Force Encoding in Muscle Spindles during Stretch of Passive Muscle


Meeting Abstract

P2-166  Friday, Jan. 5 15:30 – 17:30  Force Encoding in Muscle Spindles during Stretch of Passive Muscle BLUM, KP; LAMOTTE D’INCAMPS, B; ZYTNICKI, D; TING, LH*; Emory / Georgia Tech; Université Paris Descartes; Université Paris Descartes; Emory / Georgia Tech lting@emory.edu http://neuromechanicslab.emory.edu

Muscle spindle proprioceptive receptors play a primary role in encoding the effects of external mechanical perturbations to the body. During externally-imposed stretches of passive muscles, instantaneous firing rates (IFRs) of muscle spindles are associated with stretch length and velocity. However, there are history-dependent transients of muscle spindle firing that are not uniquely related to muscle length and velocity, nor reproduced by current muscle spindle models. These include acceleration-dependent initial bursts, increased dynamic response to stretch velocity if a muscle has been isometric, and rate relaxation, i.e., a decrease in tonic IFR when a muscle is held at a constant length after being stretched. We collected muscle spindle spike trains across a variety of muscle stretch kinematics, systematically altering stretch length, velocity, and acceleration. We show that muscle spindle primary afferents in passive muscle fire in direct relationship to muscle force-related variables, rather than length-related variables. Linear combinations of whole muscle-tendon force and the first time derivative of force (dF/dt) predict the entire time course of transient, history-dependent muscle spindle IFRs during muscle lengthening in passive muscle. Similar to acceleration scaling found previously in sensorimotor postural responses to perturbations, initial burst amplitude scaled equally well to initial stretch acceleration or dF/dt, though, later transients were only described by dF/dt. The transient increase in dF/dt at the onset of lengthening reflects muscle short-range stiffness due to cross-bridge dynamics, which play a critical role in history-dependent muscle spindle IFRs in passive muscle lengthening conditions relevant to the detection and sensorimotor response to mechanical perturbations to the body.

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