Rota Viviana, Caronni Antonio, Scarano Stefano, Amadei Maurizio, Tesio Luigi
IRCCS Istituto Auxologico Italiano, Department of Neurorehabilitation Sciences, Ospedale San Luca, Milan, Italy.
Department of Biomedical Sciences for Health, Università Degli Studi di Milano, Milan, Italy.
Front Sports Act Living. 2025 Jul 8;7:1595065. doi: 10.3389/fspor.2025.1595065. eCollection 2025.
The plantar flexors contribute to the uniqueness of man's walking across bipeds (including apes). This role is achieved in late infancy through neural maturation. This may explain why this mechanism is lost with all corticospinal lesions despite the spared power of plantar flexors in segmental motions. During adult human walking, the plantar flexor muscles at the rear limb, during double stance, are suspected to provide most of the work and power required to translate the body system, which can be represented mechanically by its centre of mass (CoM). However, direct evidence of the dominant role of the ankle muscles in CoM translation is scarce. Experimental evidence requires synchronously assessing the lower limb joints' and CoM's power.
In this work, ten healthy adults were requested to walk on a split-belt force treadmill at speeds ranging from 0.3 to 1.2 m s. A series of eight subsequent strides was analysed at each different speed. The synchronous analysis of ground reaction forces (through force platforms) and joint rotations (through an optoelectronic system) allowed us to simultaneously measure the CoM and the lower limb joints' power.
The dominant role of the ankle plantar flexors, suggested by previous studies focusing on speeds above 0.9 m s, was confirmed by observing that changes in ankle power during the push-off phase (end of single stance and initial double stance) mirror the changes in power of the CoM. In the double support phase, the amplitude of the increments in ankle joint power was a strong predictor of the increments in CoM power ( = 82%).
Low walking speeds have been included to foster the interpretation of pathologic gaits, and clinical correlates of these findings in motor impairments are highlighted.
ClinicalTrials.gov, identifier NCT05778474.
跖屈肌有助于人类(包括猿类)两足行走的独特性。这一作用在婴儿晚期通过神经成熟得以实现。这或许可以解释为何尽管在节段性运动中跖屈肌力量尚存,但所有皮质脊髓损伤都会导致这种机制丧失。在成年人行走过程中,后肢的跖屈肌在双支撑期被认为提供了使身体系统平移所需的大部分功和功率,身体系统可通过其质心(CoM)进行力学表征。然而,关于踝关节肌肉在质心平移中起主导作用的直接证据却很稀少。实验证据需要同步评估下肢关节和质心的功率。
在本研究中,10名健康成年人被要求在分体式测力跑步机上以0.3至1.2米/秒的速度行走。在每个不同速度下分析随后的一系列8步。通过力平台同步分析地面反作用力以及通过光电系统同步分析关节旋转,使我们能够同时测量质心和下肢关节的功率。
先前针对速度高于0.9米/秒的研究表明踝关节跖屈肌起主导作用,本研究通过观察到蹬离期(单支撑末期和初始双支撑期)踝关节功率的变化反映了质心功率的变化,证实了这一点。在双支撑期,踝关节功率增量的幅度是质心功率增量的有力预测指标( = 82%)。
纳入低步行速度有助于对病理步态进行解读,并强调了这些发现与运动障碍临床相关性。
ClinicalTrials.gov,标识符NCT05778474。