Free Access
Issue
Med Sci (Paris)
Volume 19, Number 5, Mai 2003
Page(s) 567 - 574
Section M/S Revues
DOI https://doi.org/10.1051/medsci/2003195567
Published online 15 May 2003
  1. Lipton JA, Ship JA, Larach- Robinson D. Estimated prevalence and distribution of reported orofacial pain in the United States. J Am Dent Assoc 1993; 124: 115–21. [Google Scholar]
  2. Julius D, Basbaum AI. Molecular mechanisms of nociception. Nature 2001; 413: 203–10. [Google Scholar]
  3. Bolay H, Reuter U, Dunn AK, Huang Z, Boas DA, Moskowitz MA. Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model. Nat Neurosci 2002; 8: 136–42. [Google Scholar]
  4. Burstein R. Deconstructing migraine headache into peripheral and central sensitization. Pain 2001; 89: 107–10. [Google Scholar]
  5. Gerard MW. Afferent impulses of the trigeminal nerve. The intramedullary course of the painful thermal and tactile impulses. Arch Neurol Psychiatr 1923; 9: 306–38. [Google Scholar]
  6. Sjöqvist O. Studies on pain conduction in the trigeminal nerve contribution to surgical treatment of facial pain. Acta Psychiatr Scand 1939; 17:1–139. [Google Scholar]
  7. Young RF. Effect of trigeminal tractotomy on dental sensation in humans. J Neurosurg 1982; 56: 812–8. [Google Scholar]
  8. Graham SH, Sharp FR, Dillon W. Intraoral sensation in patient with brain stem lesions: role of the rostral spinal trigeminal nuclei in pons. Neurology 1988; 38: 1529–33. [Google Scholar]
  9. Dallel R, Raboisson P, Woda A, Sessle BJ. Properties of nociceptive and nonnociceptive neurons in trigeminal subnucleus oralis of the rat. Brain Res 1990; 521: 95–106. [Google Scholar]
  10. Dallel R, Duale C, Luccarini P, Molat JL. Stimulusfunction, wind-up and modulation by diffuse noxious inhibitory controls of responses of convergent neurons of the spinal trigeminal nucleus oralis. Eur J Neurosci 1999; 11: 31–40. [Google Scholar]
  11. Pajot J, Pelissier T, Sierralta F, Raboisson P, Dallel R. Differential effects of trigeminal tractotomy on Aδ- and C-fiber-mediated nociceptive responses. Brain Res 2000; 863: 289–92. [Google Scholar]
  12. Raboisson P, Dallel R, Woda A. Responses of neurones in the ventrobasal complex of the thalamus to orofacial noxious stimulation after large trigeminal tractotomy. Exp Brain Res 1989; 77: 569–76. [Google Scholar]
  13. Hu JW, Sessle BJ, Raboisson P, Dallel R, Woda A. Stimulation of craniofacial muscle afferents induces prolonged facilitatory effects in trigeminal nociceptive brain-stem neurones. Pain 1992; 48: 53–60. [Google Scholar]
  14. Hu JW, Woda A, Sessle BJ. Effects of pre-emptive local anaesthesia on tooth pulp deafferentationinduced neuroplastic changes in cat trigeminal brainstem neurones. Arch Oral Biol 1999; 44: 287–93. [Google Scholar]
  15. Dallel R, Duale C, Molat JL. Morphine administered in the substantia gelatinosa of the spinal trigeminal nucleus caudalis inhibits nociceptive activities in the spinal trigeminal nucleus oralis. J Neurosci 1998; 18: 3529–36. [Google Scholar]
  16. Ressot C, Collado V, Molat JL, Dallel R. Strychnine alters response properties of trigeminal nociceptive neurons in the rat. J Neurophysiol 2001; 86: 3069–72. [Google Scholar]
  17. Woda A, Molat JL, Luccarini P. Low doses of NMDA antagonists in superficial laminae of medulla oblongata facilitate windup of convergent neurons. Neuroscience 2001; 107: 317–27. [Google Scholar]
  18. Voisin D, Luccarini P, Chalus M, Dallel R, Besson JM. Substance P receptor activation contributes to the windup of nociceptive neurons of the rat spinal trigeminal nucleus oralis. Society for Neuroscience, 32th annual meeting, Orlando, 2002. Washington DC: Society for Neuroscience, 2002; 28: 452. [Google Scholar]
  19. Dallel R, Ricard O, Raboisson P. Organization of parabrachial projections from the spinal trigeminal nucleus oralis: an anterograde tracing study in the rat. J Comp Neurol 2003 (sous presse). [Google Scholar]
  20. Voisin D, Guy N, Chalus M, Dallel R, Renaud B. Projections of the spinal trigeminal nucleus oralis to the thalamus: a retrograde tracing study in the rat. Society for Neuroscience, 31th annual meeting, San Diego, 2001. Washington DC: Society for Neuroscience, 2001; 27: 1618. [Google Scholar]
  21. Ahissar E, Sosnik R, Haidarliu S. Transformation from temporal to rate coding in a somatosensory thalamocortical pathway. Nature 2000; 406: 302–6. [Google Scholar]
  22. Besson JM, Chaouch A. Peripheral and spinal mechanisms of nociception. Physiol Rev 1987; 67: 67–185. [Google Scholar]
  23. Luccarini P, Cadet R, Duale C, Woda A. Effects of lesions in the trigeminal oralis and caudalis subnuclei on different orofacial nociceptive responses in the rat. Brain Res 1998; 24: 79–85. [Google Scholar]
  24. Voisin D, Chalus M, Doméjean-Orliaguet S, Dallel R, Woda A. Ascending intranuclear connections relaying nociceptive information from the caudal part to the oral part of the spinal trigeminal nucleus in the rat. In: Pain in Europe III: Advances in pain research and therapy. Nice: European Federation of IASP, 2000 : 192. [Google Scholar]
  25. Woda A. Blanc O, Molat JL, Besson JM, Luccarini P. Nmethyl- D-aspartate receptors of substantia gelatinosa medite an inhibitory influence on central sensitization of nociceptive trigeminal neurons. Society for Neuroscience, 31th annual meeting, San Diego, 2001. Washington DC: Society for Neuroscience, 2001; 27: 425. [Google Scholar]
  26. Villanueva L, Nathan PW. Multiple pain pathways. In: Devor M, Rowbotham MC, Wiesendfeld-Hallin Z, eds. Proceedings of the 9th World Congress on Pain. Seattle: IASP Press, 2000 : 371–86. [Google Scholar]
  27. Rainville P. Brain mechanisms of pain affect and pain modulation. Curr Opin Neurobiol 2002; 12: 195–204. [Google Scholar]
  28. Ergenzinger ER, Glasier MM, Hahm JO, Pons TP. Cortically induced thalamic plasticity in the primate somatosensory system. Nat Neurosci 1998; 1: 226–9. [Google Scholar]
  29. Krupa DJ, Ghazanfar AA, Nicolelis MA. Immediate thalamic sensory plasticity depends on corticothalamic feedback. Proc Natl Acad Sci USA 1999; 96: 8200–5. [Google Scholar]
  30. Desbois C, Le Bars D, Villanueva L. Organization of cortical projections to the medullary subnucleus reticularis dorsalis: a retrograde and anterograde tracing study in the rat. J Comp Neurol 1999; 410: 178–96. [Google Scholar]
  31. Bushnell MC, Duncan GH, Dubner R, He LF. Activity of trigeminothalamic neurons in medullary dorsal horn of awake monkeys trained in a thermal discrimination task. J Neurophysiol 1984; 52: 170–87. [Google Scholar]
  32. Dallel R, Voisin D. Towards a pain treatment based on the identification of the pain-generating mechanisms ? Eur Neurol 2001; 45: 126–32. [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.