TY - JOUR
T1 - Effects of tonic muscle pain on fusimotor control of human muscle spindles during isometric ankle dorsiflexion
AU - Smith, Lyndon J.
AU - Macefield, Vaughan G.
AU - Birznieks, Ingvars
AU - Burton, Alexander R.
PY - 2019
Y1 - 2019
N2 - Studies on anaesthetised animals have revealed that nociceptors can excite fusimotor neurones and thereby change the sensitivity of muscle spindles to stretch; such nociceptive reflexes have been suggested to underlie the mechanisms that lead to chronic musculoskeletal pain syndromes. However, the validity of the "vicious cycle" hypothesis in humans has yielded contrasting results to that found in animals. Given that spindle firing rates are much lower in humans than in animals, it is possible that some of the discrepancies between human experimental data and those obtained in animals could be explained by differences in background fusimotor drive when the leg muscles are relaxed. We examined the effects of tonic muscle pain during voluntary contractions of the ankle dorsiflexors. Unitary recordings were obtained from 10 fusimotor-driven muscle spindle afferents (6 primary, 4 secondary) supplying the ankle dorsiflexors via a microelectrode inserted percutaneously into the common peroneal nerve. A series of one-minute weak contractions was performed at rest and during one hour of muscle pain induced by intramuscular infusion of 5% hypertonic saline into the tibialis anterior muscle. We did not observe any statistically significant increases in muscle spindle firing rates of six afferents followed during tonic muscle pain, though discharge variability increased slightly. Furthermore, a participant's capacity to maintain a constant level of force, while relying on proprioceptive feedback in the absence of visual feedback, was not compromised during pain. We conclude that nociceptive inputs from contracting muscle do not excite fusimotor neurones during voluntary isometric contractions in humans.
AB - Studies on anaesthetised animals have revealed that nociceptors can excite fusimotor neurones and thereby change the sensitivity of muscle spindles to stretch; such nociceptive reflexes have been suggested to underlie the mechanisms that lead to chronic musculoskeletal pain syndromes. However, the validity of the "vicious cycle" hypothesis in humans has yielded contrasting results to that found in animals. Given that spindle firing rates are much lower in humans than in animals, it is possible that some of the discrepancies between human experimental data and those obtained in animals could be explained by differences in background fusimotor drive when the leg muscles are relaxed. We examined the effects of tonic muscle pain during voluntary contractions of the ankle dorsiflexors. Unitary recordings were obtained from 10 fusimotor-driven muscle spindle afferents (6 primary, 4 secondary) supplying the ankle dorsiflexors via a microelectrode inserted percutaneously into the common peroneal nerve. A series of one-minute weak contractions was performed at rest and during one hour of muscle pain induced by intramuscular infusion of 5% hypertonic saline into the tibialis anterior muscle. We did not observe any statistically significant increases in muscle spindle firing rates of six afferents followed during tonic muscle pain, though discharge variability increased slightly. Furthermore, a participant's capacity to maintain a constant level of force, while relying on proprioceptive feedback in the absence of visual feedback, was not compromised during pain. We conclude that nociceptive inputs from contracting muscle do not excite fusimotor neurones during voluntary isometric contractions in humans.
KW - motor ability
KW - motor neurons
KW - muscle receptors
KW - myalgia
UR - http://handle.westernsydney.edu.au:8081/1959.7/uws:49646
U2 - 10.1152/jn.00862.2018
DO - 10.1152/jn.00862.2018
M3 - Article
SN - 0022-3077
VL - 121
SP - 1143
EP - 1149
JO - Journal of Neurophysiology
JF - Journal of Neurophysiology
IS - 4
ER -