Literature DB >> 3783240

PAD and PAH response patterns of group Ia- and Ib-fibers to cutaneous and descending inputs in the cat spinal cord.

P Rudomin, M Solodkin, I Jiménez.   

Abstract

The characteristics of the primary afferent depolarization (PAD) of Ia- and Ib-fibers generated by segmental and descending inputs have been analyzed in the spinal cord of anesthetized cats. The PAD was inferred from the changes produced by conditioning inputs on the intraspinal stimulus current required to produce a constant antidromic firing of single group I afferent fibers from the gastrocnemius (GS) or posterior biceps and semitendinosus (PBSt) nerves. Group I GS and PBSt fibers ending in the intermediate nucleus could be classified in three different types according to their PAD patterns in response to stimulation of cutaneous nerves and of descending fibers. In one set of group I fibers stimulation of cutaneous nerves and of the ipsilateral brain stem reticular formation, or the contralateral red nucleus, produced no PAD, but was able to inhibit the PAD generated by stimulation of group I fibers from flexors (type A PAD pattern). PBSt nerve fibers with this PAD pattern had peripheral thresholds and conduction velocities between 1.01 and 1.56 times threshold and 76.3 to 118 m/s, respectively. A second set of group I fibers was found to be depolarized by cutaneous nerves as well as by stimulation of rubrospinal and reticulospinal fibers (type B PAD pattern). The peripheral thresholds and conduction velocities of PBSt afferent fibers with a type B PAD pattern were of 1.66-2.03 times threshold and 71-83 m/s, respectively. We found a third set of group I fibers that were also depolarized by reticulospinal and rubrospinal inputs, but not by cutaneous nerves that instead inhibited the PAD elicited by group I volleys in flexor nerves (type C PAD pattern). All PBSt afferent fibers with a type C PAD pattern, with the exception of two, had peripheral thresholds and velocities between 1.46 and 2.16 times threshold and between 72 and 89 m/s, respectively. Stimulation of the Deiter's nucleus was found to depolarize the intraspinal terminals of a small fraction of group I GS fibers with a type A PAD pattern and of all group I GS and PBSt fibers with type B and C PAD patterns. The PAD produced by vestibulospinal stimulation in fibers with type A and C PAD patterns could be inhibited by conditioning volleys applied to cutaneous nerves. It is suggested that group I afferent fibers from flexors and extensors with a type A PAD pattern are group Ia, and that most fibers with type B and type C PAD patterns are group Ib.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1986        PMID: 3783240     DOI: 10.1152/jn.1986.56.4.987

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


  31 in total

1.  Modulation of synaptic transmission from segmental afferents by spontaneous activity of dorsal horn spinal neurones in the cat.

Authors:  E Manjarrez; J G Rojas-Piloni; I Jimenez; P Rudomin
Journal:  J Physiol       Date:  2000-12-01       Impact factor: 5.182

2.  Tonic differential supraspinal modulation of PAD and PAH of segmental and ascending intraspinal collaterals of single group I muscle afferents in the cat spinal cord.

Authors:  P Rudomin; J Lomelí; J Quevedo
Journal:  Exp Brain Res       Date:  2004-06-30       Impact factor: 1.972

3.  Differential modulation of primary afferent depolarization of segmental and ascending intraspinal collaterals of single muscle afferents in the cat spinal cord.

Authors:  P Rudomin; J Lomelí; J Quevedo
Journal:  Exp Brain Res       Date:  2004-02-19       Impact factor: 1.972

4.  Bulbospinal inhibition of PAD elicited by stimulation of afferent and motor axons in the isolated frog spinal cord and brainstem.

Authors:  H González; I Jiménez; P Rudomin
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

5.  Effects of stimulation of group I afferents from flexor muscles on heterosynaptic facilitation of monosynaptic reflexes produced by Ia and descending inputs: a test for presynaptic inhibition.

Authors:  P Rudomin; I Jiménez; M Enriquez
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

6.  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

7.  Changes in PAD patterns of group I muscle afferents after a peripheral nerve crush.

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

8.  Reduction in thermal hyperalgesia by intrathecal administration of glycine and related compounds.

Authors:  R K Simpson; M Gondo; C S Robertson; J C Goodman
Journal:  Neurochem Res       Date:  1997-01       Impact factor: 3.996

9.  Nociception induces a differential presynaptic modulation of the synaptic efficacy of nociceptive and proprioceptive joint afferents.

Authors:  A Ramírez-Morales; E Hernández; P Rudomin
Journal:  Exp Brain Res       Date:  2021-06-08       Impact factor: 1.972

10.  Presynaptic control of transmission through group II muscle afferents in the midlumbar and sacral segments of the spinal cord is independent of corticospinal control.

Authors:  N C Aggelopoulos; S Chakrabarty; S A Edgley
Journal:  Exp Brain Res       Date:  2008-01-30       Impact factor: 1.972

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