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Craniofacial Muscles

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12 Tongue Structure and Function

223

age-related muscle decline, although it does not mitigate motoneuron loss or prevent

sarcopenia. Hypoglossal motoneurons also receive inputs from numerous central and

peripheral sources, and it is possible that this rich synaptic milieu supports hypoglossal

nucleus motoneurons during dysfunction in any one projection system.

12.7 Conclusions

The architectural and neural specialization of the tongue re fl ects its unique lack of

skeletal constraints. Deformations of the tongue during oromotor behaviors are varied

and are not well described by activation of classically de fi ned muscles. Tongue

muscle architecture is complex and tongue motor units occupy limited territories,

enabling localized contraction of fi bers with different orientation that is needed to

achieve the dimensional control required by the muscular hydrostat model. The

extent to which the nervous system actually uses the fi ne-grained control structure

during routine behavior is not yet clear.

The tongue appears to be composed of conventional skeletal muscle fi bers with

speci fi c structural and control adaptations that re fl ect an unusually high degree of

daily activity and the absence of skeletal constraints on motion. In many species

tongue muscles are comprised principally of two conventional MHC isoforms. In

the rat, tongue motor unit contraction times are similar to those of other fast appendicular

motor units but produce much less force likely re fl ecting a low number of

muscle fi bers per motor unit.

Compared to appendicular muscles, tongue motor units have high duty cycles,

whether constitutively active to maintain airway patency or phasically active during

respiration or swallowing. Highly localized and small motor units may require high

fi ring rates for meaningful force production. Persistent activation of many motor

units may require high mitochondrial content and capillarization and protect tongue

muscles from typical aging dysfunction.

Acknowledgements We thank Audrey Jernigan for illustrations. This work was supported by

grant DC005017 from the National Institute on Deafness and Other Communication Disorders .

References

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with special reference to the cat. J Anat 73(pt 1):15–30

Abd-El-Malek S (1939) On the relationship between the epiphysis cerebri and the reproductive

system. J Anat 73(pt 3):419–423

Abd-El-Malek S (1955) Observations on the movements of the human tongue. II. J Egypt Med

Assoc 38(12):743–771

Agbulut O, Noirez P et al (2003) Myosin heavy chain isoforms in postnatal muscle development

of mice. Biol Cell 95(6):399–406

Aldes LD (1995) Subcompartmental organization of the ventral (protrusor) compartment in the

hypoglossal nucleus of the rat. J Comp Neurol 353(1):89–108

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