Finger stability in precision grips

Abstract

Stable precision grips using the fingertips are a cornerstone of human hand dexterity. Occasionally, however, our fingers become unstable and snap into a hyper-extended posture. This is because multi-link mechanisms, like our fingers, can buckle under tip forces. Suppressing this instability is crucial for hand dexterity, but how the neuromuscular system does so is unknown. Here we show that finger stability is due to the stiffness from muscle contraction and likely not feedback control. We recorded maximal force application with the index finger and found that most buckling events lasted less than 50ms, too fast for sensorimotor feedback to act. However, a biomechanical model of the finger predicted that muscle-induced stiffness is also insufficient for stability at maximal force unless we add springs to stiffen the joints. We tested this prediction in 39 volunteers. Upon adding stiffness, maximal force increased by 34±3%, and muscle electromyography readings were 21±3% higher for the finger flexors (mean±standard error). Hence, people refrain from applying truly maximal force unless an external stabilizing stiffness allows their muscles to apply higher force without losing stability. Muscle recordings and mathematical modeling show that the splint offloads the demand for muscle co-contraction and this reduced co-contraction with the splint underlies the increase in force. But more stiffness is not always better. Stiff fingers would interfere the ability to passively adapt to complex object geometries and precisely regulate force. Thus, our results show how hand function arises from neurally tuned muscle stiffness that balances finger stability with compliance.