How knee muscles and ground reaction forces shape knee buckling and ankle push-off in neuromuscular simulations of human walking
Abstract Ankle push-off is important for efficient, human-like walking, and many prosthetic devices mimic push-off using motors or elastic elements. The knee is extended throughout the stance phase and begins to buckle just before push-off, with timing being crucial. However, the exact mechanisms be...
Saved in:
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2025-01-01
|
Series: | Scientific Reports |
Subjects: | |
Online Access: | https://doi.org/10.1038/s41598-025-86147-z |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832594850953822208 |
---|---|
author | Alexandra Buchmann Bernadett Kiss Alexander Badri-Spröwitz Daniel Renjewski |
author_facet | Alexandra Buchmann Bernadett Kiss Alexander Badri-Spröwitz Daniel Renjewski |
author_sort | Alexandra Buchmann |
collection | DOAJ |
description | Abstract Ankle push-off is important for efficient, human-like walking, and many prosthetic devices mimic push-off using motors or elastic elements. The knee is extended throughout the stance phase and begins to buckle just before push-off, with timing being crucial. However, the exact mechanisms behind this buckling are still unclear. We use a predictive neuromuscular simulation to investigate whether active muscles are required for knee buckling and to what extent ground reaction forces (GRFs) drive it. In a systematic parameter search, we tested how long the knee muscles vastus (VAS), gastrocnemius (GAS), and hamstrings could be deactivated while maintaining a stable gait with impulsive push-off. VAS deactivation up to 35% of the gait cycle resulted in a dynamic gait with increased ankle peak power. GAS deactivation up to 20% of the gait cycle was detrimental to gait efficiency and showed reduced ankle peak power. At the start of knee buckling, the GRF vector is positioned near the knee joint’s neutral axis, assisting in knee flexion. However, this mechanism is likely not enough to drive knee flexion independently. Our findings contribute to the biomechanical understanding of ankle push-off, with applications in prosthetic and bipedal robotic design, and fundamental research on human gait mechanics. |
format | Article |
id | doaj-art-a883ead8d3864b71802c760ae3c2b8d0 |
institution | Kabale University |
issn | 2045-2322 |
language | English |
publishDate | 2025-01-01 |
publisher | Nature Portfolio |
record_format | Article |
series | Scientific Reports |
spelling | doaj-art-a883ead8d3864b71802c760ae3c2b8d02025-01-19T12:18:16ZengNature PortfolioScientific Reports2045-23222025-01-0115111410.1038/s41598-025-86147-zHow knee muscles and ground reaction forces shape knee buckling and ankle push-off in neuromuscular simulations of human walkingAlexandra Buchmann0Bernadett Kiss1Alexander Badri-Spröwitz2Daniel Renjewski3Chair of Applied Mechanics, Technical University of MunichDynamic Locomotion Group, Max-Plank-Institute for Intelligent SystemsDynamic Locomotion Group, Max-Plank-Institute for Intelligent SystemsChair of Applied Mechanics, Technical University of MunichAbstract Ankle push-off is important for efficient, human-like walking, and many prosthetic devices mimic push-off using motors or elastic elements. The knee is extended throughout the stance phase and begins to buckle just before push-off, with timing being crucial. However, the exact mechanisms behind this buckling are still unclear. We use a predictive neuromuscular simulation to investigate whether active muscles are required for knee buckling and to what extent ground reaction forces (GRFs) drive it. In a systematic parameter search, we tested how long the knee muscles vastus (VAS), gastrocnemius (GAS), and hamstrings could be deactivated while maintaining a stable gait with impulsive push-off. VAS deactivation up to 35% of the gait cycle resulted in a dynamic gait with increased ankle peak power. GAS deactivation up to 20% of the gait cycle was detrimental to gait efficiency and showed reduced ankle peak power. At the start of knee buckling, the GRF vector is positioned near the knee joint’s neutral axis, assisting in knee flexion. However, this mechanism is likely not enough to drive knee flexion independently. Our findings contribute to the biomechanical understanding of ankle push-off, with applications in prosthetic and bipedal robotic design, and fundamental research on human gait mechanics.https://doi.org/10.1038/s41598-025-86147-zAnkle push-offKneeGastrocnemiusHamstringsVastusPredictive neuromuscular simulation |
spellingShingle | Alexandra Buchmann Bernadett Kiss Alexander Badri-Spröwitz Daniel Renjewski How knee muscles and ground reaction forces shape knee buckling and ankle push-off in neuromuscular simulations of human walking Scientific Reports Ankle push-off Knee Gastrocnemius Hamstrings Vastus Predictive neuromuscular simulation |
title | How knee muscles and ground reaction forces shape knee buckling and ankle push-off in neuromuscular simulations of human walking |
title_full | How knee muscles and ground reaction forces shape knee buckling and ankle push-off in neuromuscular simulations of human walking |
title_fullStr | How knee muscles and ground reaction forces shape knee buckling and ankle push-off in neuromuscular simulations of human walking |
title_full_unstemmed | How knee muscles and ground reaction forces shape knee buckling and ankle push-off in neuromuscular simulations of human walking |
title_short | How knee muscles and ground reaction forces shape knee buckling and ankle push-off in neuromuscular simulations of human walking |
title_sort | how knee muscles and ground reaction forces shape knee buckling and ankle push off in neuromuscular simulations of human walking |
topic | Ankle push-off Knee Gastrocnemius Hamstrings Vastus Predictive neuromuscular simulation |
url | https://doi.org/10.1038/s41598-025-86147-z |
work_keys_str_mv | AT alexandrabuchmann howkneemusclesandgroundreactionforcesshapekneebucklingandanklepushoffinneuromuscularsimulationsofhumanwalking AT bernadettkiss howkneemusclesandgroundreactionforcesshapekneebucklingandanklepushoffinneuromuscularsimulationsofhumanwalking AT alexanderbadrisprowitz howkneemusclesandgroundreactionforcesshapekneebucklingandanklepushoffinneuromuscularsimulationsofhumanwalking AT danielrenjewski howkneemusclesandgroundreactionforcesshapekneebucklingandanklepushoffinneuromuscularsimulationsofhumanwalking |