Literature DB >> 7650612

Organization of neuronal systems mediating presynaptic inhibition of group II muscle afferents in the cat.

J S Riddell1, E Jankowska, J Huber.   

Abstract

1. The organization of neuronal systems mediating presynaptic control of transmission from group II muscle afferent fibres has been investigated by comparing the sources of presynaptic inhibition of fibres terminating in different segments of the spinal cord: fibres of the semitendinosus and lateral gastrocnemius muscle nerves terminating in the sacral segments and of the tibialis anterior and extensor digitorum longus muscle nerves terminating in the midlumbar segments. 2. Two measures of presynaptic inhibition were used: depolarization of the terminals of group II fibres (detected as changes in the excitability of single fibres to electrical stimuli) and a decrease in the effectiveness of their synaptic actions (detected as a decrease in the amplitude of monosynaptic field potentials evoked by group II muscle afferents). 3. Group II muscle afferents strongly depolarized all of the group II afferent fibres, while group I muscle afferents contributed to the depolarization of only a few. The majority of fibres were as effectively depolarized by cutaneous afferents as by the most effective muscle afferents. However, the effectiveness with which afferents of different nerves depolarized group II muscle afferent fibres in the sacral and midlumbar segments differed. The most effective afferents were those of nerves that provide the main input to dorsal horn interneurones in the same region of the spinal cord. The sources of depolarization of flexor and extensor fibres terminating in the same (sacral) segments were very similar. 4. The amplitudes of field potentials evoked by group II afferents were depressed by the same types of afferent as produced depolarization of group II afferent fibres. There was also a strong correlation between the effectiveness with which afferents of a given nerve induced depolarization of single fibres and depression of field potentials in the same segments. Since group II field potentials were depressed to a greater extent (by up to 90%) than group I field potentials (by no more than 20%) concurrently recorded in the intermediate zone of midlumbar segments, it appears that transmission from group II muscle afferents may be more strongly affected by presynaptic inhibition than that from group I muscle afferents. 5. The results suggest that the interneuronal systems responsible for the presynaptic control of transmission from group II muscle afferents have topographically restricted actions and an organization appropriate to a system of negative feedback control.

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Year:  1995        PMID: 7650612      PMCID: PMC1157855          DOI: 10.1113/jphysiol.1995.sp020596

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  30 in total

1.  Central inhibitory action attributable to presynaptic depolarization produced by muscle afferent volleys.

Authors:  J C ECCLES; R M ECCLES; F MAGNI
Journal:  J Physiol       Date:  1961-11       Impact factor: 5.182

2.  Excitability changes in afferent fibre terminations and their relation to slow potentials.

Authors:  P D WALL
Journal:  J Physiol       Date:  1958-06-18       Impact factor: 5.182

3.  Presynaptic inhibition of synaptic potentials evoked in cat spinal motoneurones by impulses in single group Ia axons.

Authors:  J D Clements; I D Forsythe; S J Redman
Journal:  J Physiol       Date:  1987-02       Impact factor: 5.182

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.  Field potentials generated by group II muscle afferents in the middle lumbar segments of the cat spinal cord.

Authors:  S A Edgley; E Jankowska
Journal:  J Physiol       Date:  1987-04       Impact factor: 5.182

6.  Properties of group I afferent fibres from semitendinosus muscle in the cat.

Authors:  C M Coppin; J J Jack; A K McIntyre
Journal:  J Physiol       Date:  1969-07       Impact factor: 5.182

7.  Primary afferent depolarization of myelinated fibres in the joint and interosseous nerves of the cat.

Authors:  E Jankowska; J S Riddell; D A McCrea
Journal:  J Physiol       Date:  1993-07       Impact factor: 5.182

8.  Ascending tract neurones processing information from group II muscle afferents in sacral segments of the feline spinal cord.

Authors:  J S Riddell; E Jankowska; I Hammar; Z Szabo-Läckberg
Journal:  J Physiol       Date:  1994-03-15       Impact factor: 5.182

9.  Reflex pathways from group II muscle afferents. 1. Distribution and linkage of reflex actions to alpha-motoneurones.

Authors:  A Lundberg; K Malmgren; E D Schomburg
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

10.  Closely coupled excitation of gamma-motoneurones by group III Muscle afferents with low mechanical threshold in the cat.

Authors:  P H Ellaway; P R Murphy; A Tripathi
Journal:  J Physiol       Date:  1982-10       Impact factor: 5.182

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  25 in total

1.  Field potentials generated by group II muscle afferents in the lower-lumbar segments of the feline spinal cord.

Authors:  J S Riddell; M Hadian
Journal:  J Physiol       Date:  2000-01-01       Impact factor: 5.182

Review 2.  Spinal interneuronal systems: identification, multifunctional character and reconfigurations in mammals.

Authors:  E Jankowska
Journal:  J Physiol       Date:  2001-05-15       Impact factor: 5.182

3.  On organization of a neuronal network in pathways from group II muscle afferents in feline lumbar spinal segments.

Authors:  E Jankowska; U Slawinska; I Hammar
Journal:  J Physiol       Date:  2002-07-01       Impact factor: 5.182

4.  Effects of leg muscle tendon vibration on group Ia and group II reflex responses to stance perturbation in humans.

Authors:  Marco Bove; Antonio Nardone; Marco Schieppati
Journal:  J Physiol       Date:  2003-05-30       Impact factor: 5.182

5.  Both dorsal horn and lamina VIII interneurones contribute to crossed reflexes from feline group II muscle afferents.

Authors:  S A Edgley; E Jankowska; P Krutki; I Hammar
Journal:  J Physiol       Date:  2003-09-08       Impact factor: 5.182

6.  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

7.  The actions of monoamines and distribution of noradrenergic and serotoninergic contacts on different subpopulations of commissural interneurons in the cat spinal cord.

Authors:  Ingela Hammar; B Anne Bannatyne; David J Maxwell; Stephen A Edgley; Elzbieta Jankowska
Journal:  Eur J Neurosci       Date:  2004-03       Impact factor: 3.386

8.  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

9.  Properties of axon terminals contacting intermediate zone excitatory and inhibitory premotor interneurons with monosynaptic input from group I and II muscle afferents.

Authors:  Ting Ting Liu; B Anne Bannatyne; Elzbieta Jankowska; David J Maxwell
Journal:  J Physiol       Date:  2010-09-13       Impact factor: 5.182

10.  Patterns of primary afferent depolarization of segmental and ascending intraspinal collaterals of single joint afferents in the cat.

Authors:  P Rudomin; J Lomelí
Journal:  Exp Brain Res       Date:  2006-08-01       Impact factor: 1.972

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