Article Data

  • Views 268
  • Dowloads 53

Original Research

Open Access

Future Basic Science Directions Into Mechanisms of Neuropathic Pain

  • James L. Henry1,*,

1Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada

DOI: 10.11607/jofph.18306 Vol.18,Issue 4,December 2004 pp.306-310

Published: 30 December 2004

*Corresponding Author(s): James L. Henry E-mail: james.henry@fmd.uwo.ca

Abstract

The aim of this article is to outline mechanisms underlying genera-tion and maintenance of pain arising from trauma to peripheral nerve fibers and to present an overview of our recent studies of animal models of peripheral neuropathic pain and pain of tem-poromandibular disorders (TMD). The former model was induced by placing a polyethylene cuff around the sciatic nerve of the Sprague-Dawley rat and the TMD model was induced by injection of complete Freund’s adjuvant into the rat’s temporomandibular joint. In cuff-implanted rats, ongoing activity of dorsal horn neu-rons was greater than in controls, the cutaneous receptive field size of the neurons was greater, and both noxious and innocuous mechanical stimuli to the receptive field elicited an excitatory response during stimulation but also a marked afterdischarge that lasted up to 30 minutes; this afterdischarge was never observed in control rats in response to innocuous stimulation. The model of TMD was characterized by joint space narrowing, bone remodel-ing, infiltration of immune cells, loss in the range of jaw opening, and signs of nociception. Alterations in the neural substrate of nociception in animal models, and therefore also possibly in humans, appear to include changes in peripheral as well as central neurons. In the periphery, changes include alterations in the phe-notype and central projections of large-diameter sensory nerve fibers. At the level of the trigeminal brainstem and spinal cord, there appear to be several types of change. One type is an increased efficacy of synaptic transmission onto second-order neu-rons. Another type of change is a reduction in inhibitory mecha-nisms, including a shift of gamma-amino butyric acid (GABAA) receptor activation to excitation. There is a need for further stud-ies to focus on mechanisms for either the generation or the mainte-nance, or both, of neuropathic pain.

Keywords

animal models; neuropathic pain; temporomandibular disorders; trigeminal pain

Cite and Share

James L. Henry. Future Basic Science Directions Into Mechanisms of Neuropathic Pain. Journal of Oral & Facial Pain and Headache. 2004. 18(4);306-310.

References

1. Bennett G. Neuropathic pain in the orofacial region: Clinical and research challenges. J Orofac Pain 2004;18: 281–286.

2. Dubner R, Ren K. Brainstem mechanisms of persistent pain following injury. J Orofac Pain 2004;18:299–305.

3. Iwata K, Tsuboi Y, Shima A, et al. Central neuronal changes after nerve injury: Neuroplastic influences of injury and aging. J Orofac Pain 2004;18:293–298.

4. Robinson PP, Boissonade FM, Loescher AR, et al. Peripheral mechanisms for the initiation of pain following trigeminal nerve injury. J Orofac Pain 2004;18:287–292.

5. Bennett GJ, Xie YK. A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man. Pain 1988;33:87–107.

6. Seltzer Z, Dubner R, Shir Y. A novel behavioral model of neuropathic pain disorders produced in rats by partial sciatic nerve injury. Pain 1990;43:205–218.

7. Kim SH, Chung JM. An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat. Pain 1992;50:355–363.

8. Mosconi T, Kruger L. Fixed-diameter polyethylene cuffs applied to the rat sciatic nerve induce a painful neuropathy: Ultrastructural morphometric analysis of axonal alterations. Pain 1996;64:37–57.

9. Luo ZD (ed). Pain Research Methods and Protocols. In: Methods in Molecular Medicine. Totowa, NJ: Humana Press, 2004.

10. Pitcher GM, Ritchie J, Henry JL. Nerve constriction in the rat: Model of neuropathic, surgical, and central pain. Pain 1999;83:37–46.

11. Pitcher GM, Henry JL. Cellular mechanisms of hyperalgesia and spontaneous pain in a spinalized rat model of peripheral neuropathy: Changes in myelinated afferent inputs implicated. Eur J Neurosci 2000;12:2006–2020.

12. Pitcher GM, Henry JL. Nociceptive response to innocuous mechanical stimulation is mediated via myelinated afferents and NK-1 receptor activation in a rat model of neuropathic pain. Exp Neurol 2004;186:173–197.

13. Pitcher GM, Henry JL. Second phase of formalin-induced excitation of spinal dorsal horn neurons in spinalized rats is reversed by sciatic nerve block. Eur J Neurosci 2002;15: 1509–1515.

14. Henry, JL, Couture R, Cuello AC, Pelletier G, Quirion R, Regoli D (eds). Substance P and Neurokinins [Proceedings of Substance P and Neurokinins—Montreal ‘86: A satellite symposium of the XXX International Congress of the International Union of Physiological Sciences]. New York: Springer-Verlag, 1987.

15. Spina E, Perugi G. Antiepileptic drugs: Indications other than epilepsy. Epileptic Disord 2004;6:57–75.

16. Rogawski MA, Loscher W. The neurobiology of antiepileptic drugs for the treatment of nonepileptic conditions. Nature Med 2004;10:685–692.

17. Watson CPN. Management issues of neuropathic trigeminal pain from a medical perspective. J Orofac Pain 2004; 18:366–373.

18. Sotgiu ML, Biella G. Contribution of central sensitization to the pain-related abnormal activity in neuropathic rats. Somatosens Mot Res 2000;17:32–38.

19. Rygh LJ, Kontinen VK, Suzuki R, Dickenson AH. Different increase in C-fiber evoked responses after nociceptive conditioning stimulation in sham-operated and neuropathic rats. Neurosci Lett 2000;288:99–102.

20. Croul S, Radzievsky A, Sverstiuk A, Murray M. NK1, NMDA, 5HT1a, and 5HT2 receptor binding sites in the rat lumbar spinal cord: Modulation following sciatic nerve crush. Exp Neurol 1998;154:66–79.

21. Eaton MJ, Plunkett JA, Karmally S, Martinez MA, Montanez K. Changes in GAD- and GABA-immunoreactivity in the spinal dorsal horn after peripheral nerve injury and promotion of recovery by lumbar transplant of immortalized serotonergic precursors. J Chem Neuroanat 1998;16:57–72.

22. Ibuki T, Hama AT, Wang XT, Pappas GD, Sagen J. Loss of GABA-immunoreactivity in the spinal dorsal horn of rats with peripheral nerve injury and promotion of recovery by adrenal medullary grafts. Neuroscience 1997;76:845–858.

23. Simpson RK Jr, Huang W. Glycine receptor reduction within segmental gray matter in a rat model of neuropathic pain. Neurol Res 1998;20:161–168.

24. Castro-Lopez JM, Malcangio M, Pan BH, Bowery NG. Complex changes of GABAA and GABAB receptor binding in the spinal cord dorsal horn following peripheral inflam-mation or neurectomy. Brain Res 1995;679:289–297.

25. Satoh O, Omote K. Roles of monoaminergic, glycinergic and GABAergic inhibitory systems in the spinal cord in rats with peripheral mononeuropathy. Brain Res 1996; 728:27–36.

26. Coull JAM, Boudreau D, Backhand K, et al. Trans-synaptic shift in anion gradient in spinal lamina I neurons as a mechanism of neuropathic pain. Nature 2003;424:938–942.

27. Stamm T, Hohoff A, Van Meegan A, Meyer U. On the three-dimensional physiological position of the temporo-mandibular joint. J Orofac Orthop 2004;65:280–289.

28. Monje F, Delgado E, Navarro MJ, Miralles C, Alonso del Hoyo JR. Changes in temporomandibular joint after mandibular subcondylar osteotomy: An experimental study in rats. J Oral Maxillofac Surg 1993;51:1221–1234.

29. Lekkas C, Honee GL, van den Hooff A. Effects of experi-mental defects of the articular disc of the temporomandibular joint in rats. J Oral Rehabil 1988;15:141–148.

30. Luz JG, Jaeger RG, de Araujo VC, de Rezende JR. The effect of indirect trauma on the rat temporomandibular joint. Int J Oral Maxillofac Surg 1991;20:48–52.

31. Muto T, Shigeo K, Kanazawa M, Irie K, Yajima T, Kaku T. Ultrastructural study of synovitis induced by trauma to the rat temporomandibular joint (TMJ). J Oral Pathol Med 2003;32:25–33.

32. Harper RP, Kerins CA, McIntosh JE, Spears R, Bellinger LL. Modulation of the inflammatory response in the rat TMJ with increasing doses of complete Freund’s adjuvant. Osteoarthritis Cartilage 2001;9:619–624.

33. Kerins CA, Carlson DS, McIntosh JE, Bellinger LL. Meal pattern changes associated with temporomandibular joint inflammation/pain in rats; analgesic effects. Pharmacol Biochem Behav 2003;75:181–189.

34. Hutchins B, Spears R, Hinton RJ, Harper RP. Calcitonin gene-related peptide and substance P immunoreactivity in rat trigeminal ganglia and brainstem following adjuvant-induced inflammation of the temporomandibular joint. Arch Oral Biol 2000;45:335–345.

35. Zhou Q, Imbe H, Dubner R, Ren K. Persistent Fos protein expression after orofacial deep or cutaneous tissue inflammation in rats: Implications for persistent orofacial pain. J Comp Neurol 1999;412:276–291.

36. Shinoda M, Honda T, Ozaki N, et al. Nerve terminals extend into the temporomandibular joint of adjuvant arthritic rats. Eur J Pain 2003;7:493–505.

37. McLeod AL, Julien J-P, Cuello AC, Krause JE, Ribeiro-da-Silva A. Ectopic substance P-immunoreactive boutons are preferentially presynaptic to neurokinin-1 receptor immunoreactive dendrites in the spinal white matter of transgenic mice. Brain Res 1999;836:1–8.

38. Pitcher GM, Yashpal K, Coderre TJ, Henry JL. Mechanisms underlying antinociception provoked by heterosegmental noxious stimulation in the rat tail-flick test. Neurosci 1995;65:273–281.

39. Romita VVR, Henry JL. Spinal µ-, δ- and κ-opiate receptors mediate intense stimulation-elicited inhibition of a nocicep-tive reflex in the rat. Eur J Pharmacol 1998;357:127–138.

Abstracted / indexed in

Science Citation Index (SCI)

Science Citation Index Expanded (SCIE)

BIOSIS Previews

Scopus

Cumulative Index to Nursing and Allied Health Literature (CINAHL)

Submission Turnaround Time

Conferences

Top