Peripheral nerve regeneration: An overview

Encyclopedia of Neuroscience

Volumn , Issue , 2009, Pages 557-560

  Richardson, P M ^a  

^a QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84869086849     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-008045046-9.00022-X     Document Type: Chapter

References (32)

1. Bareyre F.M., Kerschensteiner M., Raineteau O., et al. The injured spinal cord spontaneously forms a new intraspinal circuit in adult rats. Nature Neuroscience 2004, 7:269-277.
2. Barnett S.C., Riddell J.S. Olfactory ensheathing cells (OECs) and the treatment of CNS injury: Advantages and possible caveats. Journal of Anatomy 2004, 204:57-67.
3. Bjorklund A., Stenevi U. Reconstruction of the nigrostriatal dopamine pathway by intracerebral nigral transplants. Brain Research 1979, 177:555-560.
4. Bonilla I.E., Tanabe K., Strittmatter S.M. Small proline-rich repeat protein 1A is expressed by axotomized neurons and promotes axonal outgrowth. Journal of Neuroscience 2002, 22:1303-1315.
5. Bradley W.G., Asbury A.K. Duration of synthesis phase in neuilemma cells in mouse sciatic nerve during degeneration. Experimental Neurology 1970, 26:275-282.
6. Brushart T.M., Gerber J., Kessens P., et al. Contributions of pathway and neuron to preferential motor reinnervation. Journal of Neuroscience 1998, 18:8674-8681.
7. D'Antonio M., Michalovich D., Paterson M., et al. Gene profiling and bioinformatic analysis of Schwann cell embryonic development and myelination. Glia 2006, 53:501-515.
8. Dahlin L.B. Prevention of macrophage invasion impairs regeneration in nerve grafts. Brain Research 1995, 679:274-280.
9. Dailey A.T., Avellino A.M., Benthem L., et al. Complement depletion reduces macrophage infiltration and activation during Wallerian degeneration and axonal regeneration. Journal of Neuroscience 1998, 18:6713-6722.
10. Fu S.Y., Gordon T. Contributing factors to poor functional recovery after delayed nerve repair: Prolonged axotomy. Journal of Neuroscience 1995, 15:3876-3885.
11. Fu S.Y., Gordon T. Contributing factors to poor functional recovery after delayed nerve repair: Prolonged denervation. Journal of Neuroscience 1995, 15:3886-3895.
12. Goldberger M.E., Growdon J.H. Pattern of recovery following cerebellar deep nuclear lesions in monkeys. Experimental Neurology 1973, 39:307-322.
13. Heumann R., Lindholm D., Bandtlow C., et al. Differential regulation of mRNA encoding nerve growth factor and its receptor in rat sciatic nerve during development, degeneration, and regeneration: Role of macrophages. Proceedings of the National Academy of Sciences of the United States of America 1987, 84:8735-8739.
14. Kobayashi N.R., Fan D.-P., Giehl K.M., et al. BDNF and NT-4/5 prevent atrophy of rat rubrospinal neurons after cervical axotomy, stimulate GAP-43 and T?1-tubulin mRNA expression, and promote axonal regeneration. Journal of Neuroscience 1997, 17:9583-9595.
15. Li Y., Decherchi P., Raisman G. Transplantation of olfactory ensheathing cells into spinal cord lesions restores breathing and climbing. Journal of Neuroscience 2003, 23:727-731.
16. Lindvall O., Sawle G., Widner H., et al. Evidence for long-term survival and function of dopaminergic grafts in progressive Parkinson's disease. Annals of Neurology 1994, 35:172-180.
17. Lu X., Richardson P.M. Responses of macrophages in rat dorsal root ganglia following peripheral nerve injury. Journal of Neurocytology 1993, 22:334-341.
18. Malessy M.J., Bakker D., Dekker A.J., et al. Functional magnetic resonance imaging and control over the biceps muscle after intercostal-musculocutaneous nerve transfer. Journal of Neurosurgery 2003, 98:261-268.
19. McQuarrie I.G., Grafstein B. Axon outgrowth enhanced by a previous nerve injury. Archives of Neurology 1973, 29:53-55.
20. Moreno D.E., Yu X.-J., Goshgarian H.G. Identification of the axon pathways which mediate functional recovery of a paralyzed hemidiaphragm following spinal cord hemisection in the adult rat. Experimental Neurology 1992, 116:219-228.
21. Mueller M., Leonhard C., Wacker K., et al. Macrophage response to peripheral nerve injury: The quantitative contribution of resident and hematogenous macrophages. Laboratory Investigation 2003, 83:175-185.
22. Nguyen Q.T., Sanes J.R., Lichtman J.W. Pre-existing pathways promote precise projection patterns. Nature Neuroscience 2002, 5:861-867.
23. Raisman G. Neuronal plasticity in the septal nuclei of the adult rat. Brain Research 1969, 14:25-48.
24. Richardson P.M., Issa V.M.K. Peripheral injury enhances central regeneration of primary sensory neurons. Nature 1984, 309:791-793.
25. Richardson P.M., McGuinness U.M., Aguayo A.J. Axons from CNS neurones regenerate into PNS grafts. Nature 1980, 284:264-265.
26. Rossignol S., Bouyer L., Langlet C., et al. Determinants of locomotor recovery after spinal injury in the cat. Progress in Brain Research 2004, 143:163-172.
27. Sabel B.A., Schneider G.E. The principle of "conservation of total axonal arborizations": Massive compensatory sprouting in the hamster subcortical visual system after early tectal lesions. Experimental Brain Research 1988, 73:505-518.
28. Subang M.C., Richardson P.M. Influence of injury and cytokines on synthesis of monocyte chemoattractant protein-1mRNA in peripheral nervous tissue. European Journal of Neuroscience 2001, 13:521-528.
29. Verge V.M.K., Richardson P.M., Wisenfeld-Hallin Z., et al. Differential influence of nerve growth factor on neuropeptide expression in vivo. Journal of Neuroscience 1995, 15:2081-2096.
30. Taveggia C., Zanazzi G., Petrylak A., et al. Neuregulin-1 type III determines the ensheathment fate of axons. Neuron 2005, 47:681-694.
31. Thomas P.K. Nerve injury. Essays on the Nervous System 1974, 44-70. Clarendon, Oxford. R. Bellairs, E.G. Gray (Eds.).
32. Woolf C.J. Evidence for a central component of post-injury pain sensitivity. Nature 1983, 306:686-688.