Physiological Identification of Jaw-Movement-Related Neurons in the Trigeminal Nucleus of Cats

References

• Albe-Fessard D., Berkley K. J., Kruger L. J., Ralston H. J., Willis W. D. Diencephalic mechanisms of pain sensation. Brain Res. Rev. 1985; 9: 217–296
   Google Scholar
• Amano N., Hu J. W., Sessle B. J. Responses of neurons in feline trigeminal subnucleus caudalis (medullary dorsal horn) to cutaneous, intraoral, and muscle afferent stimuli. J. Neurophysiol. 1986; 55: 227–243
   PubMed Web of Science ®Google Scholar
• Appenteng K., Donga R., Williams R. G. Morphological and electrophysiological determination of the projections of jaw elevator muscle spindle afferents in rats. J. Physiol. (Lond.) 1985; 369: 93–119
   Google Scholar
• Appenteng K., Lund J. P., Seguin J. J. Behavior of cutaneous mechanoreceptors recorded in mandibular division of gasserian ganglion of the rabbit during movements of lower jaw. J. Neurophysiol. 1982; 47(2)152–166
   Google Scholar
• Arvidsson J., Raappana P. An HRP study of the central projections from primary sensory neurons innervating the rat masseter muscle. Brain Res. 1989; 480: 111–118
   Google Scholar
• Berman A. L. The Brain Stem of the Cat: A Cytoarchitectonic Atlas with Stereotaxic Coordinates. University of Wisconsin Press, Madison 1968
   Google Scholar
• Burgess P. R. Equilibrium points and sensory templates. Behav. Brain Sci. 1992; 15: 720–722
   Google Scholar
• Byrd K. E. Opto-electronic analyses of masticatory mandibular movements and velocities in the rat. Arch. Oral Biol. 1988; 33: 209–215
   Google Scholar
• Capra N. F., Anderson K. V. Responses, properties of, and central projections to subnucleus oralis kinesthetic neurons. J. Dent. Res. 1985; 64: 284
   Google Scholar
• Capra N. F., Dessem D. Central connections of trigeminal primary afferent neurons: Topographical and functional considerations. CRC Crit. Rev. Oral Biol. Med. 1992; 4: 1–52
   PubMedGoogle Scholar
• Capra N. F., Wax T. D. Distribution and central projections of primary afferent neurons that innervate the masseter muscle and mandibular periodontium: A double label study. J. Comp. Neurol. 1989; 279: 341–352
   PubMed Web of Science ®Google Scholar
• Clark F. J. Role of intramuscular receptors in the awareness of limb position. J. Neurophysiol. 1985; 54: 1529–1540
   PubMed Web of Science ®Google Scholar
• Clark F. J., Grigg P., Chapin J. W. The contribution of articular receptors to proprioception with the fingers in humans. J. Neurophysiol. 1989; 61: 186–193
   Google Scholar
• Dessem D., Taylor A. Morphology of jaw-muscle spindle afferents in the rat. J. Comp. Neurol. 1989; 282: 389–403
   PubMed Web of Science ®Google Scholar
• Edin B. B., Abbs J. H. Finger movement responses of cutaneous mechanoreceptors in the dorsal skin of the human hand. J. Neurophysiol. 1991; 65: 657–670
   PubMed Web of Science ®Google Scholar
• Eisenman J., Landgren S., Novin D. Functional organization in the main sensory trigeminal nucleus and in the rostral subdivision of the nucleus of the spinal trigeminal tract in the cat. Acta Physiol. Scand. 1963; 59(Suppl. 214)5–44
   Google Scholar
• Fuller J. H., Schlag J. D. Determination of antidromic excitation by the collision test: Problems of interpretation. Brain Res. 1976; 112: 283–298
   PubMed Web of Science ®Google Scholar
• Gandevia S. C., Burke D. Does the nervous system depend on kinesthetic information to control natural limb movement?. Behav. Brain Sci. 1992; 15: 614–632
   Web of Science ®Google Scholar
• Goodwin G. M., McCloskey D. I., Matthews P. B. C. The contribution of muscle afferents to kinaesthesia shown by vibration induced illusions of movement and the effects of paralyzing joint afferents. Brain 1972a; 95: 705–748
   PubMed Web of Science ®Google Scholar
• Goodwin G. M., McCloskey D. I., Matthews P. B. C. The persistence of appreciable kinesthesia after paralyzing joint afferents but preserving muscle afferents. Brain Res. 1972b; 37: 326–329
   PubMed Web of Science ®Google Scholar
• Goodwin G. M., McCloskey D. I., Matthews P. B. C. Proprioceptive illusions induced by muscle vibration: Contribution by muscle spindles to perception. Science 1972c; 175: 1382–1384
   PubMed Web of Science ®Google Scholar
• Gorniak G. C., Gans C. Quantitative assay of electromyograms during mastication in domestic cats (Felis catus). J. Morphol. 1977; 163: 253–281
   Google Scholar
• Hayward L., Wesselman U., Rymer W. Z. Effects of muscle fatigue on mechanically sensitive afferents of slow conduction velocity in the cat triceps surae. J. Neurophysiol. 1991; 65: 360–370
   PubMed Web of Science ®Google Scholar
• Hayashi H., Sumino R., Sessle B. J. Functional organization of trigeminal subnucleus interpolaris: Nociceptive and innocuous afferent inputs, projections to thalamus, cerebellum, and spinal cord, and descending modulation from periaqueductal gray. J. Neurophysiol. 1984; 51: 890–905
   PubMed Web of Science ®Google Scholar
• Hu J. W., Dostrovsky J. O., Sessle B. J. Functional properties of neurons in cat trigeminal subnucleus caudalis (medullary dorsal horn): I. Responses to oral-facial noxious and nonnoxious stimuli and projections to thalamus and subnucleus oralis. J. Neurophysiol. 1981; 45: 173–192
   Google Scholar
• Hu J. W., Sessle B. J. Comparison of responses of cutaneous nociceptive and nonnociceptive brain stem neurons in trigeminal sub-nucleus caudalis (medullary dorsal horn) and subnucleus oralis to natural and electrical stimulation of the tooth pulp. J. Neurophysiol. 1984; 52: 39–53
   PubMed Web of Science ®Google Scholar
• Kawamura Y., Abe K. Role of sensory information from temporomandibular joint. Bull. Tokyo Med. Dent. Univ. 1974; 27(Suppl)78–82
   Google Scholar
• Lund J. P., Matthews B. Responses of temporomandibular joint afferents recorded in the gasserian ganglion of the rabbit to passive movements of the mandible. Oral-Facial Sensory and Motor Functions, Y. Kawamura, R. Dubner. Quintessence, Tokyo 1981; 153–160
   Google Scholar
• Luo P. F., Li J. The morphology and synaptic forms of thalamic projecting neurons in the trigeminal proprioceptive relay station of the rat. J. Med. Coll. PLA 1992; 4: 361–368
   Google Scholar
• Luschei E. S. Central projections of the mesencephalic nucleus of the fifth nerve: An autoradiographic study. J. Comp. Neurol. 1987; 263: 137–145
   Google Scholar
• Luschei E. S., Goldberg L. J. Neural mechanisms of mandibular control: Mastication and voluntary biting. Handbook of Physiology, Section II, The Nervous System, Part 2, Motor Control, V. B. Brooks. Williams and Wilkins, Baltimore 1981; 1237–1274
   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
• McCloskey D. I. Kinesthetic sensibility. Physiol. Rev. 1978; 58: 763–820
   PubMed Web of Science ®Google Scholar
• Mense S. Slowly conducting afferent fibers from deep tissues—neurobiological properties and central nervous actions. Progress in Sensory Physiology, D. Ottoson. Springer-Verlag, Berlin 1986; Vol. 6: 139–219
   Google Scholar
• Millar J. Convergence of joint cutaneous and muscle afferents onto cuneate neurones in the cat. Brain Res. 1979; 175: 347–350
   Google Scholar
• Miyazaki R., Luschei E. S. Responses of neurons in nucleus supratrigeminalis to sinusoidal jaw movements in the cat. Exp. Neurol. 1987; 96: 145–157
   PubMed Web of Science ®Google Scholar
• Mizuno N., Sauerland E. K. Trigeminal proprioceptive projections to the hypoglossal nucleus and the cervical gray column. J. Comp. Neurol. 1970; 139: 215–221
   Google Scholar
• Mizuno N., Yasui Y., Nomura S., Itoh K., Konishi A., Takada M., Kudo M. A light and electron microscopic study of premotor neurons for the trigeminal motor nucleus. J. Comp. Neurol. 1983; 215: 290–298
   PubMedGoogle Scholar
• Morimoto T., Inoue H., Kawamura Y. Diameter spectra of sensory and motor fibers in nerves to jaw closing and jaw opening muscles in the cat. Japan. J. Physiol. 1982; 32: 171–182
   Google Scholar
• Nishimori T., Sera M., Suemune S., Yoshida A., Tsura K., Tsuiki Y., Akisaka T., Okamoto T., Dateoka Y., Shigenaga Y. The distribution of muscle primary afferents from the masseter nerve to the trigeminal sensory nuclei. Brain Res. 1986; 372: 375–381
   PubMedGoogle Scholar
• Nomura S., Mizuno N. Differential distribution of cell bodies and central axons of mesencephalic nucleus neurons supplying the jaw-closing muscles and periodontal tissue: A transganglionic study in the cat. Brain Res. 1985; 359: 311–319
   Google Scholar
• Olsson K. Å, Westberg K. G. Integration in trigeminal premotor interneurones in the cat: 2. Functional characteristics of neurones in the subnucleus-gamma of the oral nucleus of the spinal trigeminal tract with a projection to the digastric motoneurone subnucleus. Exp. Brain Res. 1991; 84: 115–124
   Google Scholar
• Ostapoff E. M., Johnson J. I., Albright B. C. Medullary sources of projections to the kinesthetic thalamus in raccoons: External and basal cuneate nuclei and cell groups x and z. J. Comp. Neurol. 1987; 267: 231–252
   Google Scholar
• Paintal A. S. Functional analysis of group III afferent fibers of mammalian muscle. J. Physiol. (Lond.) 1960; 152: 250–270
   Google Scholar
• Raappana P., Arvidsson J. Location, morphology, and central projections of mesencephalic trigeminal neurons innervating rat masticatory muscles studied by axonal transport of choleragenoid—horseradish peroxidase. J. Comp. Neurol. 1993; 32: 103–114
   Google Scholar
• Ro J. Y., Capra N. F., Donga R. Receptive field properties of ipsilateral trigeminothalamic neurons in cats. Soc. Neurosci. Abstr. 1992; 18: 747
   Google Scholar
• Ruggerio D. A., Ross C. A., Kumada M., Reis D. J. Reevaluations of projections from the mesencephalic trigeminal nucleus to the medulla and spinal cord: New projections, a combined retrograde and anterograde horseradish peroxidase study. J. Comp. Neurol. 1982; 206: 278–292
   Google Scholar
• Sessle B. J., Hu J. W., Amano N., Zhong G. Convergence of cutaneous, tooth pulp, visceral, neck and muscle afferents onto nociceptive and non-nociceptive neurones in trigeminal subnucleus caudalis (medullary dorsal horn) and its implications for referred pain. Pain 1986; 27: 219–235
   PubMed Web of Science ®Google Scholar
• Shigenaga Y., Mitsuhko Y., Shirana Y., Tsuru H. Two types of jaw muscle spindle afferents in the cat as demonstrated by intraaxonal staining with HRP. Brain Res. 1990; 514: 219–237
   PubMed Web of Science ®Google Scholar
• Shigenaga Y., Sera M., Nishimori T., Suemune S., Nishimura M., Yoshida A., Tsuru K. The central projections of masticatory afferent fibers to the trigeminal sensory nuclear complex and upper cervical spinal cord. J. Comp. Neurol. 1988; 268: 489–507
   PubMed Web of Science ®Google Scholar
• Weisendanger M., Miles T. S. Ascending pathway of low-threshold muscle afferents to the cerebral cortex and its possible role in motor control. Physiol. Rev. 1982; 62: 1234–1270
   Google Scholar
• Westberg K. G. K., Olsson Å. Integration in trigeminal premotor interneurones in the cat: 1. Functional characteristics of neurones in the subnucleus-gamma of the oral nucleus of the spinal trigeminal tract. Exp. Brain Res. 1991; 84: 102–114
   Google Scholar