A spinal mechanism related to left–right symmetry reduces cutaneous reflex modulation independently of speed during split-belt locomotion

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Abstract

Task-and phase-dependent reflex modulation during locomotion is well established, but we do not know the signals driving this modulation. To determine whether signals related to left–right symmetry of the locomotor pattern modulate cutaneous reflexes, we stimulated the superficial peroneal nerve in five intact female cats and in four spinal-transected cats (spinal cats, two males and two females) during split-belt locomotion at different left–right speeds. We compared cutaneous reflexes evoked in three ipsilateral and two contralateral hindlimb muscles during split-belt locomotion with those evoked during tied-belt (equal left–right speeds) locomotion at matched speeds of the slow and fast limbs. Our results showed similar phase-dependent modulation of cutaneous reflexes during tied-belt and split-belt locomotion in intact and spinal cats. During tied-belt locomotion in intact cats, an increase in speed significantly increased reflex modulationfromminimumtomaximumvalues,whereas inspinal cats, we observeda significant decrease. However, inall muscles of intact and spinal cats, split-belt locomotion significantly reduced reflex modulation compared with tied-belt locomotion independently of which limb was stepping onthe slowor fast belt. Additionally, reflex modulationcorrelatedmore withspatial left–right symmetry, as opposedtoa temporal one, in intact and spinal cats. Our results indicate that signals related to left–right symmetry reduce cutaneous reflex modulation independently of speed via a spinal mechanism. We propose that asymmetric sensory feedback from the left and right legs alters the state of the spinal network, thereby reducing cutaneous reflexes to prevent inputs from destabilizing a potentially unstable pattern.

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Hurteau, M. F., & Frigon, A. (2018). A spinal mechanism related to left–right symmetry reduces cutaneous reflex modulation independently of speed during split-belt locomotion. Journal of Neuroscience, 38(48), 10314–10328. https://doi.org/10.1523/JNEUROSCI.1082-18.2018

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