Changes in the Spinal Terminal Pattern of the Superficial Radial Nerve After A Peripheral Nerve Injury: An Anatomical Study in Cats

References

• Abrahams V C, Swett J E. The pattern of spinal and medullary projections from a cutaneous nerve and a muscle nerve of the forelimb of the cat: a study using the transganglionic transport of HRP. J Comp Neurol 1986; 246: 70–84
   PubMedGoogle Scholar
• Aldskogius H, Arvidsson J, Grant G. The reaction of primary sensory neurons to peripheral nerve injury with particular emphasis on transganglionic changes. Brain Res 1985; 357: 27–46
   PubMedGoogle Scholar
• Arvidsson J, Johansson K. Changes in the central projection pattern of vibrissae innervating primary sensory neurons after peripheral nerve injury in the rat. Neurosci Lett 1988; 84: 20–24
   Google Scholar
• Arvidsson J, Ygge J, Grant G. Cell loss in lumbar dorsal root ganglia and transganglionic degeneration after sciatic nerve resection in the rat. Brain Res 1986; 373: 15–21
   PubMed Web of Science ®Google Scholar
• Basbaum A I, Wall P D. Chronic changes in the response in cells in adult cat dorsal horn following partial deafferentation: the appearance of responding cells in a previously nonresponsive region. Brain Res 1976; 116: 181–204
   PubMed Web of Science ®Google Scholar
• Bowe C M, Hildebrand C, Koosis J D, Waxman S G. Morphological and physiological properties of neurons after long-term axonal regeneration: observations on chronic and delayed sequelae of peripheral nerve injury. J Neurol Sci 1989; 91: 259–292
   PubMed Web of Science ®Google Scholar
• Brown A G, Fyffe R E, Noble R, Rowe M J. Effects of hind limb nerve section on lumbosacral dorsal horn neurones in the cat. J Physiol (Lond) 1984; 354: 375–394
   Google Scholar
• Brushart T M. Preferential reinnervation of motor nerves by regenerating motor axons. J Neurosci 1988; 8: 1026–1031
   PubMed Web of Science ®Google Scholar
• Brushart T M, Mesulam M M. Transganglionic demonstration of central sensory projections from skin and muscle with HRP-lectin conjugates. Neurosci Lett 1980; 17: 1–6
   PubMedGoogle Scholar
• Coderre T J, Katz J, Vaccarino A L, Melzack R. Contribution of central neuroplasticity to pathological pain: review of clinical and experimental evidence. Pain 1993; 52: 259–285
   PubMed Web of Science ®Google Scholar
• Devor M, Govrin-Lippmann R, Frank I, Raber P. Proliferation of primary sensory neurons in adult rat dorsal root ganglion and the kinetics of retrograde cell loss after sciatic nerve section. Somatosens Res 1985; 3: 139–167
   PubMed Web of Science ®Google Scholar
• Devor M, Wall P D. Reorganisation of spinal cord sensory map after peripheral nerve injury. Nature 1978; 276: 75–76
   PubMed Web of Science ®Google Scholar
• Dykes R W. Central consequences of peripheral nerve injuries. Ann Plast Surg 1984; 13: 412–422
   PubMed Web of Science ®Google Scholar
• Finger S, Almli C R. Brain damage and neu-roplasticity: mechanisms of recovery or development?. Brain Res 1985; 357: 177–186
   PubMed Web of Science ®Google Scholar
• Fitzgerald M. The sprouting of saphenous nerve terminals in the spinal cord following early postnatal sciatic nerve section in the rat. J Comp Neurol 1985; 240: 407–413
   PubMed Web of Science ®Google Scholar
• Fitzgerald M, Woolf C J, Shortland P. Collateral sprouting of the central terminals of cutaneous primary afferent neurons in the rat spinal cord: pattern, morphology, and influence of targets. J Comp Neurol 1990; 300: 370–385
   PubMed Web of Science ®Google Scholar
• Gonatas N K, Harper C, Mizutani T, Gonatas J O. Superior sensitivity of conjugates of horseradish peroxidase with wheat germ agglutinin for studies of retrograde axonal transport. J Histochem Cytochem 1979; 27: 728–734
   PubMed Web of Science ®Google Scholar
• Grant G, Arvidsson J, Robertson B, Ygge J. Transganglionic transport of horseradish peroxidase in primary sensory neurons. Neurosci Lett 1979; 12: 23–28
   PubMed Web of Science ®Google Scholar
• Heimer L, Zaborszky L. Neuroanatomical tract-tracing methods 2. Plenum Press, Recent progress. New York, London 1989
   Google Scholar
• Johnson E M, Jr, Rich K M, Yip H K. The role of NGF in sensory neurons in vivo. Trends Neurosci 1986; 1: 33–37
   Google Scholar
• Kaas J H. Plasticity of sensory and motor maps in adult mammals. Annu Rev Neurosci 1991; 14: 137–167
   PubMed Web of Science ®Google Scholar
• Kapadia S E, LaMotte C C. Deafferentiation-induced alterations in the rat dorsal horn: I. Comparison of peripheral nerve injury vs. rhi-zotomy effects on presynaptic, postsynaptic, and glial processes. J Comp Neurol 1987; 266: 183–197
   PubMedGoogle Scholar
• Koerber H R. Somatotopic organization of cat brachial cord. Exp Neurol 1980; 69: 481–492
   PubMedGoogle Scholar
• Koerber H R, Seymour A W, Mendell L M. Mismatches between peripheral receptor type and central projections after peripheral nerve regeneration. Neurosci Lett 1989; 99: 67–72
   PubMed Web of Science ®Google Scholar
• LaMotte C C, Kapadia S E. Deafferentation-induced alterations in the rat dorsal horn: II. Effects of selective poisoning by pronase of the central processes of a peripheral nerve. J Comp Neurol 1987; 266: 198–208
   PubMedGoogle Scholar
• LaMotte C C, Kapadia S E, Kocol C M. Deafferentation-induced expansion of saphenous terminal field labelling 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
• Lisney S J. Changes in the somatotopic organization of the cat lumbar spinal cord following peripheral nerve transsection and regeneration. Brain Res 1983; 259: 31–39
   PubMed Web of Science ®Google Scholar
• Lisney S J. The cat lumbar spinal cord somatotopic map is unchanged after peripheral nerve crush and regeneration. Brain Res 1983; 271: 166–169
   PubMedGoogle Scholar
• Liss A G, af Ekenstam F W, Wiberg M. Cell loss in sensory ganglia after peripheral nerve injury. An anatomical tracer study using lectin-coupled horseradish peroxidase in cats. Scand J Plast Reconstr Hand Surg 1994; 28: 177–188
   PubMed Web of Science ®Google Scholar
• Litchy W J. Uptake and retrograde transport of horseradish peroxidase in frog sartorius nerve in vitro. Brain Res 1973; 56: 377–381
   PubMedGoogle Scholar
• Liuzzi F J, Tedeschi B. Peripheral nerve regeneration. Neurosurg Clin N Am 1991; 2: 31–42
   PubMedGoogle Scholar
• Lundborg G. Nerve regeneration and repair. A review. Acta Orthop Scand 1987; 58: 145–169
   PubMed Web of Science ®Google Scholar
• Lunn E R, Brown M C, Perry V H. The pattern of axonal degeneration in the peripheral nervous system varies with different types of lesion. Neuroscience 1990; 35: 157–165
   PubMedGoogle Scholar
• Markus H, Pomeranz B, Krushelnycky D. Spread of saphenous somatotopic projection map in spinal cord and hypersensitivity of the foot after chronic sciatic denervation in adult rat. Brain Res 1984; 296: 27–39
   PubMed Web of Science ®Google Scholar
• Mesulam M M. Tetramethyl benzidine for horseradish peroxidase neurohistochemistry: a non-carcinogenic blue reaction product with superior sensitivity for visualizing neural afferents and efferents. J Histochem Cytochem 1978; 26: 106–117
   PubMed Web of Science ®Google Scholar
• Molander C, Kinnman E, Aldskogius H. Expansion of spinal cord primary sensory afferent projection following combined sciatic nerve resection and saphenous nerve crush: a horseradish peroxidase study in the adult rat [published erratum appears in. J Comp Neurol 1989; 286: 541, ].J Comp Neurol 1988; 276: 436–441
   Google Scholar
• Nyberg G, Blomqvist A. The somatotopic organization of forelimb cutaneous nerves in the brachial dorsal horn: an anatomical study in the cat. J Comp Neurol 1985; 242: 28–39
   PubMedGoogle Scholar
• Orgel M G, O'Brien W J, Murray H M. Pulsing electromagnetic field therapy in nerve regeneration: an experimental study in the cat. Plast Reconstr Surg 1984; 73: 173–183
   PubMed Web of Science ®Google Scholar
• Otto D, Unsicker K, Grothe C. Pharmacological effects of nerve growth factor and fibroblast growth factor applied to the transectioned sciatic nerve on neuron death in adult rat dorsal root ganglia. Neurosci Lett 1987; 83: 156–160
   PubMed Web of Science ®Google Scholar
• Peyronnard J M, Charron L. Decreased horseradish peroxidase labeling in deafferented spinal motoneurons of the rat. Brain Res 1983; 275: 203–214
   PubMedGoogle Scholar
• Pubols L M. The boundary of proximal hindlimb representation in the dorsal horn following peripheral nerve lesions in cats: a reevaluation of plasticity in the somatotopic map. Somatosens Res 1984; 2: 19–32
   PubMed Web of Science ®Google Scholar
• Pubols L M, Bowen D C. Lack of central sprouting of primary afferent fibers after ricin deafferentation. J Comp Neurol 1988; 275: 282–287
   PubMedGoogle Scholar
• Raji A R, Bowden R E. Effects of high-peak pulsed electromagnetic field on the degeneration and regeneration of the common peroneal nerve in rats. J Bone Joint Surg [Br] 1983; 65: 478–492
   PubMed Web of Science ®Google Scholar
• Rexed B. The cytoarchitectonic organization of the spinal cord in the cat. J Comp Neurol 1952; 96: 415–495
   Web of Science ®Google Scholar
• Rich K M, Luszczynski J R, Osborne P A, Johnson E MJ. Nerve growth factor protects adult sensory neurons from cell death and atrophy caused by nerve injury. J Neurocytol 1987; 16: 261–268
   PubMedGoogle Scholar
• Richardson P M, Issa V M. Peripheral injury enhances central regeneration of primary sensory neurones. Nature 1984; 309: 791–793
   PubMed Web of Science ®Google Scholar
• Rodin B E, Sampogna S L, Kruger L. An examination of intraspinal sprouting in dorsal root axons with the tracer horseradish peroxidase. J Comp Neurol 1983; 215: 187–198
   PubMedGoogle Scholar
• Rosene D L, Mesulam M M. Fixation variables in horseradish peroxidase neurohistochemistry. I. The effect of fixation time and perfusion procedures upon enzyme activity. J Histochem Cyto-chem 1978; 26: 28–39
   Google Scholar
• Seltzer Z, Devor M. Effect of nerve section on the spinal distribution of neighbouring nerves. Brain Res 1984; 306: 31–37
   PubMedGoogle Scholar
• Singer W, Holländer H, Vanegas H. Decreased peroxidase labeling of lateral geniculate neurons following deafferentation. Brain Res 1977; 120: 133–137
   PubMedGoogle Scholar
• Snow P J, Wilson P. Plasticity of somatosensory maps in the adult mammalian spinal cord. Soc Neurosci Abstract 1985; 11: 965
   Google Scholar
• Sugimoto T, Gobel S. Primary neurons maintain their central axonal arbors in the spinal dorsal horn following peripheral nerve injury: an anatomical analysis using transganglionic transport of horseradish peroxidase. Brain Res 1982; 248: 377–381
   PubMedGoogle Scholar
• Sugimoto T, Bennett G J, Kajander K C. Transsy-naptic degeneration in the superficial dorsal horn after sciatic nerve injury: effects of a chronic constriction injury, transection, and strychnine. Pain 1990; 42: 205–213
   PubMed Web of Science ®Google Scholar
• Trojanowski J Q. Native and derivatized lectins for in vivo studies of neuronal connectivity and neuronal cell biology. J Neurosci Methods 1983; 9: 185–204
   PubMed Web of Science ®Google Scholar
• Villar M J, Cortes R, Theodorsson E, et al. Neuropeptide expression in rat dorsal root ganglion cells and spinal cord after peripheral nerve injury with special reference to galanin. Neu-roscience 1989; 33: 587–604
   Google Scholar
• Wilson P. Absence of mediolateral reorganization of dorsal horn somatotopy after peripheral deafferentation in the cat. Exp Neurol 1987; 95: 432–447
   PubMed Web of Science ®Google Scholar
• Ygge J. On the organization of the thoracic spinal ganglion and nerve in the rat. Exp Brain Res 1984; 55: 395–401
   PubMed Web of Science ®Google Scholar