Cortical control of tongue protrusion and lateral movements in the cat

References

• Asanuma H, Arissian K. Experiments on functional role of peripheral input to motor cortex during voluntary movements in the monkey. J Neurophysiol 1984; 52: 212–227
   PubMed Web of Science ®Google Scholar
• Fitzgibbon T. Organization of reciprocal connections between the perigeniculate nucleus and dorsal lateral geniculate nucleus in the cat: A transneuronal transport study. Vis Neurosci 2002; 19: 511–520
   PubMedGoogle Scholar
• Hassler R, Muhs-Clement K. Architektonischer Aufbau des Sensomotorischen und parietalen Cortex der Katze. J. Hirnforasch 1964; 6: 377–420
   Google Scholar
• Hiiemae KM. Mammalian mastication: A review of the activity of the jaw muscles and the movements they produce in chewing. Development, function and evolution of teeth, PM Butler, KA Jovsey. Academic Press, London 1978; 359–398
   Google Scholar
• Hikosaka O, Nalahara H, Rand MK, Sakai K, Lu X, Nakamura K, Miyachi S, Doya K. Parallel neural networks for learning sequential procedures. Trends Neurosci 1999; 22: 464–471
   PubMed Web of Science ®Google Scholar
• Hiraba H. Function of the orofacial SI during mastication in awake cats: Changes in masticatory movements and activities of mastication-related neurons in motor cortices following a lesion in the orofacial SI awake cats. Neurobiology and mastication—From molecular to system approach, Y Nakamura, BJ Sessle. Elsevier, Amsterdam 1999; 494–503
   Google Scholar
• Hiraba H. The function of sensory information from the first somatosensory cortex for facial movements during ingestion in cats. Somatosens Mot Res 2004; 21: 87–97
   PubMed Web of Science ®Google Scholar
• Hiraba H, Sato T. Cortical control of mastication in the cat—Properties of mastication-related neurons in motor and masticatory cortices. Somatosens Mot Res 2004; 21: 217–227
   PubMed Web of Science ®Google Scholar
• Hiraba H, Sato T. Cerebral control of face, jaw, and tongue movements in awake cats: Changes in regional cerebral blood flow during lateral feeding. Somatosens Mot Res 2005a; 22: 307–317
   PubMed Web of Science ®Google Scholar
• Hiraba H, Sato T. Cortical control of mastication in cats: Changes in masticatory movements following lesions in the masticatory cortex. Somatosens Mot Res 2005b; 22: 171–181
   PubMed Web of Science ®Google Scholar
• Hiraba H, Sato T. Cortical control of mastication in cats. 2. Deficits of masticatory movements following a lesion in the motor cortex. Somatosens Mot Res 2005c; 22: 183–192
   PubMedGoogle Scholar
• Hiraba H, Sato T, Nakakawa K, Ueda K. Cortical control of appropriate tongue protrusion during licking in cats—Increase in regional cerebral blood flow (rCBF) of the contralateral area P and in tongue protrusion after the unilateral area P lesion. Somatosens Mot Res 2009; 26: 82–89
   PubMed Web of Science ®Google Scholar
• Hiraba H, Sato T, Nakayama E, Yamaoka M, Inoue M, Sato M, Iida T, Wada S, Ueda K. Changes in localization arrangement in the hypoglossal nucleus after the neurectomy of unilateral hypoglossal nerve (medial branch) in cats. Somatosens Mot Res 2010; 27: 93–99
   PubMed Web of Science ®Google Scholar
• Hiraba H, Sato T, Saito K, Iwakami T, Mizoguchi N, Fukano M, Ueda K. Organization of cortical processing for facial movements during licking in cats. Somatosens Mot Res 2007; 24: 115–126
   PubMed Web of Science ®Google Scholar
• Hiraba H, Yamaguchi Y, Iwamura Y. Mastication-related neurons in the orofacial first somatosensory cortex of awake cats. Somatosens Mot Res 1997; 14: 126–137
   PubMed Web of Science ®Google Scholar
• Hiraba H, Yamaguchi Y, Sato H, Ishibashi Y, Iwamura Y. Deficits of masticatory movements caused by lesions in the orofacial somatosensory cortex of the awake cat. Somatosens Mot Res 2000; 17: 361–372
   PubMed Web of Science ®Google Scholar
• Hiraba H, Yoshida T, Yamaguchi Y, Kamogawa H, Oishi T. Neuronal activity in three oro-facial motor cortical areas of conscious cats during mastication. Shika Kiso Igakushi Zasshi 1993; 35: 386–401, (in Japanese)
   Google Scholar
• Hiraba H, Yoshida T, Yamaguchi Y, Oishi T, Fujita S, Kamogawa H, Kondo M. Activity of mastication related neurons in the masticatory cortex of awake cats. Shika Kiso Igakushi Zasshi 1994; 36: 406–419, (in Japanese)
   Google Scholar
• Huppenbauer CB, Tanzer L, Jones KJ. Detection of retrogradely transported WGA-HRP in axotomized adult hamster facial motoneurons occurs after initiation of the axon reaction. J Neurocytol 2001; 30: 907–916
   PubMedGoogle Scholar
• Itoh K, Yasui Y, Takada M, Mitani A, Kaneko T, Sugimoto T, Mizuno N. An anterograde–retrograde transneuronal transport of conjugates of wheat germ agglutinin with horseradish peroxidase (WGA-HRP): Labeling of neurons in the reticular nucleus of the thalamus with WGA-HRP injected into the posterior column nuclei in the cat. Brain Res 1984; 323: 185–187
   PubMedGoogle Scholar
• Iwamura Y. Hierarchical somatosensory processing. Curr Opin Neurobiol 1998; 8: 522–528
   PubMed Web of Science ®Google Scholar
• Iwamura Y. Bilateral receptive field neurons and callosal connections in the somatosensory cortex. Phil Trans R Soc Lond B Biol Sci 2000; 355: 267–274
   PubMedGoogle Scholar
• Mesulam MM. Tetramethyl benzidine for horseradish peroxidase neurohistochemistry: a non-carcinogenic blue reaction product with superior sensetivity for visualizing neural afferents and efferents. J Histochem Cytochem 1978; 26: 106–117
   PubMed Web of Science ®Google Scholar
• Nishimori T, Sera MS, Suemune A, Yoshida K, Tsuru Y, 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
• Shinoda Y, Futami T, Kakei S. Inputs from the cerebellar nuclei to the forelimb area of the motor cortex. Control of arm movement in space, R Caminiti, PB Johnson, Y Burnod. Springer-Verlag, Berlin 1992; 65–84
   Google Scholar
• Yasui Y, Ito K, Mirani A, Takada M, Mizuno N. Cerebral cortex projections to the reticular regions around the trigeminal motor nucleus in the cat. J Comp Neurol 1985a; 241: 348–356
   PubMed Web of Science ®Google Scholar
• Yasui Y, Ito K, Takada M, Mitani A, Kaneko T, Mizuno N. Direct cortical projection in the parabrachial nucleus in the cat. J Comp Neurol 1985b; 234: 77–86
   PubMed Web of Science ®Google Scholar
• Yasui Y, Ito K, Kaneko T, Shigenoto R, Mizuno N. Topographical projection from the cerebral cortex in the nucleus of the solitary tract in cat. Exp Brain Res 1991; 85: 75–84
   PubMed Web of Science ®Google Scholar