Distribution of oligosynaptic group I input to the cat medial gastrocnemius motoneuron pool
- 1 February 1985
- journal article
- research article
- Published by American Physiological Society in Journal of Neurophysiology
- Vol. 53 (2) , 497-517
- https://doi.org/10.1152/jn.1985.53.2.497
Abstract
To characterize the oligosynaptic group 1 afferent input to the cat medial gastrocnemius (MG) motoneuron pool, the medial branch of the tibial nerve (MTIB: flexor digitorum and hallucis longus, popliteus, tibialis posterior and interosseous nerves), the nerves to flexor digitorum and hallucis longus (FDHL), or the nerves to the quadriceps muscles (QUAD) were stimulated at submaximal group I strength while recording intracellularly from MG motoneurons. Since previous work indicates that stimulation of these nerves at group I strength produces no significant monosynaptic Ia excitation or Renshaw inhibition of MG motoneurons, group I effects were assumed to be predominantly, though not exclusively, due to the action of Ib-fibers. MTIB, FDHL and QUAD postsynaptic potentials (PSP) were most commonly inhibitory. Since the MTIB, FDHL and QUAD nerves are composed predominantly of fibers innervating muscles with extensor action, their inhibitory effect on MG motoneurons is consistent with previous findings that stimulation of Ib-afferents in nerves to extensor muscles produces di- and trisynaptic inhibition of extensor motoneurons. Excitatory effects were observed in .apprx. 1/3 of the motoneurons, indicating that oligosynaptic group I input is not homogeneously distributed within the MG motoneuron pool. Variations in QUAD, FDHL and MTIB PSP pattern and amplitude were correlated with variations in the PSP pattern evoked by stimulation of the sural nerve: excitatory oligosynaptic group I PSP generally appeared in motoneurons receiving excitatory cutaneous (sural nerve) input, whereas inhibitory PSP generally appeared in motoneurons receiving some inhibitory cutaneous input and were largest in motoneurons receiving predominantly inhibition from the sural nerve. These variations in QUAD, FDHL and MTIB PSP pattern and amplitude were not due to variations in resting potential and were only partly due to variations in intrinsic motoneuron properties or motoneuron type. Activation of these cutaneous and group I muscle afferents exerts similar effects on the MG motoneuron pool. The presence of a strong correlation betwen the distributions of cutaneous and oligosynaptic group I PSP within a single motoneuron pool is consistent with the results of previous studies that have shown that some of the input to motoneurons from these peripheral afferents is mediated through common interneurons.This publication has 28 references indexed in Scilit:
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