Literature DB >> 2707333

Modifications of masticatory behavior after trigeminal deafferentation in the rabbit.

T Inoue1, T Kato, Y Masuda, T Nakamura, Y Kawamura, T Morimoto.   

Abstract

Bilateral trigeminal deafferentation was performed in the rabbit in order to assess the role of orofacial inputs in regulation of the pattern of jaw movements during chewing. After bilateral combined section of the maxillary and inferior alveolar nerves, the animals did not eat food by themselves in the first postoperative week. However, they could chew and swallow when food was inserted into the mouth by an experimenter. The pattern of jaw movements and associated EMG activities of masticatory muscles during chewing were modulated remarkably by deafferentation. These modifications include 1) decrease in the horizontal excursions of the mandible at the power phase, 2) decrease in the maximum gape, 3) insufficient occlusion at the power phase (or increase in the minimum gape), 4) irregular patterns of jaw movements, 5) facilitation of the chewing rate, 6) increase in the number of chewing cycles in a masticatory sequence (the process from acceptance of food to swallowing), and 7) decrease in jaw-closing muscle activities. The findings indicate that deafferentation of the trigeminal sensory branches reduced masticatory force. On the other hand, no significant change was seen in the animals with disruption of cutaneous sensations of the face due to bilateral section of the infraorbital and mental nerves. Intraoral sensations rather than extraoral sensations may thus be important for regulation of masticatory force and jaw movements during chewing. Jaw movements during chewing were also analyzed in the animals with either bilateral ablation of the cortical masticatory area (CMA) or bilateral lesion of the ventral posteromedial nucleus (VPM) of the thalamus in order to examine whether profound effects of trigeminal deafferentation are produced via the transcortical loop. The animals with lesion of either the CMA or VPM demonstrated disturbances in feeding behavior, including the dropping of ingested food from the mouth, elongation of a masticatory process, reduction in the chewing efficiency, etc. However, the pattern of jaw movements during chewing were essentially similar to that in the preoperative period. These results do not necessarily deny a contribution of the CMA to regulation of jaw movements but suggest that the transcortical feedback loop via the CMA and thalamic VPM nucleus would not primarily be responsible for pattern formation of jaw movements during chewing in the rabbit. Probably, the sensory feedback via the transcortical loop may indirectly facilitate activities of the brain stem CPG, which facilitates the chewing rhythm or enables masticatory sequences to be conducted smoothly.

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Year:  1989        PMID: 2707333     DOI: 10.1007/BF00247360

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  41 in total

1.  Trigeminal nerve and eating in the pigeon (Columba livia): neurosensory control of the consummatory responses.

Authors:  H P Zeigler; M Miller
Journal:  J Comp Physiol Psychol       Date:  1975-10

2.  Patterns of mandibular movement and jaw muscle activity during mastication in the monkey.

Authors:  E S Luschei; G M Goodwin
Journal:  J Neurophysiol       Date:  1974-09       Impact factor: 2.714

3.  Characteristics of rhythmic jaw movements of the rabbit.

Authors:  T Morimoto; T Inoue; T Nakamura; Y Kawamura
Journal:  Arch Oral Biol       Date:  1985       Impact factor: 2.633

4.  Corticobulbar projections and orofacial and muscle afferent inputs of neurons in primate sensorimotor cerebral cortex.

Authors:  M A Sirisko; B J Sessle
Journal:  Exp Neurol       Date:  1983-12       Impact factor: 5.330

Review 5.  The reorganization of somatosensory cortex following peripheral nerve damage in adult and developing mammals.

Authors:  J H Kaas; M M Merzenich; H P Killackey
Journal:  Annu Rev Neurosci       Date:  1983       Impact factor: 12.449

6.  Trigeminal deafferentation and ingestive behavior in rats.

Authors:  M G Miller
Journal:  J Comp Physiol Psychol       Date:  1981-04

7.  Evidence for peripheral activation of the trigeminal rhythm generator in the decerebrate rat, obtained by Fourier analysis of conditioning testing curves.

Authors:  A J Thexton; C Griffiths; J McGarrick
Journal:  Arch Oral Biol       Date:  1980       Impact factor: 2.633

8.  Activity of neurons in the lower precentral cortex during voluntary and rhythmical jaw movements in the monkey.

Authors:  J P Lund; Y Lamarre
Journal:  Exp Brain Res       Date:  1974-02-15       Impact factor: 1.972

9.  Reflex and locomotor changes following unilateral deafferentation of rat hind limb assessed by chronic electromyography.

Authors:  P Hník; R Vejsada; S Kasicki
Journal:  Neuroscience       Date:  1981       Impact factor: 3.590

10.  Reinnervation of teeth, mucous membrane and skin following section of the inferior alveolar nerve in the cat.

Authors:  P P Robinson
Journal:  Brain Res       Date:  1981-09-14       Impact factor: 3.252

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  17 in total

1.  Directional sensitivity of human periodontal mechanoreceptive afferents to forces applied to the teeth.

Authors:  M Trulsson; R S Johansson; K A Olsson
Journal:  J Physiol       Date:  1992-02       Impact factor: 5.182

2.  Involvement of histaminergic inputs in the jaw-closing reflex arc.

Authors:  Chikako Gemba; Kiyomi Nakayama; Shiro Nakamura; Ayako Mochizuki; Mitsuko Inoue; Tomio Inoue
Journal:  J Neurophysiol       Date:  2015-04-22       Impact factor: 2.714

3.  Forces applied by the incisors and roles of periodontal afferents during food-holding and -biting tasks.

Authors:  M Trulsson; R S Johansson
Journal:  Exp Brain Res       Date:  1996       Impact factor: 1.972

4.  Involvement of the basal nucleus of Meynert on regional cerebral cortical vasodilation associated with masticatory muscle activity in rats.

Authors:  Harumi Hotta; Harue Suzuki; Tomio Inoue; Mark Stewart
Journal:  J Cereb Blood Flow Metab       Date:  2019-12-17       Impact factor: 6.200

5.  Chewing rates among domestic dog breeds.

Authors:  Geoffrey E Gerstner; Meghan Cooper; Peter Helvie
Journal:  J Exp Biol       Date:  2010-07-01       Impact factor: 3.312

6.  Modification of Masticatory Rhythmicity Leading to the Initiation of the Swallowing Reflex in Humans.

Authors:  Masaki Yoneda; Kazuya Saitoh
Journal:  Dysphagia       Date:  2017-11-02       Impact factor: 3.438

7.  Different corticostriatal projections from two parts of the cortical masticatory area in the rabbit.

Authors:  Yuji Masuda; Seo Kwan Kim; Takafumi Kato; Seiji Iida; Atsushi Yoshida; Yoshihisa Tachibana; Toshifumi Morimoto
Journal:  Exp Brain Res       Date:  2004-10-21       Impact factor: 1.972

8.  Differential mastication kinematics of the rabbit in response to food and water: implications for conditioned movement.

Authors:  Keith D Huff; Yukiko Asaka; Amy L Griffin; William P Berg; Matthew A Seager; Stephen D Berry
Journal:  Integr Physiol Behav Sci       Date:  2004 Jan-Mar

Review 9.  How the brainstem controls orofacial behaviors comprised of rhythmic actions.

Authors:  Jeffrey D Moore; David Kleinfeld; Fan Wang
Journal:  Trends Neurosci       Date:  2014-06-02       Impact factor: 13.837

10.  Functional analysis of the rabbit temporomandibular joint using dynamic biplane imaging.

Authors:  Sarah E Henderson; Riddhi Desai; Scott Tashman; Alejandro J Almarza
Journal:  J Biomech       Date:  2014-02-18       Impact factor: 2.712

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