Literature DB >> 993824

Excitability changes of terminal arborizations of single Ia and Ib afferent fibers produced by muscle and cutaneous conditioning volleys.

W D Willis, R Núnez, P Rudomín.   

Abstract

1. In cats anesthetized with sodium pentobarbital, recordings were made from dorsal root ganglion (DRG) cells having a peripheral process in the gastrocnemius-soleus (GS) nerve. The GS nerve was left in continuity with the muscle to allow identification of group Ia and Ib fibers by responses of the receptors to muscle stretch and contraction. The central processes of the DRG cells were activated antidromically by stimulation within the spinal cord so that changes in the excitability of the fibers could be examined following conditioning volleys in muscle and cutaneous nerves. 2. Recordings were made from 44 DRG cells. Of these, 15 were group Ia and 9 group Ib afferents of the GS nerve. 3. Of 15 Ia fibers, 12 were activated antidromically by stimulation in the motor nucleus, but no Ib fibers were discharged by such stimulation. Ib fibers could be antidromically activated by stimulation in the intermediate nucleus. 4. The central processes of the Ia DRG cells had slower conduction velocities than did the peripheral processes. 5. The thresholds to electrical stimulation of the peripheral processes of Ia and Ib fibers of the GS nerve showed considerable overlap. 6. All of the Ia DRG cells tested showed an increased excitability following conditioning volleys in the biceps-semitendinosus (BST) nerve. The increase in excitability was produced by the largest fibers of the BST nerve. 7. Stimulation of the sural (SU) or superficial peroneal (SP) cutaneous nerves also increased the excitability of some Ia fibers. However, other Ia fibers were unaffected, and in two cases the excitability was reduced. 8. The excitability of group Ib fibers was increased by conditioning volleys in the BST, SU, or SP nerves. 9. It is concluded that cutaneous volleys produce a mixture of primary afferent depolarization and primary afferent hyperpolarization in Ia fibers of anesthetized cats. Such converse actions probably cancel in excitability tests using population responses. 10. The excitability of single Ia fibers is not stationary in excitability presumably reflect slow alterations within the central nervous system, perhaps related to spontaneous alterations in the level of tonically maintained primary afferent depolarization.

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Year:  1976        PMID: 993824     DOI: 10.1152/jn.1976.39.6.1150

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  10 in total

1.  Segmental and supraspinal control of synaptic effectiveness of functionally identified muscle afferents in the cat.

Authors:  M Enríquez; I Jiménez; P Rudomin
Journal:  Exp Brain Res       Date:  1996       Impact factor: 1.972

2.  Membrane properties and conduction velocity in sensory neurones following central or peripheral axotomy.

Authors:  G Czéh; N Kudo; M Kuno
Journal:  J Physiol       Date:  1977-08       Impact factor: 5.182

3.  A pharmacological study of group I muscle afferent terminals and synaptic excitation in the intermediate nucleus and Clarke's column of the cat spinal cord.

Authors:  D R Curtis; B D Gynther; R Malik
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

4.  PAD patterns of physiologically identified afferent fibres from the medial gastrocnemius muscle.

Authors:  I Jiménez; P Rudomin; M Solodkin
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

5.  Excitability changes of ankle extensor group Ia and Ib fibers during fictive locomotion in the cat.

Authors:  S H Dueñas; P Rudomin
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

6.  Evidence for primary afferent depolarization of single tooth-pulp afferents in the cat.

Authors:  S J Lisney
Journal:  J Physiol       Date:  1979-03       Impact factor: 5.182

7.  The depolarization of feline ventral horn group Ia spinal afferent terminations by GABA.

Authors:  D R Curtis; D Lodge
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

8.  Microwave oven burn.

Authors:  H Fleck
Journal:  Bull N Y Acad Med       Date:  1983-04

9.  Network actions of pentobarbital in the rat mesopontine tegmentum on sensory inflow through the spinothalamic tract.

Authors:  Dhananjay R Namjoshi; Shelly A McErlane; Niwat Taepavarapruk; Peter J Soja
Journal:  J Neurophysiol       Date:  2009-05-20       Impact factor: 2.714

10.  Central nervous stimulation in neurological disease.

Authors:  L S Illis
Journal:  J R Soc Med       Date:  1983-11       Impact factor: 18.000

  10 in total

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