Literature DB >> 8459287

Coordination of cortically induced rhythmic jaw and tongue movements in the rabbit.

Z J Liu1, Y Masuda, T Inoue, H Fuchihata, A Sumida, K Takada, T Morimoto.   

Abstract

1. Rhythmic movements of the jaw, tongue, and hyoid that were induced by stimulation of the cortical masticatory area (CMA) were recorded cineradiographically in the anesthetized rabbit. Jaw movements were also recorded by a laser position detector. 2. The evoked jaw movements were classified into four types: small circular (type A), large circular (type B), large vertical (type C), and crescent-shaped (type D). Among these, types B and D resembled the jaw movements of the food transport cycle and those of the chewing cycle in a masticatory sequence. 3. Each type of jaw movement was associated with a particular pattern of tongue and hyoid movements. In general, the tongue protruded during jaw opening and retracted during jaw closure. The hyoid generally moved upward and forward during jaw opening but downward and backward during jaw closure. 4. Electromyograms (EMGs) were recorded from jaw muscles [masseter (Ma) and digastric (Di) muscles], extrinsic tongue muscles [styloglossus (Sg) and genioglossus (Gg) muscles], and hyoid muscles [sternohyoid (Sh) and geniohyoid (Gh) muscles] during cortically induced rhythmic jaw and tongue movements (CRJTMs). These muscles were classified into two groups: group 1 was activated mainly in the jaw opening phase, and group 2 was activated mainly in the jaw closing and power phases. The Di, Gg, and Gh were included in the former, and the Ma, Sg, and Sh were included in the latter. 5. The timings of EMG activation to a jaw movement cycle were relatively constant for the muscles of group 1, irrespective of the types of CRJTMs, whereas those for the muscles of group 2 altered considerably with the different types of CRJTMs. 6. Relationships of the integrated muscle activity between the Di and Gg and between the Di and Gh were significant, whereas those between the Ma and Sg and between the Ma and Sh were not. 7. When a small strip of polyurethane form of various degrees of hardness was inserted between the opposing molars during CRJTMs, EMG activity of the muscles of group 2 increased with the hardness of the strip. On the other hand, EMG activities of the muscles of group 1 were less affected by the same intraoral stimuli. 8. Two conclusions were reached: first, physiological properties of the CRJTMs and cortically induced rhythmic movements of the hyoid were essentially similar to those observed in natural mastication. This fictive mastication might thus be regarded as a suitable model for simulating natural mastication.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Year:  1993        PMID: 8459287     DOI: 10.1152/jn.1993.69.2.569

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  17 in total

1.  Regional differences in length change and electromyographic heterogeneity in sternohyoid muscle during infant mammalian swallowing.

Authors:  Nicolai Konow; Allan Thexton; A W Crompton; Rebecca Z German
Journal:  J Appl Physiol (1985)       Date:  2010-06-10

2.  Identification of c-Fos immunoreactive brainstem neurons activated during fictive mastication in the rabbit.

Authors:  T Athanassiadis; K A Olsson; A Kolta; K-G Westberg
Journal:  Exp Brain Res       Date:  2005-05-11       Impact factor: 1.972

3.  Roles of intrinsic and extrinsic tongue muscles in feeding: electromyographic study in pigs.

Authors:  Mustafa Kayalioglu; Volodymyr Shcherbatyy; Amir Seifi; Zi-Jun Liu
Journal:  Arch Oral Biol       Date:  2007-03-12       Impact factor: 2.633

4.  Evolution of muscle activity patterns driving motions of the jaw and hyoid during chewing in Gnathostomes.

Authors:  Nicolai Konow; Anthony Herrel; Callum F Ross; Susan H Williams; Rebecca Z German; Christopher P J Sanford; Chris Gintof
Journal:  Integr Comp Biol       Date:  2011-06-24       Impact factor: 3.326

Review 5.  Generation of the central masticatory pattern and its modification by sensory feedback.

Authors:  James P Lund; Arlette Kolta
Journal:  Dysphagia       Date:  2006-07       Impact factor: 3.438

6.  Cerebellar cortical output encodes temporal aspects of rhythmic licking movements and is necessary for normal licking frequency.

Authors:  Jerí L Bryant; John D Boughter; Suzhen Gong; Mark S LeDoux; Detlef H Heck
Journal:  Eur J Neurosci       Date:  2010-06-28       Impact factor: 3.386

7.  Supratrigeminal Bilaterally Projecting Neurons Maintain Basal Tone and Enable Bilateral Phasic Activation of Jaw-Closing Muscles.

Authors:  Edward Stanek; Erica Rodriguez; Shengli Zhao; Bao-Xia Han; Fan Wang
Journal:  J Neurosci       Date:  2016-07-20       Impact factor: 6.167

8.  Localization of the central rhythm generator involved in spontaneous consummatory licking in rats: functional ablation and electrical brain stimulation studies.

Authors:  G Brozek; I A Zhuravin; D Megirian; J Bures
Journal:  Proc Natl Acad Sci U S A       Date:  1996-04-16       Impact factor: 11.205

9.  Anatomical organization of brainstem circuits mediating feeding motor programs in the marine toad, Bufo marinus.

Authors:  Rakesh Mandal; Curtis W Anderson
Journal:  Brain Res       Date:  2009-08-22       Impact factor: 3.252

10.  Internal kinematics of the tongue during feeding in pigs.

Authors:  Volodymyr Shcherbatyy; Zi-Jun Liu
Journal:  Anat Rec (Hoboken)       Date:  2007-10       Impact factor: 2.064

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.