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

1. The responses of thirty‐five spinothalamic tract (s.t.t.) cells in or near lamina I of the dorsal horn were examined in chloralose‐ and barbiturate‐anaesthetized monkeys (Macaca fascicularis). Many of the cells could be classified on the basis of receptive field properties as either wide dynamic range (w.d.r.) cells or as high‐threshold (h.t.) cells. 2. Thalamic stimulation sites for antidromic activation of the s.t.t. cells were in or around the ventral posterior lateral nucleus. Axons of the s.t.t. cells had a mean conduction velocity of 17 m/s (33 and 14 m/s for w.d.r. and h.t. cells, respectively). Mean minimum afferent conduction velocity averaged 37 m/s (52 and 23 m/s for w.d.r. and h.t. cells, respectively). Background activity was low (mean of 2.3 impulses/s). 3. An alternative classification of the cells was based on a kappa means cluster analysis of the responses to a series of mechanical stimuli. The response profiles for a given cell were normalized, and those of the s.t.t. cells in or near lamina I were analysed along with the responses of a population of s.t.t. cells, largely in laminae IV‐VI, that had been described previously. S.t.t. cells in or near lamina I were distributed amongst three of the four groups of cells determined by the cluster analysis (types 2‐4). 4. Vibratory stimuli excited most of the w.d.r. but none of the h.t. cells tested. Best frequencies were 5‐10 Hz (at 100 and 500 microns indentations). 5. Most w.d.r. but few h.t. cells responded to cutaneous cooling. All of the cells responded to noxious heating, but w.d.r. cells had steeper stimulus‐response curves. 6. After a series of noxious heat stimuli, the thresholds for noxious heat were lowered and responses to lower‐intensity noxious heat stimuli were enhanced (sensitization). However, responses to more intense stimuli were reduced (inactivation). Similar changes were seen in the responses to graded mechanical stimuli. 7. It is concluded that s.t.t. cells in or near lamina I can signal noxious cutaneous stimuli but have poor coding abilities for innocuous mechanical stimuli. Some of these cells respond to innocuous thermal stimuli, but their role in thermoreception is unclear. The small receptive fields suggest that these cells could contribute to stimulus localization.

[1]  W. Willis,et al.  Temporal features of the responses of primate spinothalamic neurons to noxious thermal stimulation of hairy and glabrous skin. , 1986, Journal of neurophysiology.

[2]  A. Craig,et al.  Spinothalamic lumbosacral lamina I cells responsive to skin and muscle stimulation in the cat. , 1985, The Journal of physiology.

[3]  George L. Wilcox,et al.  An instrument using a multiple layer peltier device to change skin temperature rapidly , 1984, Brain Research Bulletin.

[4]  C. Woolf,et al.  The properties of neurones recorded in the superficial dorsal horn of the rat spinal cord , 1983, The Journal of comparative neurology.

[5]  P. Wall,et al.  A system of rat spinal cord lamina 1 cells projecting through the contralateral dorsolateral funiculus , 1983, The Journal of comparative neurology.

[6]  D. R. Kenshalo,et al.  Facilitation of the responses of primate spinothalamic cells to cold and to tactile stimuli by noxious heating of the skin , 1982, PAIN®.

[7]  W. Willis,et al.  Spinothalamic tract neurons that project to medial and/or lateral thalamic nuclei: evidence for a physiologically novel population of spinal cord neurons. , 1981, Journal of neurophysiology.

[8]  C. Anderson,et al.  A simple and rapid method for making carbon fiber microelectrodes , 1981, Journal of Neuroscience Methods.

[9]  K. Berkley,et al.  Spatial relationships between the terminations of somatic sensory and motor pathways in the rostral brainstem of cats and monkeys. I. Ascending somatic sensory inputs to lateral diencephalon , 1980, The Journal of comparative neurology.

[10]  D. Ferrington,et al.  Tactile neuron classes within second somatosensory area (SII) of cat cerebral cortex. , 1980, Journal of neurophysiology.

[11]  William D. Willis,et al.  The cells of origin of the primate spinothalamic tract , 1979, The Journal of comparative neurology.

[12]  M. Armstrong‐James,et al.  Carbon fibre microelectrodes , 1979, Journal of Neuroscience Methods.

[13]  W. Willis,et al.  Excitation of primate spinothalamic neurons by cutaneous C-fiber volleys. , 1979, Journal of neurophysiology.

[14]  W. Willis,et al.  Responses of primate spinothalamic neurons to graded and to repeated noxious heat stimuli. , 1979, Journal of neurophysiology.

[15]  J. Boivie An anatomical reinvestigation of the termination of the spinothalamic tract in the monkey , 1979, The Journal of comparative neurology.

[16]  C. Vierck,et al.  Loss and recovery of reactivity to noxious stimuli in monkeys with primary spinothalamic cordotomies, followed by secondary and tertiary lesions of other cord sectors. , 1979, Brain : a journal of neurology.

[17]  D. Ferrington,et al.  Coding of information about tactile stimuli by neurones of the cuneate nucleus. , 1978, The Journal of physiology.

[18]  R. Dubner,et al.  Spatial and temporal transformations of input to spinothalamic tract neurons and their relation to somatic sensations. , 1978, Journal of neurophysiology.

[19]  R. Dubner,et al.  Neurons that subserve the sensory-discriminative aspects of pain , 1977, Pain.

[20]  W. Willis,et al.  Spinal cord potentials evoked by cutaneous afferents in the monkey. , 1977, Journal of neurophysiology.

[21]  P. Wall,et al.  Diverse sensory functions with an almost totally divided spinal cord. A case of spinal cord transection with preservation of part of one anterolateral quadrant , 1976, Pain.

[22]  Ainsley Iggo,et al.  Nociceptor-driven dorsal horn neurones in the lumbar spinal cord of the cat , 1976, Pain.

[23]  J. B. Ranck,et al.  Which elements are excited in electrical stimulation of mammalian central nervous system: A review , 1975, Brain Research.

[24]  E. Carstens,et al.  Confirmation of the location of spinothalamic neurons in the cat and monkey by the retrograde transport of horseradish peroxidase , 1975, Brain Research.

[25]  P. R. Burgess,et al.  Ascending projections from marginal zone (Lamina I) neurons of the spinal dorsal horn , 1975 .

[26]  F. W. Kerr The ventral spinothalamic tract and other ascending systems of the ventral funiculus of the spinal cord , 1975, The Journal of comparative neurology.

[27]  William D. Willis,et al.  Responses of primate spinothalamic tract neurons to natural stimulation of hindlimb. , 1974 .

[28]  E. Perl,et al.  Spinal neurons specifically excited by noxious or thermal stimuli: marginal zone of the dorsal horn. , 1970, Journal of neurophysiology.

[29]  J. T. Eayrs,et al.  A Stereotaxic Atlas of the Java Monkey Brain , 1968 .

[30]  V. Mountcastle,et al.  The sense of flutter-vibration: comparison of the human capacity with response patterns of mechanoreceptive afferents from the monkey hand. , 1968, Journal of neurophysiology.

[31]  T. R. Shantha,et al.  A stereotaxic atlas of the Java monkey brain (Macaca irus) , 1967 .

[32]  D. Bowsher The termination of secondary somatosensory neurons within the thalamus of Macaca mulatta: An Experimental Degeneration Study , 1961, The Journal of comparative neurology.

[33]  W. Nauta,et al.  Ascending axon degeneration following anterolateral cordotomy. An experimental study in the monkey. , 1960, Brain : a journal of neurology.

[34]  B. Rexed,et al.  A cytoarchitectonic atlas of the spinal coed in the cat , 1954, The Journal of comparative neurology.

[35]  G Mann,et al.  ON THE THALAMUS * , 1905, British medical journal.

[36]  W D Willis,et al.  Classification of primate spinothalamic and somatosensory thalamic neurons based on cluster analysis. , 1986, Journal of neurophysiology.

[37]  W. Willis,et al.  Responses of primate spinothalamic neurons to noxious thermal stimulation of glabrous and hairy skin. , 1986, Journal of neurophysiology.

[38]  R. Dubner,et al.  Physiology and morphology of substantia gelatinosa neurons intracellularly stained with horseradish peroxidase. , 1980, The Journal of comparative neurology.

[39]  W D Willis,et al.  Responses of primate spinothalamic tract neurons to electrical stimulation of hindlimb peripheral nerves. , 1975, Journal of neurophysiology.

[40]  J. Chubbuck Small motion biological stimulator , 1966 .