Literature DB >> 2051192

Effects of reversible inactivation by cooling of the primate face motor cortex on the performance of a trained tongue-protrusion task and a trained biting task.

G M Murray1, L D Lin, E M Moustafa, B J Sessle.   

Abstract

1. Intracortical microstimulation (ICMS) and surface stimulation studies of primate face motor cortex have shown an extensive representation within face motor cortex devoted to movements of the tongue and face; only a very small representation for jaw-closing movements has ever been demonstrated. These data suggest that face motor cortex plays a critical role in the generation of tongue and facial movements but is less important in the generation of jaw-closing movements. Our aim was to determine whether disruption of primate face motor cortical function would indeed interfere with the generation of tongue movements but would not interfere with the generation of jaw-closing movements. 2. The face motor cortex was reversibly inactivated with the use of cooling in two monkeys that were trained to perform both a tongue-protrusion task and a biting task. Recording of single neuronal activity in the cortex beneath the thermode confirmed the reversible inactivation of the cortex. Each task involved a series of trials in which the monkey was required to produce a preset force level for a 0.5-s force holding period; the monkey received a fruit-juice reward if it successfully completed a task trial. Cooling of the ICMS-defined face motor cortex was achieved bilaterally or, in one experiment, unilaterally by circulating coolant through thermodes placed either on intact dura overlying face motor cortex in both monkeys or directly on the exposed pia in one of the monkeys;thermode temperature was lowered to 3-5 degrees C during cooling. Electromyographic (EMG) recordings were also made from masseter, genioglossus, and digastric muscles. 3. During bilateral cooling of the thermodes on the dura overlying the face motor cortex, there was a significant reduction in the success rates for the performance of the tongue-protrusion task in comparison with control series of trials (i.e., precool and postcool) in which the thermodes were kept at 37 degrees C. Quantitative analyses of force and EMG activity showed that the principal deficit was an inability of each monkey to exert sufficient force with its tongue for a sufficient length of time onto the tongue-protrusion task transducer; this deficit was paralleled by a reduction in the level of genioglossus and digastric EMG activity. At 4 min after commencement of rewarming, task performance had returned to control, precool levels.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 2051192     DOI: 10.1152/jn.1991.65.3.511

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


  13 in total

1.  One hour of tongue-task training is associated with plasticity in corticomotor control of the human tongue musculature.

Authors:  P Svensson; A Romaniello; K Wang; L Arendt-Nielsen; B J Sessle
Journal:  Exp Brain Res       Date:  2006-02-18       Impact factor: 1.972

2.  Intracortical modulation of cortical-bulbar responses for the masseter muscle.

Authors:  Enzo Ortu; Franca Deriu; Antonio Suppa; Elena Giaconi; Eusebio Tolu; John C Rothwell
Journal:  J Physiol       Date:  2008-05-22       Impact factor: 5.182

3.  Cortical innervation of the hypoglossal nucleus in the non-human primate (Macaca mulatta).

Authors:  Robert J Morecraft; Kimberly S Stilwell-Morecraft; Kathryn M Solon-Cline; Jizhi Ge; Warren G Darling
Journal:  J Comp Neurol       Date:  2014-05-14       Impact factor: 3.215

4.  Modulation dynamics in the orofacial sensorimotor cortex during motor skill acquisition.

Authors:  Fritzie I Arce-McShane; Nicholas G Hatsopoulos; Jye-Chang Lee; Callum F Ross; Barry J Sessle
Journal:  J Neurosci       Date:  2014-04-23       Impact factor: 6.167

5.  Overdrinking, swallowing inhibition, and regional brain responses prior to swallowing.

Authors:  Pascal Saker; Michael J Farrell; Gary F Egan; Michael J McKinley; Derek A Denton
Journal:  Proc Natl Acad Sci U S A       Date:  2016-10-10       Impact factor: 11.205

6.  Differential effects of local inactivation within motor cortex and red nucleus on performance of an elbow task in the cat.

Authors:  J H Martin; S E Cooper; C Ghez
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

Review 7.  The role of the cerebral cortex in swallowing.

Authors:  R E Martin; B J Sessle
Journal:  Dysphagia       Date:  1993       Impact factor: 3.438

8.  Corticocortical projections to representations of the teeth, tongue, and face in somatosensory area 3b of macaques.

Authors:  Christina M Cerkevich; Hui-Xin Qi; Jon H Kaas
Journal:  J Comp Neurol       Date:  2014-02-15       Impact factor: 3.215

9.  Plasticity in corticomotor control of the human tongue musculature induced by tongue-task training.

Authors:  Peter Svensson; Antonietta Romaniello; Lars Arendt-Nielsen; Barry J Sessle
Journal:  Exp Brain Res       Date:  2003-06-26       Impact factor: 1.972

10.  Jaw movement dysfunction related to Parkinson's disease and partially modified by levodopa.

Authors:  L T Robertson; J P Hammerstad
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-01       Impact factor: 10.154

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