Literature DB >> 19428638

Effects of tongue force training on orolingual motor cortical representation.

David J Guggenmos1, Scott Barbay, Crystal Bethel-Brown, Randolph J Nudo, John A Stanford.   

Abstract

Previous research has demonstrated that training rats in a skilled reaching condition will induce task-related changes in the caudal forelimb area (CFA) of motor cortex. The purpose of the present study was to determine whether task-specific changes can be induced within the orofacial area of the motor cortex in rats. Specifically, we compared changes of the orofacial motor cortical representation in lick-trained rats to age-matched controls. For 1 month, six water-restricted Sprague-Dawley rats were trained to lick an isometric force-sensing disc at increasing forces for water reinforcement. The rats were trained daily for 6 min starting with forces of 1g, and increasing over the course of the month to 10, 15, 20, 25 and finally 30 g. One to three days following the last training session, the animals were subjected to a neurophysiological motor mapping procedure in which motor representations corresponding to the orofacial and adjacent areas were defined using intracortical microstimulation (ICMS) techniques. We found no statistical difference in the topographical representation of the control (mean=2.03 mm(2)) vs. trained (1.87 mm(2)) rats. This result indicates that force training alone is insufficient to drive changes in the size of the cortical representation. We also recorded the minimum current threshold required to elicit a motor response at each site of microstimulation. We found that the lick-trained rats had a significantly lower average minimum threshold (29.1+/-1.0 microA) for evoking movements related to the task compared to control rats (34.6+/-1.1 microA). These results indicate that while tongue force training alone does not produce lasting changes in the size of the orofacial cortical motor representation, tongue force training decreases the current thresholds necessary for eliciting an ICMS-evoked motor response.

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Year:  2009        PMID: 19428638      PMCID: PMC2680792          DOI: 10.1016/j.bbr.2009.02.020

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  26 in total

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2.  Neuronal activity patterns in primate primary motor cortex related to trained or semiautomatic jaw and tongue movements.

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3.  Comparison of electrical thresholds for evoking movements from sensori-motor areas of the cat cerebral cortex and its relation to motor training.

Authors:  S Ghosh; A H Koh; A Ring
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5.  Excitation of pyramidal tract cells by intracortical microstimulation: effective extent of stimulating current.

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6.  Age-related changes in orolingual motor function in F344 vs F344/BN rats.

Authors:  Hongyu Zhang; Crystal S Bethel; Susan E Smittkamp; John A Stanford
Journal:  Physiol Behav       Date:  2007-10-12

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

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8.  Cortical synaptogenesis and motor map reorganization occur during late, but not early, phase of motor skill learning.

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9.  Aged Fischer 344 rats exhibit altered orolingual motor function: relationships with nigrostriatal neurochemical measures.

Authors:  John A Stanford; Elena Vorontsova; Stewart P Surgener; Greg A Gerhardt; Stephen C Fowler
Journal:  Neurobiol Aging       Date:  2003 Mar-Apr       Impact factor: 4.673

10.  Differential effects of aging on fore- and hindpaw maps of rat somatosensory cortex.

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  6 in total

Review 1.  Role of exercise in maintaining the integrity of the neuromuscular junction.

Authors:  Hiroshi Nishimune; John A Stanford; Yasuo Mori
Journal:  Muscle Nerve       Date:  2013-12-17       Impact factor: 3.217

2.  Differential effects of amphetamine and GBR-12909 on orolingual motor function in young vs aged F344/BN rats.

Authors:  Susan Smittkamp; Heather Spalding; Hongyu Zhang; John A Stanford
Journal:  Psychopharmacology (Berl)       Date:  2014-06-13       Impact factor: 4.530

3.  Effects of Tongue Force Training on Bulbar Motor Function in the Female SOD1-G93A Rat Model of Amyotrophic Lateral Sclerosis.

Authors:  Delin Ma; Jeffrey M Shuler; Aishwarya Kumar; Quincy R Stanford; Sudheer Tungtur; Hiroshi Nishimune; John A Stanford
Journal:  Neurorehabil Neural Repair       Date:  2016-09-24       Impact factor: 3.919

4.  Tongue force and tongue motility are differently affected by unilateral vs bilateral nigrostriatal dopamine depletion in rats.

Authors:  Andrea L Nuckolls; Cole Worley; Christopher Leto; Hongyu Zhang; Jill K Morris; John A Stanford
Journal:  Behav Brain Res       Date:  2012-07-14       Impact factor: 3.332

5.  Active zone protein Bassoon co-localizes with presynaptic calcium channel, modifies channel function, and recovers from aging related loss by exercise.

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Journal:  PLoS One       Date:  2012-06-06       Impact factor: 3.240

6.  Tongue Force Training Induces Plasticity of the Lingual Motor Cortex in Young Adult and Aged Rats.

Authors:  Miranda J Cullins; Julie M Wenninger; Jared S Cullen; John A Russell; Jeffrey A Kleim; Nadine P Connor
Journal:  Front Neurosci       Date:  2019-12-19       Impact factor: 4.677

  6 in total

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