Literature DB >> 403249

Spinal cord potentials evoked by cutaneous afferents in the monkey.

J E Beall, A E Applebaum, R D Foreman, W D Willis.   

Abstract

1. Negative intermediary cord potentials and the equivalent field potentials were recorded from the surface or within the monkey lumbosacral spinal cord in response to stimulation of myelinated afferent fibers in cutaneous or mixed nerves of the hindlimb. 2. Cord potentials resembling the N1 and N2 potentials described in the cat spinal cord were found but, in addition, activation of small myelinated fibers produced a later potential named here the N3-wave. By use of a subtraction technique, it is estimated that the N3-wave has a latency of 11.4 (+/- 3.5 SD) ms from the time of arrival of the volley in the largest affs at 9 (+/- 3) ms after its onset, and the wave lasts 23 (+/- 5.7) ms. 3. The N3-wave is not lost following spinal cord transection, but may instead be enhanced. It is thus due to neural circuitry intrinsic to the lumbosacral spinal cord. 4. The longitudinal distribution of the N3-wave is similar to that of the N1- and N2-waves. 5. The field potential associated with the N3-wave and recorded from within the spinal cord has two negative foci in some animals: near the dorsalmost part of the dorsal horn and in an area equivalent to Rexed's laminae IV-VI. The field potential reverses in sign in the ventral horn. 6. The N3-wave is evoked by Adelta fibers. This was shown by grading the stimulus strength, by measuring the conduction delay for producing the wave when stimuli are applied either proximally or distally on the sural nerve, and by showing that the N3-wave persists when the Aalphabeta fibers are anodally blocked. 7. There is often a late burst discharge in spinal neurons, including spinothalamic tract neurons, which can be attributed to Adelta fibers and which corresponds in time to the N3-wave. 8. It is proposed that the N3-wave can be used as a monitor of the central effects of Adelta fibers in the spinal cord.

Entities:  

Mesh:

Year:  1977        PMID: 403249     DOI: 10.1152/jn.1977.40.2.199

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


  13 in total

1.  Field potentials and excitation of primate spinothalamic neurones in response to volleys in muscle afferents.

Authors:  R D Foreman; D R Kenshalo; R F Schmidt; W D Willis
Journal:  J Physiol       Date:  1979-01       Impact factor: 5.182

2.  Skin and epidural recording of spinal somatosensory evoked potentials following median nerve stimulation: correlation between the absence of spinal N13 and impaired pain sense.

Authors:  E Urasaki; S I Wada; C Kadoya; T Tokimura; A Yokota; S Matsuoka; A Fukumura; S Hamada
Journal:  J Neurol       Date:  1990-11       Impact factor: 4.849

3.  Responses of spinothalamic tract cells in the superficial dorsal horn of the primate lumbar spinal cord.

Authors:  D G Ferrington; L S Sorkin; W D Willis
Journal:  J Physiol       Date:  1987-07       Impact factor: 5.182

4.  Responses of spinal cord neurones to stimulation of articular afferent fibres in the cat.

Authors:  H G Schaible; R F Schmidt; W D Willis
Journal:  J Physiol       Date:  1986-03       Impact factor: 5.182

5.  Multivariate analysis of somatosensory evoked potential parameters in normal adults.

Authors:  H Strenge; A Gundel
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1983

6.  [Spinal and subcortical somatosensory evoked potentials after stimulation of the tibial nerve].

Authors:  B Riffel; M Stöhr
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1982

7.  Functional and topographical properties of field potentials evoked in rat dorsal horn by cutaneous C-fibre stimulation.

Authors:  J Schouenborg
Journal:  J Physiol       Date:  1984-11       Impact factor: 5.182

8.  Projection of a cutaneous nerve to the spinal cord of the pigeon. I. Evoked field potentials.

Authors:  R Necker
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

9.  Subcomponents of the cervical evoked response in patients with intracerebral circulatory arrest.

Authors:  T Ganes; P Nakstad
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-03       Impact factor: 10.154

10.  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

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