Nature Publishing Group, publisher of Nature, and other science journals and reference works
Nature
my account e-alerts subscribe register
SEARCH JOURNAL     advanced search
Journal Home
Current Issue
AOP
Archive
Download PDF
References
Export citation
Export references
Send to a friend
More articles like this

Letters to Nature
Nature 386, 495 - 498 (03 April 1997); doi:10.1038/386495a0

Deactivation and reactivation of somatosensory cortex after dorsal spinal cord injury

Neeraj Jain, Kenneth C. Catania & Jon H. Kaas

Department of Psychology, 301 Wilson Hall, Vanderbilt University, Nashville, Tennessee 37240, USA

Sensory stimuli to the body are conveyed by the spinal cord to the primary somatosensory cortex. It has long been thought that dorsal column afferents of the spinal cord represent the main pathway for these signals1–3, but the physiological and behavioural consequences of cutting the dorsal column have been reported to range from mild and transitory4–8 to marked9–13. We have re-examined this issue by sectioning the dorsal columns in the cervical region and recording the responses to hand stimulation in the contralateral primary somatosensory cortex (area 3b). Following a complete section of the dorsal columns, neurons in area 3b become immediately and perhaps permanently unresponsive to hand stimulation. Following a partial section, the remaining dorsal column afferents continue to activate neurons within their normal cortical target territories, but after five or more weeks the area of activation is greatly expanded. After prolonged recovery periods of six months or more, the deprived hand territory becomes responsive to inputs from the face (which are unaffected by spinal cord section). Thus, area 3b of somatosensory cortex is highly dependent on dorsal spinal column inputs, and other spinal pathways do not substitute for the dorsal columns even after injury.

  1. Mountcastle, V. B. Central nervous mechanisms in mechanoreceptive sensibility. In Handbook of Physiology—The Nervous System III (eds Darian-Smith, I) 789−878 (American Physiological Society, Bethesda, MD, 1984).
  2. Tommerdahl, M. et al. Effects of spinal dorsal column transection on the response of monkey anterior parietal cortex to repetitive skin stimulation. Cerebral Cortex 6, 131−155 (1996). | PubMed | ChemPort |
  3. Beck, C. H. M. Dual dorsal columns: a review. Can. J. Neurol. Sci. 3, 1−7 (1976). | PubMed | ChemPort |
  4. Andersson, S. A., Finger, S. & Norrsell, U. Cerebral units activated by tactile stimuli via a ventral spinal pathway in primates. Acta Physiol. Scand. 93, 119−128 (1975). | PubMed | ChemPort |
  5. Eidelberg, E., Kreinick, C. J. & Langescheid, C. On the possible role of afferent pathways in skin sensation. Exp. Neurol 47, 419−432 (1975). | Article | PubMed | ChemPort |
  6. Glendinning, D. S. & Vierck, C. J. Jr Lack of proprioceptive deficit after dorsal column lesions in monkeys. Neurology 43, 363−366 (1993). | PubMed | ChemPort |
  7. Wall, P. D. The sensory and motor role of impulses travelling in the dorsal columns towards cerebral cortex. Brain 93, 505−524 (1970). | PubMed | ChemPort |
  8. Vierck, C. J. Jr Alterations of spatio-tactile discrimination after lesions of primate spinal cord. Brain Res. 58, 69−79 (1973). | Article | PubMed |
  9. Dreyer, D. A., Schneider, R. J., Metz, C. B. & Whitsel, B. L. Differential contributions of spinal pathways to body representation in post central gyrus of Macaca mulatta. J. Neurophysiol. 37, 119−145 (1974). | PubMed | ChemPort |
  10. Glendinning, D. S., Vierck, J. C. J. & Cooper, B. Y. The effect of fasciculus cuneatus lesions on finger positioning and long latency reflexes in monkeys. Exp. Brain Res. 93, 104−116 (1993). | PubMed | ChemPort |
  11. Glendinning, D. S., Cooper, B. Y., Vierck, C. J. Jr & Leonard, C. M. Altered precision grasping in stumptail macaques after fasciculus cuneatus lesions. Somatosens. Motor Res. 9, 61−73 (1991).
  12. Schneider, R. J. Loss of information concerning hair displacement and other somatic stimuli in the first somatic sensory cortex of unanesthetized macaca mulatta monkeys following dorsal funiculus transections. Exp. Brain Res. 83, 105−114 (1990). | PubMed | ChemPort |
  13. Vierck, C. J. Jr, Cohen, R. H. & Cooper, B. Y. Effects of spinal lesions on temporal resolution of cutaneous sensations. Somatosensory Res. 3, 45−56 (1985).
  14. Kaas, J. H. Plasticity of sensory and motor maps in adult mammals. Annu. Rev. Neurosc. 14, 137−167 (1991). | ChemPort |
  15. Merzenich, M. M. et al. Topographic reorganization of somatosensory cortical areas 3B and 1 in adult monkeys following restricted deafferentation. Neuroscience 8, 33−55 (1983). | Article | PubMed | ISI | ChemPort |
  16. Kaas, J. H. What if anything is S1? The organization of the "first somatosensory area" of cortex. Physiol. Rev. 63, 206−231 (1983). | PubMed | ISI | ChemPort |
  17. Jain, N., Catania, K. C. & Kaas, J. H. An anatomical isomorph of the hand in somatosensory cortex of owl monkeys and its immutability following peripheral deafferentation. Soc. Neuro. Sci. Abstr 22, 1054 (1996).
  18. Florence, S. L. & Kaas, J. H. Large-scale organization at multiple levels of the somatosensory pathway follows therapeutic amputation of the hand in monkeys. J. Neurosci. 15, 8083−8095 (1995). | PubMed | ISI | ChemPort |
  19. Jain, N., Florence, S. L. & Kaas, J. H. Limits on plasticity in somatosensory cortex of adult rats: hindlimb cortex is not reactivated after dorsal column section. J. Neurophysiol. 73, 1537−1546 (1995). | PubMed | ChemPort |
  20. Florence, S. L., Wall, J. T. & Kaas, J. H. Somatotopic organization of inputs from the hand to the spinal gray and cuneate nucleus of monkeys with observations on the cuneate nucleus of humans. J. Comp. Neurol. 286, 48−70 (1989). | Article | PubMed | ChemPort |
  21. Merzenich, M. M., Kaas, J. H., Sur, M. & Lin, C. S. Double representation of the body surface within cytoarchitectonic areas 3b and 1 in 'SI' in the owl monkey (Aorus trivirgatus). J. Comp. Neurol. 181, 41−73 (1978). | Article | PubMed | ChemPort |
  22. Florence, S. L., Wall, J. T. & Kaas, J. H. Central projections from the skin of the hand in squirrel monkeys. J. Comp. Neurol. 311, 563−578 (1991). | Article | PubMed | ChemPort |
  23. Pons, T. P. et al. Massive cortical reorganization after sensory deafferentation in adult macaques. Science 252, 1857−1860 (1991). | PubMed | ISI | ChemPort |
  24. Sweet, W. H. 'Phantom' sensations following intraspinal injury. Neurochirurgia 18, 139−154 (1975). | PubMed | ChemPort |
  25. Davis, R. W. Phantom sensation, phantom pain, and stump pain. Arch. Phys. Med. Rhabil. 74, 79−91 (1993). | ChemPort |
  26. Gallyas, F. Silver staining of myelin by means of physical development. Neurol. Res. 1, 203−209 (1979). | PubMed | ChemPort |
  27. Gibson, A. R., Hansama, D. I. & Robinson, F. R. A sensitive low artifact TMB procedure for the demonstration of WGA-HRP in the CNS. Brain Res. 298, 235−241 (1984). | Article | PubMed | ChemPort |
  28. Wong-Riley, M. T. T. Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry. Brain Res. 171, 11−28 (1979). | Article | PubMed | ChemPort |



© 1997 Nature Publishing Group
Privacy Policy