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The Journal of Neurophysiology Vol. 86 No. 3 September 2001, pp. 1321-1332
Copyright ©2001 by the American Physiological Society
1University Centre for Neuroscience and 2Department of Physiology, University of Alberta, Edmonton, Alberta T6G 2S2, Canada
Lam, Tania and
Keir G. Pearson.
Proprioceptive Modulation of Hip Flexor Activity During the
Swing Phase of Locomotion in Decerebrate Cats. J. Neurophysiol. 86: 1321-1332, 2001. This study examined the
influence of proprioceptive input from hip flexor muscles on the
activity in hip flexors during the swing phase of walking in the
decerebrate cat. One hindlimb was partially denervated to remove
cutaneous input and afferent input from most other hindlimb muscles.
Perturbations to hip movement were applied either by 1)
manual resistance or assistance to swing or by 2) resistance
to hip flexion using a device that blocked hip flexion but allowed leg
extension. Electromyographic recordings were made from the iliopsoas
(IP), sartorius, and medial gastrocnemius muscles. When the hip was
manually assisted into flexion, there was a reduction in hip flexor
burst activity. Conversely, when hip flexion was manually resisted or
mechanically blocked during swing, the duration and amplitude of hip
flexor activity was increased. We also found some specificity in the
role of afferents from individual hip flexor muscles in the modulation
of flexor burst activity. If the IP muscle was detached from its
insertion, little change in the response to blocking flexion was
observed. Specific activation of IP afferent fibers by stretching the
muscle also did not greatly affect flexor activity. On the other hand,
if conduction in the sartorius nerves was blocked, there was a
diminished response to blocking hip flexion. The increase in duration
of the flexor bursts still occurred, but this increase was consistently
lower than that observed when the sartorius nerves were intact. From these results we propose that during swing, feedback from hip flexor
muscle afferents, particularly those from the sartorius muscles,
enhances flexor activity. In addition, if we delayed the onset of
flexor activity in the contralateral hindlimb, blocking hip flexion
often resulted in the prolongation of ipsilateral flexor activity for
long periods of time, further revealing the reinforcing effects of
flexor afferent feedback on flexor activity. This effect was not seen
if conduction in the sartorius nerves was blocked. In conclusion, we
have found that hip flexor activity during locomotion can be strongly
modulated by modifying proprioceptive feedback from the hip flexor muscles.
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