Plasticity in the spinal cord sensory map following peripheral nerve injury in rats

The medial part of the L4 and 5 dorsal horn in adult rats is dominated by afferents from the toes and foot. After transection of the sciatic and saphenous nerves, virtually all cells in this region are left without any peripheral receptive field. Beginning 4 to 5 days after nerve section, however, many peripherally deafferented cells take on a novel receptive field on the thigh, lower back, or perineum. The new receptive fields are served by intact nerves ending in proximal skin rather than by misdirected sprouts of cut toe-foot nerves. Thus, peripheral axotomy results in synaptic reorganization in the spinal cord proper. Receptive field reorganization occurs after nerve transection, ligation, or ligation with distal transection but does not occur if the nerve is crushed. If a cut nerve is sutured and regeneration is permitted, spinal reorganization is reversed and the toe-foot afferents regain exclusive dominance of the medial dorsal horn.

[1]  H. Gainer,et al.  Retrograde axonal transport of endogenous proteins in sciatic nerve demonstrated by covalent labeling in vivo. , 1980, Science.

[2]  D Schonfeld,et al.  Two modes of cutaneous reinnervation following peripheral nerve injury , 1979, The Journal of comparative neurology.

[3]  P. Wall,et al.  Chronic changes in the response of cells in adult cat dorsal horn following partial deafferentation: The appearance of responding cells in a previously nonresponsive region , 1976, Brain Research.

[4]  Experimental model of regeneration in the central nervous system. I. Synaptic changes. , 1973, Brain : a journal of neurology.

[5]  M. Devor,et al.  Ongoing activity in severed nerves: source and variation with time , 1978, Brain Research.

[6]  B. Grafstein The nerve cell body response to axotomy , 1975, Experimental Neurology.

[7]  P. Brown,et al.  Somatotopic representation of hindlimb skin in cat dorsal horn. , 1975, Journal of neurophysiology.

[8]  W. Chambers,et al.  Intraspinal sprouting of dorsal root axons; development of new collaterals and preterminals following partial denervation of the spinal cord in the cat. , 1958, A.M.A. archives of neurology and psychiatry.

[9]  M. Devor,et al.  Type of sensory nerve fibre sprouting to form a neuroma , 1976, Nature.

[10]  P. Wall,et al.  The effect of peripheral nerve injury on dorsal root potentials and on transmission of afferent signals into the spinal cord , 1981, Brain Research.

[11]  W. E. Watson Cellular responses to axotomy and to related procedures. , 1974, British medical bulletin.

[12]  P. Wall,et al.  Effect of peripheral nerve injury on receptive fields of cells in the cat spinal cord , 1981 .

[13]  P. Wall,et al.  Dorsal horn cells in spinal and in freely moving rats. , 1967, Experimental neurology.

[14]  A. Dahlström,et al.  The effect of different types of axonal trauma on the synthesis and transport of amine storage granules in rat sciatic nerves. , 1973, Journal of neurobiology.

[15]  P. Wall,et al.  The response of rat spinal cord cells to unmyelinated afferents after peripheral nerve section and after changes in substance p levels , 1981, Neuroscience.

[16]  M. Devor,et al.  Mapping and plasticity of acid phosphatase afferents in the rat dorsal horn , 1980, Brain Research.

[17]  P. Wall,et al.  The physiology and anatomy of long ranging afferent fibres within the spinal cord. , 1976, The Journal of physiology.

[18]  Maturation of axonal sprouts after nerve crush , 1979, Experimental Neurology.

[19]  M. Goldberger,et al.  Restitution of function and collateral sprouting in the cat spinal cord: The deafferented animal , 1974, The Journal of comparative neurology.

[20]  Patrick D. Wall,et al.  Ongoing activity in peripheral nerves: The physiology and pharmacology of impulses originating from a neuroma ☆ , 1974 .