0.048). These results pave the way for interventions focused on restoring ankle muscle-tendon unit structural stiffness to improve walking energetics in aging.
期刊介绍:
The Journal of Applied Physiology publishes the highest quality original research and reviews that examine novel adaptive and integrative physiological mechanisms in humans and animals that advance the field. The journal encourages the submission of manuscripts that examine the acute and adaptive responses of various organs, tissues, cells and/or molecular pathways to environmental, physiological and/or pathophysiological stressors. As an applied physiology journal, topics of interest are not limited to a particular organ system. The journal, therefore, considers a wide array of integrative and translational research topics examining the mechanisms involved in disease processes and mitigation strategies, as well as the promotion of health and well-being throughout the lifespan. Priority is given to manuscripts that provide mechanistic insight deemed to exert an impact on the field.