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Original Article

Light- and Electron-Microscopic Localization of Primary Dental Afferents to Medullary Dorsal Horn (Pars Caudalis)

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Pages 291-307 | Published online: 10 Jul 2009

References

  • Arvidsson J., Gobel S. An HRP study of the central projections of primary trigeminal neurons which innervate tooth pulps in the cat. Brain Res. 1981; 210: 1–16
  • Barron K. D., McGuinness C. M., Misantone L. J., Zanakis M. F., Grafstein B., Murray M. RNA content of normal and axotomized retinal ganglion cells of rat and goldfish. J. Comp. Neurol. 1985; 236: 265–273
  • Blair R. W. Noxious cardiac input onto neurons in medullary reticular formation. Brain Res. 1985; 326: 335–346
  • Broton J. G., Rosenfeld J. P. Effects of trigeminal tractotomy on facial thermal nociception in the rat. Brain Res. 1985; 333: 63–72
  • Brown A. G. The dorsal horn of the spinal cord. Quart. J. Exp. Physiol. 1982; 67: 193–212
  • Bunt A. H., Haschke R. H., Lund R. D., Calkins D. F. Factors affecting retrograde axonal transport of horseradish peroxidase in the visual system. Brain Res. 1976; 102: 152–155
  • Burton H. Somatic sensory properties of caudal bulbar reticular neurons in the cat (Felis domestica). Brain Res. 1968; 11: 357–372
  • Byers M. R. Sensory innervation of periodontal ligament of rat molars consists of unencapsulated ruffini‐like mechanoreceptors and free nerve endings. J. Comp. Neurol. 1985; 231: 500–518
  • Byers M. R., Martin R. F., O'Connor T. A., Dong W. K. Mesencephalic trigeminal sensory axons in cats form unencapsulated Ruffini‐like mechanoreceptors in periodontal ligament but not tooth pulp. Paper presented at the annual meeting of the Society for Neuroscience. Dallas 1985
  • Capra N. F., Anderson K. V., Pride J. B., Jones T. E. Simultaneous demonstration of neuronal somata that innervate the tooth pulp and adjacent periodontal tissues, using two retrogradely transported anatomic markers. Exp. Neurol. 1984; 86: 165–170
  • Darian‐Smith I. The trigeminal system. Handbook of Sensory Physiology, Vol. 2, Somatosensory System, A. Iggo. Springer‐Verlag, Berlin 1973; 271–314
  • Dawson N. J., Hellon R. F., Hubbard J. I. Cell responses evoked by tooth pulp stimulation above the marginal layer of the cat's trigeminal nucleus caudalis. J. Comp. Neurol. 1980; 193: 983–994
  • Gobel S., Binck J. M. Degenerative changes in primary trigeminal axons and in neurons in nucleus caudalis following tooth pulp extirpations in the cat. Brain Res. 1977; 132: 347–354
  • Gobel S., Falls W. M., Humphrey E. Morphology and synaptic connections of ultra‐fine primary axons in lamina 1 of the spinal dorsal horn: Candidates for the terminal axon arbors of primary neurons with unmyelinated (C) axons. J. Neurosci. 1981; 1: 1163–1179
  • Gobel S., Hockfield S. An anatomical analysis of the synaptic circuitry of layers I, II, and III of the trigeminal nucleus caudalis in the cat. Pain in the Trigeminal Region, D. Anderson, B. Matthews. Elsevier/North‐Holland Biomedical Press, Amsterdam 1977; 203–212
  • Gobel S., Purvis M. B. Anatomical studies of the organization of the spinal V nucleus: The deep bundles and the spinal V tract. Brain Res. 1972; 48: 27–44
  • Goldberger M. E., Murray M. Recovery of movement and axonal sprouting may obey some of the same laws. Neuronal Plasticity, C. W. Cotman. Raven Press, New York 1978; 73–96
  • Henry M. A., Westrum L. E., Johnson L. R. Enhanced ultrastructural visualization of the horseradish peroxidase‐tetramethyl benzidine reaction product. J. Histochem. Cytochem. 1985a; 33: 1256–1259
  • Henry M. A., Westrum L. E., Johnson L. R. Ultrastructure of transganglionic HRP transport in cat trigeminal system. Brain Res. 1985b; 334: 255–266
  • Jacquin M. F., Semba K., Egger M. D., Rhoades R. W. Organization of HRP‐labeled trigeminal mandibular primary afferent neurons in the rat. J. Comp. Neurol. 1983; 215: 397–420
  • Jenq C. ‐B., Coggeshall R. E. Regeneration of axons in tributary nerves. Brain Res. 1984; 310: 107–121
  • Johnson L. R., Westrum L. E., Canfield R. C. Ultrastructural study of transganglionic degeneration following dental lesions. Exp. Brain Res. 1983; 52: 226–234
  • Johnson L. R., Westrum L. E., Henry M. A., Canfield R. C. Toxic ricin demonstrates a dual dental projection. Brain Res. 1985; 345: 379–383
  • Jones T. E., Anderson K. V., Capra N. F. Studies on primary and permanant teeth: Common innervation features. Paper presented at the annual meeting of the Society for Neuroscience. Anaheim, CA 1984
  • Kerr F. W. L. The divisional organization of afferent fibres of the trigeminal nerve. Brain 1963; 86: 721–732
  • Kerr F. W. L. The fine structure of the sub‐nucleus caudalis of the trigeminal nerve. Brain Res. 1970; 23: 129–145
  • Kruger L. A critical review of theories concerning the organization of the sensory trigeminal complex of the brainstem. Oral‐Facial Sensory and Motor Mechanisms, K. Dubner, Y. Kawamura. Appleton‐Century‐Crofts, New York 1970; 135–158
  • Light A. R., Perl E. R. Reexamination of the dorsal root projection to the spinal dorsal horn including observations on the differential termination of coarse and fine fibers. J. Comp. Neurol. 1979a; 186: 117–132
  • Light A. R., Perl E. R. Spinal termination of functionally identified primary afferent neurons with slowly conducting myelinated fibers. J. Comp. Neurol. 1979b; 186: 133–150
  • Lindquist T. D., Sturman J. A., Gould R. M., Ingoglia N. A. Axonal transport of polyamines in intact and regenerating axons of the rat sciatic nerve. J. Neurochem. 1985; 44: 1913–1919
  • Lisney S. J. W. Observations on facial nociception in a monkey after destruction of the rostral part of the trigeminal sensory nuclear complex. Pain 1985; 21: 129–135
  • Marfurt C. F. The somatotopic organization of the cat trigeminal ganglion as determined by the horseradish peroxidase technique. Anat. Rec. 1981; 201: 105–118
  • Marfurt C. F., Turner D. F. The central projections of tooth pulp afferent neurons in the rat as determined by the transganglionic transport of the horseradish peroxidase. J. Comp. Neurol. 1984; 223: 535–547
  • Tracing Neural Connections with Horseradish Peroxidase, M. ‐M. Mesulam. IBRO Handbook Series, Wiley, ChichesterEngland 1982
  • Mesulam M. ‐M., Rosene D. L. Sensitivity in horseradish peroxidase neurohistochemistry: A comparative and quantitative study of nine methods. J. Histochem. Cytochem. 1979; 27: 763
  • Ogilvie A. L. Histology of the dental pulp. An Atlas of Pulpal and Periapical Biology, A. L. Ogilvie, J. I. Ingle. Lea & Febiger, Philadelphia 1965; 239–243
  • Perl E. R. Characterization of nociceptors and their activation of neurons in the superficial dorsal horn: First steps for the sensation of pain. Advances in Pain Research and Therapy, L. Kruger, J. C. Liebeskind. Raven Press, New York 1984; Vol. 6: 23–51
  • Rethelyi M., Light A. R., Perl E. R. Synaptic complexes formed by functionally defined primary afferent units with fine myelinated fibers. J. Comp. Neurol. 1982; 207: 381–393
  • Robertson B., Grant G. A comparison between wheat germ agglutinin and choleragenoid‐horseradish peroxidase as anterogradely transported markers in central branches of primary sensory neurones in the rat with some observations in the cat. Neuroscience 1985; 14: 895–905
  • Rulli R. D., Wilson D. L. Proteins in fast axonal transport are differentially transported in branches of sensory nerves. Brain Res. 1985; 335: 165–168
  • Sakumoto T., Nagai T., Kimura H., Maeda T. Electron microscopic visualization of tetramethyl benzidine reaction product on horseradish peroxidase neurohistochemistry. Cell. Mol. Biol. 1980; 26: 211–216
  • Schmidt M. L., Lee Y. M.‐Y., Trojanowski J. Q. Immunochemical detection of diverse molecular species of horseradish peroxidase recovered from rat superior cervical ganglion following retrograde transport. Brain Res. 1985; 328: 65–72
  • Shigenaga Y., Nakatani Z., Nishimori T., Suemune S., Kuroda R., Matano S. The cells of origin of cat trigeminothalamic projections, especially in the caudal medulla. Brain Res. 1983; 277: 201–222
  • Shigenaga Y., Nishimori T., Suemune S., Chen I. C., Nasution I. D., Sato H., Okamoto T., Sera M., Tabuchi K., Kagawa K., Hosoi M. Laminar‐related projection of primary trigeminal fibers in the caudal medulla demonstrated by transganglionic transport of horseradish peroxidase. Brain Res. 1984; 309: 341–345
  • Sjoquist O. Studies on pain conduction in the trigeminal nerve: A contribution to the surgical treatment of facial pain. Acta Psychiat. Scand. 1938; 17: 9–139, Suppl.
  • Steindler D. A. Trigeminocerebellar, trigeminotectal, and trigeminothalamic projections: A double retrograde axonal tracing study in the mouse. J. Comp. Neurol. 1985; 237: 155–175
  • Strassburg M. Morphologic reaction of the trigeminal ganglion after experimental surgery on the maxillodental region. J. Oral. Surg. 1967; 25: 107–114
  • Wesselmann U., McLachlan E. M. The effect of previous transection on quantitative estimates of the preganglionic neurones projecting in the cervical sympathetic trunk of the guinea‐pig and the cat made by retrograde labeling of damaged axons by horseradish peroxidase. Neuroscience 1984; 13: 1299–1309
  • Westrum L. E., Canfield R. C. Normal loss of milk teeth causes degeneration in brain stem. Exp. Neurol. 1979; 65: 169–177
  • Westrum L. E., Canfield R. C., Black R. G. Axonal degeneration patterns in the cat brainstem spinal trigeminal nucleus after tooth pulp removal. Advances in Pain Research and Therapy, J. J. Bonica, D. Albe‐Fessard. Raven Press, New York 1976; Vol. 1: 161–164
  • Westrum L. E., Canfield R. C., O'Connor T. A. Projections from dental structures to the brain stem trigeminal complex as shown by transganglionic transport of horseradish peroxidase. Neurosci. Lett. 1980; 20: 31–36
  • Westrum L. E., Canfield R. C., O'Connor T. A. Each canine tooth projects to all brain stem trigeminal nuclei in cat. Exp. Neurol. 1981; 74: 787–799
  • Westrum L. E., Johnson L. R., Canfield R. C. Ultrastructure of transganglionic degeneration in brain stem trigeminal nuclei during normal primary tooth exfoliation and permanent tooth eruption in the cat. J. Comp. Neurol. 1984; 230: 198–206
  • Yamamoto T., Iwasaki Y., Konno H. Retrograde axoplasmic transport of toxic lectins is useful for transganglionic tracings of the peripheral nerve. Brain. Res. 1983; 274: 325–328

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