The Dorsomedial Portion of Trigeminal Nucleus Oralis (Vo) in the Rat: Cytology and Projections to the Cerebellum

References

• Armstrong D. M., Campbell N. C., Edgley S. A., Schild R. F., Trott J. R. Investigations of the olivocerebellar and spino‐olivary pathways. The Cerebellum—New Vistas, S. L. Palay, V. Chan‐Palay. Springer‐Verlag, New York 1982; 194–232
   Google Scholar
• 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; 10: 1–16
   Google Scholar
• Azerad J., Woda A., Albe‐Fessard D. Physiological properties of neurons in different parts of the cat trigeminal sensory complex. Brain Res. 1982; 246: 7–21
   PubMed Web of Science ®Google Scholar
• Bower J. M., Beerman D. H., Gibson J. M., Shambes G. M., Welker W. Principles of organization of a cerebro‐cerebellar circuit: Micromapping projections from cerebral (SI) to cerebellar (granule cell) tactile areas of rats. Brain Behav. Evol. 1981; 18: 1–18
   Google Scholar
• Brown P. A. The inferior olivary connections to the cerebellum in the rat studied by the retrograde axonal transport of horseradish peroxidase. Brain Res. Bull. 1980; 5: 267–275
   Google Scholar
• Conde F., Conde H. Étude de la morphologie des cellules du noyeau rouge du chat par la methode de Golgi‐Cox. Brain Res. 1973; 53: 249–271
   Google Scholar
• Darian‐Smith D., Mayday G. Soma‐totopic organization within the brainstem trigeminal complex of the cat. Exp. Neurol. 1960; 2: 290–309
   PubMed Web of Science ®Google Scholar
• Erzurumlu R. S., Bates C. A., Killac‐key H. P. Differential organization of thalamic projection cells in the brain stem trigeminal complex of the rat. Brain Res. 1980; 198: 427–433
   Google Scholar
• Falls W. M. A Golgi type II neuron in trigeminal nucleus oralis: A Golgi study in the rat. Neurosci. Lett. 1983; 41: 1–1
   PubMed Web of Science ®Google Scholar
• Falls W. M. Termination in trigeminal nucleus oralis of ascending intratrigeminal axons originating from neurons in the medullary dorsal horn: An HRP study in the rat employing light and electron microscopy. Brain Res. 1984a; 290: 136–140
   PubMed Web of Science ®Google Scholar
• Falls W. M. The morphology of neurons in trigeminal nucleus oralis projecting to the medullary dorsal horn (trigeminal nucleus caudalis): A retrograde HRP and Golgi study. Neuroscience 1984b; 13: 1279–1298
   PubMed Web of Science ®Google Scholar
• Falls W. M. Axonal endings terminating on dendrites of identified large trigeminospinal projection neurons in rat trigeminal nucleus oralis. Brain Res. 1984c; 324: 335–341
   PubMed Web of Science ®Google Scholar
• Falls W. M., VanWagner J. P. Orofacial projections to cerebellar tactile areas from the rat spinal trigeminal nucleus. Anat. Rec. 1984; 208: 54A
   Google Scholar
• Falls W. M., Race D. L. Endings of primary trigeminal axons synapsing on dendrites of identified trigeminocerebellar projection neurons in rat trigeminal nucleus oralis, in preparation
   Google Scholar
• Fukushima T., Kerr F. W. L. Organization of trigeminothalamic tracts and other thalamic afferent systems of the brainstem in rat: presence of gelatinosa neurons with thalamic connections. J. Comp. Neurol. 1979; 183: 169–184
   PubMed Web of Science ®Google Scholar
• Gobel S. Golgi studies of the neurons in layer I of the dorsal horn of the medulla (trigeminal nucleus caudalis). J. Comp. Neurol. 1978; 180: 375–394
   PubMedGoogle Scholar
• 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
   PubMed Web of Science ®Google Scholar
• Grant G., Arvidsson J. Transganglionic degeneration in trigeminal primary sensory neurons. Brain Res. 1975; 95: 265–279
   PubMed Web of Science ®Google Scholar
• Huerta M. F., Frankfurter A., Harding J. K. Studies of the principal sensory and spinal trigeminal nuclei of the rat: Projections to the superior colliculus, inferior olive and cerebellum. J. Comp. Neurol. 1983; 220: 147–167
   PubMed Web of Science ®Google Scholar
• Ikeda M. Projections from the spinal and the principal sensory nuclei of the trigeminal nerve to the cerebellar cortex in the cat, as studied by retrograde transport of horseradish peroxidase. J. Comp. Neurol. 1979; 184: 567–586
   PubMed Web of Science ®Google Scholar
• Jacquin M. F., Semba K., Egger M. D., Rhoades R. W. Organization of HRP‐labeled trigeminal primary afferent neurons in the rat. J. Comp. Neurol. 1983; 215: 397–420
   PubMed Web of Science ®Google Scholar
• Joseph J. W., Shambes G. M., Gibson J. M., Welker W. Tactile projections to granule cells in caudal vermis of the rat's cerebellum. Brain Behav. Evol. 1978; 15: 141–149
   PubMed Web of Science ®Google Scholar
• Kassel J. Superior colliculus projections to tactile areas of rat cerebellar hemispheres. Brain Res. 1980; 202: 291–305
   Google Scholar
• Kerr F. W. L. The divisional organization of afferent fibers of the trigeminal nerve. Brain 1963; 86: 721–732
   PubMed Web of Science ®Google Scholar
• Killackey H. P., Erzurumlu R. S. Trigeminal projections to the superior colliculus of the rat. J. Comp. Neurol. 1981; 201: 221–242
   Google Scholar
• Marfurt C. F. The central projections of trigeminal primary afferent neurons in the cat as determined by the transganglionic transport of horseradish peroxidase. J. Comp. Neurol. 1981; 203: 785–798
   PubMed Web of Science ®Google Scholar
• Marfurt C. F., Turner D. F. The central projections of tooth pulp afferent neurons in the rat as determined by the transganglionic transport of horseradish peroxidase. J. Comp. Neurol. 1984; 223: 535–547
   PubMed Web of Science ®Google Scholar
• Matsushita M., Ikeda M., Okado N. The cells of origin of the trigeminothalamic, trigeminospinal and trigeminocerebellar projections in the cat. Neuroscience 1982; 7: 1439–1454
   PubMed Web of Science ®Google Scholar
• Mesulam M. ‐M. Tetramethylbenzidine 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
• Panneton W. M., Burton H. Corneal and periocular representation within the trigeminal sensory complex in the cat studied with transganglionic transport of horseradish peroxidase. J. Comp. Neurol. 1981; 199: 327–344
   PubMedGoogle Scholar
• Patrick G. W., Haines D. E. Cerebellar afferents to paramedian lobule from the trigeminal complex in Tupaia glis: A horseradish peroxidase (HRP) study. J. Morphol. 1982; 772: 209–222
   Google Scholar
• Ramón y Cajal S. Histologic du Système Nerveux de l'Homme et des Vertébrés. Institute Ramón y Cajal, Madrid 1911; Vol. 1
   Google Scholar
• Ruggiero D. A., Ross C. A., Reis D. J. Projections from the spinal trigeminal nucleus to the entire length of the spinal cord in the rat. Brain Res. 1981; 225: 225–233
   PubMed Web of Science ®Google Scholar
• Saigal R. P., Karamanlidis A. N., Voogd J., Managana O., Michaloudi H. Secondary trigeminocerebellar projections in sheep studied with the horseradish peroxidase tracing method. J. Comp. Neurol. 1980; 189: 537–553
   Google Scholar
• Sessle B. J., Greenwood L. F. Inputs to trigeminal brain stem neurons from facial, oral, tooth pulp and pharyngolaryngeal tissues: Responses to innocuous and noxious stimuli. Brain Res. 1976; 117: 211–226
   PubMed Web of Science ®Google Scholar
• Shambes G. M., Beerman D. H., Welker W. Multiple tactile areas in cerebellar cortex: another patchy cutaneous projection to granule cell columns in rats. Brain Res. 1978; 157: 123–128
   PubMed Web of Science ®Google Scholar
• Shambes G. M., Gibson J. M., Welker W. Fractured somatotopy in granule cell tactile areas of rat cerebellar hemispheres revealed by micromapping. Brain Behav. Evol. 1978b; 15: 94–140
   PubMed Web of Science ®Google Scholar
• Silverman J. D., Kruger L. Bifurcating projections of the rat sensory trigeminal complex revealed by fluorescent dye retrograde transport. Anat. Rec. 1983; 205: 184A
   Google Scholar
• Somana R., Kotchabhakdi N., Walberg F. Cerebellar afferents from the trigeminal sensory nuclei in the cat. Exp. Brain Res. 1980; 38: 57–64
   Google Scholar
• Steindler D. A. Trigemino‐cerebellar projections in normal and reeler mutant mice. Neurosci. Lett. 1977; 6: 293–300
   Google Scholar
• Watson C. R. R., Switzer R. C., III. Trigeminal projections to cerebellar tactile areas in the rat—origin mainly from n. interpolaris and n. principalis. Neurosci. Lett. 1978; 10: 77–82
   PubMed Web of Science ®Google Scholar
• Woolston D. C., Kassel J., Gibson J. M. Trigeminocerebellar mossy fiber branching to granule cell layer patches in the rat cerebellum. Brain Res. 1981; 209: 255–269
   PubMed Web of Science ®Google Scholar