Physiological Changes during Recovery from a Primate Dorsal Column Lesion

References

• Andersson S. A., Norrsell K., Norrsell U. Spinal pathways projecting to the cerebral first somatosensory area in the monkey. J. Physiol. (Lond.) 1972; 225: 589–597
   Google Scholar
• Berkley K. J. 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. J. Comp. Neurol. 1980; 193: 283–317
   Google Scholar
• Berkley K. J., Vierck C. J., Jr. Reduced retrograde labeling of diencephalic-projecting neurons in the gracile nucleus of the monkey following removal of dorsal column input. Exp. Brain Res. 1993; 123: 64–73
   Google Scholar
• Bernstein J. J., Ganchrow D. Relationship of afferentation with soma size of nucleus gracilis neurons after bilateral dorsal column lesion in the rat. Exp. Neurol. 1981; 71: 452–463
   PubMed Web of Science ®Google Scholar
• Brown P. B., Busch G. R., Whittington J. Anatomical changes in cat dorsal horn cells after transection of a single dorsal root. Exp. Neurol. 1979; 64: 453–468
   PubMed Web of Science ®Google Scholar
• Calford M. B., Tweedale R. Acute changes in cutaneous receptive field in primary somatosensory cortex after digit denervation in adult flying fox. J. Neurophysiol. 1991; 65: 178–187
   PubMed Web of Science ®Google Scholar
• Cooper B. Y., Glendinnino D. S., Vierck C. J., Jr. Finger movement deficits in the stumptail macaque following lesions of the cuneate fasciculus. Somatosens. Mot. Res. 1992; 10: 17–30
   Web of Science ®Google Scholar
• Cusick J. F., Myklebust J. B., Larson S. J., Sances A. Spinal cord evaluation by cortical evoked responses. Arch. Neurol. 1979; 36: 140–143
   PubMedGoogle Scholar
• Decima E. E., Lorenzo D., Mallach L. Effects of “partial axotomy” upon synaptic function. Exp. Brain Res. 1986; 64: 464–468
   PubMed Web of Science ®Google Scholar
• Dietrich W. D., Ginsberg M. D., Busto R., Smith D. W. Metabolic alterations in rat somatosensory cortex following unilateral vibrissal removal. J. Neurosci. 1985; 5: 874–880
   PubMed Web of Science ®Google Scholar
• DeVito J. L., Ruch T. C., Patton H. D. Analysis of residual weight discriminatory ability and evoked potentials following section of dorsal columns in monkeys. Indian J. Physiol. Pharmacol. 1964; 8: 117–126
   PubMedGoogle Scholar
• Dostrovsky J. O., Millar J. Receptive fields of gracile neurons after transection of the dorsal columns. Exp. Neurol. 1977; 56: 610–621
   PubMed Web of Science ®Google Scholar
• Dreyer D. A., Schneider R. J., Metz C. B., Whitsel B. L. Differential contributions of spinal pathways to body representation in postcentral gyrus of Macaca mulatto. J. Neurophysiol. 1974; 37: 119–145
   PubMed Web of Science ®Google Scholar
• Eidelberg E., Woodbury C. M. Apparent redundancy in the somatosensory system in monkeys. Exp. Neurol. 1972; 37: 573–581
   PubMed Web of Science ®Google Scholar
• Enevoldson T. P., Gordon G. Spinocervical neurons and dorsal horn neurons projecting to the dorsal column nuclei through the dorsolateral fascicle: A retrograde HRP study in the cat. Exp. Brain Res. 1989; 75: 621–630
   PubMed Web of Science ®Google Scholar
• Gardner E., Morin F. Spinal pathways for projection of cutaneous and muscular afferents to the sensory and motor cortex of the monkey (Macaca mulatto). J. Physiol. (Lond.) 1953; 174: 149–154
   Google Scholar
• Gardner E., Morin F. Projection of fast afferents to the cerebral cortex of monkey. Am. J. Physiol. 1957; 189: 152–158
   PubMedGoogle Scholar
• Garraghty P. E., Kaas J. H. Functional reorganization in adult monkey thalamus after peripheral nerve injury. NeuroReport 1991; 2: 747–750
   PubMed Web of Science ®Google Scholar
• Glendinning D. S., Vierck C. J., Jr., Cooper B. Y. The effect of fasciculus cuneatus lesions on finger positioning and long-latency reflexes in monkeys. Exp. Brain Res. 1993; 93: 104–116
   PubMed Web of Science ®Google Scholar
• Kapadia S. E., LaMotte C. C. Deafferentation-induced alterations in the rat dorsal horn: I. Comparison of peripheral nerve injury vs. rhizotomy effects on presynaptic, postsynaptic and glial processes. J. Comp. Neurol. 1987; 266: 183–197
   Google Scholar
• Kelahan A. M., Doetsch G. S. Time-dependent changes in the functional organization of somatosensory cerebral cortex following digit amputation in adult raccoons. Somatosens. Res. 1984; 2: 49–81
   PubMed Web of Science ®Google Scholar
• Kjerulf T. D., O'Neal J. T., Calvin W. H., Loeser J. D., Westrum L. Deafferentation effects in lateral cuneate nucleus of the cat: Correlation of structural alterations with firing pattern changes. Exp. Neurol. 1973; 39: 86–102
   PubMed Web of Science ®Google Scholar
• Kulics A. T., Cauller L. J. Cerebral cortical somatosensory evoked responses, multiple unit activity and current source-densities: Their interrelationships and significance to somatic sensation as revealed by stimulation of the awake monkey's hand. Exp. Brain Res. 1986; 62: 46–60
   PubMed Web of Science ®Google Scholar
• LaMotte C. C., Kapadia S. E., Kocol C. M. Deafferentation-induced expansion of saphenous terminal field labeling in the adult rat dorsal horn following pronase injection of the sciatic nerve. J. Comp. Neurol. 1989; 288: 311–325
   PubMed Web of Science ®Google Scholar
• Loewy A. D. Transneuronal changes in the gracile nucleus. J. Comp. Neurol. 1973; 147: 497–510
   PubMed Web of Science ®Google Scholar
• Ma W., Peschanski M., Ralston H. J. The differential synaptic organization of the spinal and lemniscal projections to the ventrobasal complex of the rat thalamus: Evidence for convergence of the two systems upon single thalamic neurons. Neuroscience 1987; 22: 925–934
   PubMed Web of Science ®Google Scholar
• Mathews M. R., Cowan W. M., Powell T. P. S. Transneuronal cell degeneration in the lateral geniculate nucleus of the macaque monkey. J. Anat. (Lond.) 1960; 94: 145–169
   PubMed Web of Science ®Google Scholar
• McNeill D. L., Carlton S. M., Coogeshall R. E., Holsebosch C. E. Denervation-induced intraspinal synaptogenesis of calcitonin gene-related peptide containing primary afferent terminals. J. Comp. Neurol. 1990; 296: 263–268
   PubMed Web of Science ®Google Scholar
• Mendenhall W., Scheaffer R. L., Wackerly D. D. Mathematical Statistics with Applications, 3rd ed. Duxbury Press, Boston 1986
   Google Scholar
• Merzenich M. M., Kaas J. H., Wall J. T., Sur M., Nelson R. J., Felleman D. J. Progression of change following median nerve section in the cortical representation of the hand in areas 3b and 1 in adult owl and squirrel monkeys. Neuroscience 1983; 10: 639–665
   PubMed Web of Science ®Google Scholar
• Molander C., Honopaison J., Grant G. Changing pattern of C-fos expression in spinal cord neurons after electrical stimulation of the chronically injured sciatic nerve in the rat. Neuroscience 1992; 50: 223–236
   PubMed Web of Science ®Google Scholar
• Murray M., Goldberger M. E. Replacement of synaptic terminals in lamina II and Clarke's nucleus after unilateral lumbosacral dorsal rhizotomy in adult cats. J. Neurosci. 1986; 6: 3205–3217
   PubMed Web of Science ®Google Scholar
• Nelson R. J., Sur M., Kaas J. H. Representations of the body surface in postcentral parietal cortex of Macaca fascicularis. J. Comp. Neurol. 1980; 192: 459–470
   Web of Science ®Google Scholar
• Rausell E., Cusick C. G., Taub E., Jones E. G. Chronic deafferentation in monkeys differentially affects nociceptive and nonnociceptive pathways distinguished by specific calcium-binding proteins and down-regulates gamma-aminobutyric acid type A receptors at thalamic levels. Proc. Natl. Acad. Sci. USA 1992; 89: 2571–2575
   PubMed Web of Science ®Google Scholar
• Rustioni A., Hayes N. L., O'Neill S. Dorsal column nuclei and ascending spinal afferents in macaques. Brain 1979; 102: 95–125
   PubMed Web of Science ®Google Scholar
• Rustioni A., Sotelo C. Some effects of chronic deafferentation on the ultrastructure of the nucleus gracilis of the cat. Brain Res. 1974; 73: 527–533
   PubMed Web of Science ®Google Scholar
• Tessler A., Himes B. T., Soper K., Murray M., Goldberger M. E., Reichlin S. Recovery of substance P but not somatostatin in the cat spinal cord after unilateral lumbosacral dorsal rhizotomy: A quantitative study. Brain Res. 1984; 305: 95–102
   PubMed Web of Science ®Google Scholar
• Tommerdahl M., Whitsel B. L., Vierck C. J., Jr., Favorov O., Juuano S., Cooper B., Metz C., Nakhle B. The effects of spinal dorsal column transection on the SI response to repetitive skin stimulation. 1994, Manuscript submitted for publication.
   Google Scholar
• Vierck C. J., Jr. Alternations of spatio-tactile discrimination after lesions of primate spinal cord. Brain Res. 1973; 58: 69–79
   PubMed Web of Science ®Google Scholar
• Vierck C. J., Jr. Tactile movement detection and discrimination following dorsal column lesions in monkeys. Exp. Brain Res. 1974; 20: 311–346
   PubMed Web of Science ®Google Scholar
• Vierck C. J., Jr. Proprioceptive deficits after dorsal column lesions in monkeys. The Somatosensory System, H. H. Kornhuber. Georg Thieme, Stuttgart 1975; 310–317
   Google Scholar
• Vierck C. J., Jr. Absolute and differential sensitivities to touch stimuli after spinal cord lesions in monkeys. Brain Res. 1977; 134: 529–539
   PubMed Web of Science ®Google Scholar
• Vierck C. J., Jr. Comparison of forelimb and hindlimb motoric deficits following dorsal column section in monkeys. Brain Res. 1978; 146: 279–294
   PubMed Web of Science ®Google Scholar
• Vierck C. J., Jr. Comparison of the effects of dorsal rhizotomy and dorsal column section on motor performance of monkeys. Exp. Neurol. 1982a; 75: 566–575
   PubMed Web of Science ®Google Scholar
• Vierck C. J., Jr. Plasticity of somatic sensations and motor capabilities following lesions of the dorsal spinal columns in monkeys. Changing Concepts of the Nervous System, A. R. Morrison, P. L. Strick. Academic Press, New York 1982b; 151–169
   Google Scholar
• Vierck C. J., Jr., Cohen R. H., Cooper B. Y. Effects of spinal tractotomy on spatial sequence recognition in macaques. J. Neurosci. 1983; 3: 280–290
   PubMed Web of Science ®Google Scholar
• Vierck C. J., Jr., Cohen R. H., Cooper B. Y. Effects of spinal lesions on temporal resolution of cutaneous sensations. Somatosens. Res. 1985; 3: 45–56
   PubMed Web of Science ®Google Scholar
• Vierck C. J., Jr., Cooper B. Y. Epicritic sensations of primates. Comparative Perception, M. A. Berkley, W. C. Stebbins. Wiley, New York 1990; 29–66
   Google Scholar
• Vierck C. J., Jr., Whitsel B. L., Kulics A. T., Cooper B. Y. Alterations of a cortical network of neurons following interruption of the dorsal spinal columns. Advances in Neural Regeneration Research, F. Seil. Wiley-Liss, New York 1990; 355–368
   Google Scholar
• Wall J. T., Cusick C. G. Cutaneous responsiveness in primary somatosensory (S-I) hindpaw cortex before and after partial hind-paw deafferentation in adult rats. J. Neurosci. 1984; 4: 1499–1515
   PubMed Web of Science ®Google Scholar
• Wang S.-D., Goldberger M. E., Murray M. Plasticity of spinal systems after unilateral lumbosacral dorsal rhizotomy in the adult rat. J. Comp. Neurol. 1991; 304: 555–568
   PubMed Web of Science ®Google Scholar
• Warren R., Tremblay N., Dykes R. W. Quantitative study of glutamic acid decarboxylase-immunoreactive neurons and cytochrome oxidase activity in normal and partially deafferented rat hindlimb somatosensory cortex. J. Comp. Neurol. 1989; 288: 583–592
   PubMed Web of Science ®Google Scholar
• Wells J., Tripp L. N. Time course of reactive synaptogenesis in the subcortical somatosensory system, J. Comp. Neurol. 1987; 255: 466–475
   PubMed Web of Science ®Google Scholar
• Whitsel B. L., Favorov O. V., Kelly D. G., Tommerdahl M. Mechanisms of dynamic peri-and intra-columnar interactions in somatosensory cortex: Stimulus-specific contrast enhancement by NMDA receptor activation. Information Processing in the Somatosensory System, O. Franzen, J. Westman. Macmillan, London 1990; 1–17
   Google Scholar
• Whitsel B. W., Petrucelli L. M., Sapiro G. Modality representation in the lumbar and cervical fasciculus gracilis of squirrel monkey. Brain Res. 1969; 15: 67–78
   PubMed Web of Science ®Google Scholar
• York D. H. Somatosensory evoked potentials in man: Differentiation of spinal pathways responsible for conduction from the forelimb vs. Hindlimb. Prog. Neurobiol. 1985; 25: 1–25
   PubMed Web of Science ®Google Scholar