Abstract
The bottom traces of Fig. 4.1A show the specimen records from the posterior epidural space (PES) of the lumbar enlargement in response to median nerve stimulation at the wrist in a wakeful subject. Any potentials were hardly noticeable in the lumbar enlargement. Thus, peripheral nerve stimulation at a distal site in the upper extremity can hardly evoke any potential change in the caudal segments of the spinal cord in a normal human. This, however, does not mean that peripheral nerve stimulation at a distal site in the upper extremity can hardly evoke any potential change in the caudal segments of the upper extremity or has no influence on spinal function in the lumbar enlargement. It is rather more likely that the electrical activity does exist but is barely demonstrated due to the temporal and spatial dispersion of the potential when the distal site of a peripheral nerve is stimulated. Therefore, it is predicted that when a more rostral site on the peripheral nerve is stimulated, a potential deflection could be more clearly demonstrated in the lumbosacral enlargement in humans, similar to that observed in the rat (Shimoji et al., 1986a,b,c).
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Section B: Chapter 4
Andersen P, Eccles JC, Sears TA. Presynaptic inhibitory action of cerebral cortex on the spinal cord. Nature 1962;194:740–1.
Basbaum AI, Ralston DD, Ralston HJ III. Bulbospinal projections in the primate: a light and electron microscopic study of a pain modulating system. J Comp Neurol 1986;250:311–23.
Besson JM, Rivot JP. Heterosegmental, heterosensory and cortical inhibitory effects on dorsal interneurones in the cat’s spinal cord. Electroencephalogr Clin Neurophysiol 1972;33:195–206.
Besson JM, Guilbaud G, Le Bars D. Descending inhibitory influences exerted by the brain stem upon the activities of dorsal horn lamina V cells induced by intra-arterial injection of bradykinin into the limb. J Physiol (Lond) 1975;248:725–39.
Carpenter D, Engberg I, Lundberg A. Primary afferent depolarization evoked from the brain stem and the cerebellum. Arch Ital Biol 1966;104:73–85.
Denda S, Shimoji K, Tomita M, Baba H, Yamakura T, Masaki H, Endoh H, Fukuda, S. Central nuclei and spinal pathways in feedback inhibitory spinal cord potentials in ketamineanaesthetized rats. Br J Anaesth 1996;76:258–65.
Fung SJ, Barnes CD. Locus coeruleus control of spinal cord activity. In: Barnes CD, editor. Brainstem control of spinal cord function. Orlando: Academic Press; 1984. p. 215–55.
Gebhart GF. Descending modulation of pain (Review). Neurosci Biobehav Rev 2004;27:729–37.
Mokha SS, McMillan JA, Iggo A. Pathways mediating descending control of spinal nociceptive transmission from the nuclei locus coeruleus (LC) and raphe magnus (NRM) in the cat. Exp Brain Res 1986;61:597–606.
Morton CR, Maisch B, Zimmermann M. Diffuse noxious inhibitory controls of lumbar spinal neurons involve a supraspinal loop in the cat. Brain Res 1987;410:347–52.
RudomÃn P, Solodkin M, Jiménez I. Synaptic potentials of primary afferent fibers and motoneurons evoked by single intermediate nucleus interneurons in the cat spinal cord. J Neurophysiol 1987;57:1288–313.
Saadé NE, Tabet MS, Banna NR, Atweh SF, Jabbur SJ. Inhibition of nociceptive evoked activity in spinal neurons through a dorsal column-brain stem-spinal loop. Brain Res 1985;339:115–8.
Shimizu H, Shimoji K, Maruyama Y, Matsuki M, Kuribayashi H, Fujioka H. Human spinal cord potentials produced in lumbo-sacral enlargement by descending volleys. J Neurophysiol 1982;48:1108–20.
Shimoji K, Ito Y, Ohama K, Sawa T, Ikezono E. Presynaptic inhibition in man during anesthesia and sleep. Anesthesiology 1975;43:388–91.
Shimoji K, Matsuki M, Ito Y, Masuko K, Maruyama M, Iwane T, Aida S. Interactions of human cord dorsum potential. J Appl Physiol 1976;40:79–84.
Shimoji K, Matsuki M, Shimizu H. Wave-form characteristics and spatial distribution of evoked spinal electrogram in man. J Neurosurg 1977;46:304–13.
Shimoji K. Human spinal cord potentials (SCPs). Ascending recording variations-an update. In: Ducker TB, Brown RH, editors. Neurophysiology and standards of spinal cord monitoring. New York: Springer; 1986a. p. 19–28.
Shimoji K, Fujioka H, Maruyama Y, Hokari T, Takada T. Spinal cord potentials (SCPs) produced by descending volleys in the rat. In: Ducker TB, Brown RH, editors. Neurophysiology and standards of spinal cord monitoring, New York: Springer; 1986b. p. 73–81.
Shimoji K, Fujioka H, Maruyama Y, Shimizu H, Hokari T, Takada T. Spinal cord potentials (SCPs) produced by descending volleys in man. In: Ducker TB, Brown RH, editors. Neurophysiology and standards of spinal cord monitoring. New York: Springer; 1986c. p. 114–21.
Shimoji K, Fujiwara N, Fukuda S, Denda S, Takada T, Maruyama Y. Effects of isoflurane on spinal inhibitory potentials. Anesthesiology 1990;72:851–7.
Shimoji K, Sato Y, Denda S, Takada T, Fukuda S, Hokari T. Slow positive dorsal cord potentials activated by heterosegmental stimuli. Electroencephalogr Clin Neurophysiol 1992a;85:72–80.
Shimoji K, Fujiwara N, Denda S, Tomita M, Toyama M, Fukuda S. Effects of pentobarbital on heterosegmentally activated dorsal root depolarization in the rat: investigation by sucrosegap technique in vivo. Anesthesiology 1992b;76:958–66.
Shimoji K, Tomita M, Tobita T, Baba H, Takada T, Fukuda S, Aida S, Fujiwara N. Erb’s point stimulation produces slow positive potentials in human lumbar spinal cord. J Clin Neurophysiol 1994;11:365–74.
Sirkin DW, Feng AS. Autoradiographic study of descending pathways from the pontine reticular formation and the mesencephalic trigeminal nucleus in the rat. J Comp Neurol 1987;256:483–93.
Villanueva L, Peschanski M, Calvino B, Le Bars D. Ascending pathways in the spinal cord involved in triggering of diffuse noxious inhibitory controls in the rat. J Neurophysiol 1986;55:34–55.
Willis WD Jr. The raphe-spinal system. In: Barnes CD, editor. Brainstem control of spinal cord function. Orlando: Academic Press; 1984. p. 141–214.
Wolters JG, de Boer-Van Huizen R, Ten Donkelaar HJ, Leenen L. Collateralization of descending pathways from the brain-stem to the spinal cord in a lizard, varanus exanthematicus. J Comp Neurol 1986;251:317–33.
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2006 Springer-Verlag Tokyo
About this chapter
Cite this chapter
Tomita, M., Shimoji, K. (2006). Heterosegmental SCPs (HSPs). In: Shimoji, K., Willis, W.D. (eds) Evoked Spinal Cord Potentials. Springer, Tokyo. https://doi.org/10.1007/4-431-30901-2_8
Download citation
DOI: https://doi.org/10.1007/4-431-30901-2_8
Publisher Name: Springer, Tokyo
Print ISBN: 978-4-431-24026-6
Online ISBN: 978-4-431-30901-7
eBook Packages: MedicineMedicine (R0)