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Neural Control of Swallowing

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Facial Nerve (VII) for lip sphincter and buccal muscles; ... Paralysis of all muscles of facial expression (including those of the forehead) ... – PowerPoint PPT presentation

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Title: Neural Control of Swallowing


1
Neural Control of Swallowing
2
Neural Control of Swallowing
  • Deglutition is best understood as a specialized
    example of motor control.
  • It involves a dynamic interplay of descending
    motor tracts and ascending sensory tracts.
  • Cortical and subcortical motor systems, such as
    the cerebellum and the basal ganglia, play an
    important role in maintaining postural stability
    and head position.
  • Corticospinal and corticobulbar tracts carry
    inputs from cortical motor centers in the frontal
    lobe and converge on central pattern generators
    in the lower brainstem.

3
Motor Tracts
  • The motor cranial nerves participating in
    deglutition include
  • Trigeminal Nerve (V) for muscles of mastication
  • Facial Nerve (VII) for lip sphincter and buccal
    muscles
  • Glossopharyngeal (IX) and Vagus (X) Nerves for
    muscles of the palate, pharynx, esophagus,
    larynx, and respiratory control centers and
  • Hypoglossal Nerve (XII) for the extrinsic muscles
    of the tongue.

4
CN V Trigeminal Nerve
  • The trigeminal nerve is the largest cranial nerve
    and originates in the pons.
  • Its motor root supplies the muscles of
    mastication, some of the muscles of the soft
    palate, and the muscles inserting into the floor
    of the mouth.

5
CN V Trigeminal Nerve
  • Damage to the trigeminal nerve can affect the
    eating process.
  • Specific signs of trigeminal nerve damage or lack
    of innervation by the trigeminal nerve include
  • Absence/loss of bite reflex in children
  • Partial/total paralysis of the muscles of
    mastication, affecting mandible movement
  • Lock jaw, or trismus, resulting from tonic spasm
    or rigid contraction of the masseter, temporalis,
    or either pterygoid muscles.

6
CN VII Facial Nerve
  • The special visceral efferent fibers of the
    facial nerve supply muscles of facial expression,
    including the buccinator, as well as the
    posterior belly of the digastric, stylohyoid and
    stapedius muscles.
  • The general visceral efferent fibers innervate
    the lacrimal, submandibular, and sublingual
    glands, as well as mucous membranes of
    nasopharynx, hard and soft palate.

7
CN VII Facial Nerve
  • The general visceral efferent fibers innervate
    the lacrimal, submandibular, and sublingual
    glands, as well as mucous membranes of
    nasopharynx, hard and soft palate.
  • They originate from a diffuse collection of cell
    bodies in the caudal pons just below the facial
    nucleus known as the superior salivatory nucleus.

8
CN VII Facial Nerve
  • Signals for voluntary movement of the facial
    muscles originate in the motor cortex (in
    association with other cortical areas) and pass
    via the corticobulbar tract in the posterior limb
    of the internal capsule to the motor nuclei of CN
    VII.
  • Fibers pass to both the ipsilateral and
    contralateral motor nuclei of CN VII in the
    caudal pons.

9
CN VII Facial Nerve
  • The portion of the nucleus that innervates the
    muscles of the forehead receives corticobulbar
    fibers from both the contralateral and
    ipsilateral motor cortex.
  • The portion of the nucleus that innervates the
    lower muscles of facial expression receives
    corticobulbar fibers from only the contralateral
    motor cortex.
  • This is very important clinically as central
    (upper motor neuron) and peripheral (lower motor
    neuron) lesions will present differently.

10
CN VII Facial Nerve
  • Damage to the motor nucleus of CN VII or its
    axons results in a lower motor neuron lesion.
  • Paralysis of all muscles of facial expression
    (including those of the forehead) will be
    expressed ipsilateral to the lesion.
  • Damage to neuronal cell bodies in the cortex or
    their axons that project via the corticobulbar
    tract through the posterior limb of the internal
    capsule to the motor nucleus of CN VII are upper
    motor neuron lesions.
  • Voluntary control of only the lower muscles of
    facial expression on the side contralateral to
    the lesion will be lost.

11
CN VII Facial Nerve
  • Voluntary control of muscles of the forehead will
    be spared due to the bilateral innervation of
    that portion of the CN VII motor nucleus.
  • Upper motor neuron lesions are usually the result
    of stroke.
  • Damage to the facial nerve affecting the eating
    process can include
  • Decreased salivary production and mucosal
    dryness.

12
CN VII Facial Nerve
  • Loss of symmetry to mouth, which may droop to one
    side and
  • Inability of buccinator muscles to monitor and
    control food during chewing, causing food to slip
    outside molar surfaces and collect between gums
    and cheeks.

13
CN IX Glossopharyngeal Nerve
  • The general visceral efferent fibers innervate
    the ipsilateral parotid gland.
  • Salivation is produced in response to smelling
    food (mediated by the olfactory system).

14
CN IX Glossopharyngeal Nerve
  • The special visceral efferent fibers of the
    glossopharyngeal nerve work in close conjunction
    with the vagus nerve to supply motor fibers of
    the stylopharyngeus muscle and glands of the
    pharynx and larynx.
  • Signals for voluntary elevation and/or dilation
    of the pharynx by the stylopharygeus muscle
    originate in the pre-motor and motor cortex.
  • They pass via the corticobulbar tract in the
    posterior limb of the internal capsule to synapse
    bilaterally on the ambiguus nuclei in the
    reticular formation of the medulla.
  • Damage to the motor fibers of the
    glossopharyngeal nerve may contribute to
    difficulty or loss of the ability to move food
    through the pharynx because of decreased
    functioning of the pharyngeal constrictor
    muscles.

15
CN IX Glossopharyngeal Nerve
  • The special visceral efferent fibers of the
    glossopharyngeal nerve work in close conjunction
    with the vagus nerve to supply motor fibers of
    the stylopharyngeus muscle and glands of the
    pharynx and larynx.
  • Signals for voluntary elevation and/or dilation
    of the pharynx by the stylopharygeus muscle
    originate in the pre-motor and motor cortex.
  • They pass via the corticobulbar tract in the
    posterior limb of the internal capsule to synapse
    bilaterally on the ambiguus nuclei in the
    reticular formation of the medulla.

16
CN IX Glossopharyngeal Nerve
  • Damage to the motor fibers of the
    glossopharyngeal nerve may contribute to
    difficulty or loss of the ability to move food
    through the pharynx because of decreased
    functioning of the pharyngeal constrictor
    muscles.

17
CN X Vagus Nerve
  • The motor branches of the vagus nerve supply the
    voluntary muscles of the pharynx, soft palate,
    most of the larynx, and one muscle of the tongue.
  • Specifically, they supply the superior, middle,
    and inferior pharyngeal constrictor muscles.

18
CN X Vagus Nerve
  • In the soft palate, they supply the levator veli
    palatini muscles, the palatopharyngeal muscles
    (posterior faucial pillar), the palatoglossus
    muscles (anterior faucial pillar), and the
    intrinsic muscles of the larynx involved in
    abduction and adduction.

19
CN X Vagus Nerve
  • Signals for the voluntary movement of the muscles
    innervated by CN X originate in the pre-motor and
    motor cortex and pass via the corticobulbar tract
    in the posterior limb of the internal capsule to
    synapse bilaterally on each nucleus ambiguus in
    the reticular formation of the medulla.
  • Damage to the motor portion of the vagus nerve
    may contribute to swallowing difficulty because
    of decreased functioning of the muscles of the
    soft palate and the pharyngeal constrictors.

20
CN X Vagus Nerve
  • Specifically, difficulty or inability to elevate
    the soft palate on the affected side may result
    in regurgitation of fluids/foods through the
    nose.
  • On examination the soft palate droops on the
    affected side and the uvula deviates opposite the
    affected side due to the unopposed action of the
    intact levator palatini muscle.

21
CN XII Hypoglossal Nerve
  • The somatic motor portion of the hypoglossal
    nerve innervates all the intrinsic and most of
    the extrinsic muscles of the tongue.
  • It supplies three of the four extrinsic muscles
    of the tongue including genioglossus,
    styloglossus, and hyoglossus.

22
CN XII Hypoglossal Nerve
  • Signals for the voluntary control of the muscles
    of the tongue originate in the motor cortex and
    pass via the corticobulbar tract in the posterior
    limb of the internal capsule to synapse in
    contralateral hypoglossal nucleus (1) in the
    medulla.

23
Sensory Tracts
  • Ascending sensory tracts reflexively evoke motor
    programs via the central pattern generator and
    provide continual feedback to modulate the
    descending motor systems.
  •  The sensory cranial nerves participating in
    deglutition include the trigeminal nerve for
    sensations from the face and the facial nerve for
    taste on the anterior tongue the
    glossopharyngeal and vagus nerves for sensation
    from the posterior tongue, palate, pharynx, and
    larynx the glossopharyngeal nerves for posterior
    taste sensation.
  • Sensory inputs also arise from neck muscles and
    joints to provide information regarding head
    position which is critical in maintaining
    orientation toward the food source, optimizing
    swallow efficiency, and allowing for airway
    protection.

24
CN V Trigeminal Nerve
  • The sensory component of CN V transmits stimuli
    from the areas of the scalp, face, nasal cavity,
    teeth, and mouth, as well as from proprioceptors
    of the muscles of mastication.
  • Damage to the sensory branches of CN V can affect
    the eating process by causing pain, that can be
    experienced as brief, sharp, flashing periods
    (like that with a toothache), or slow,
    methodically spaced periods of pain.

25
CN VII Facial Nerve
  • The special afferent components of CN VII
    transmit taste sensation from the anterior 2/3 of
    tongue, hard and soft palates.
  • Chemoreceptors of the taste buds located on the
    anterior 2/3 of the tongue and hard and soft
    palates initiate receptor (generator) potentials
    in response to chemical stimuli.

26
CN VII Facial Nerve
  • The taste buds synapse with the first order
    special sensory neurons from CN VII which enter
    the brainstem and ascend to synapse with the
    second order neuron found in the nucleus tractus
    solitarius--also referred to as the gustatory
    nucleus.
  • Ascending secondary neurons originating from
    nucleus tractus solitarius project both
    ipsilaterally and contralaterally to synapse with
    the third order neurons of the ventral
    posteromedial (VPM) nucleus of the thalamus.

27
CN VII Facial Nerve
  • Tertiary neurons from the thalamus project via
    the posterior limb of the internal capsule to the
    area of the cortex responsible for taste.
  • Damage to the sensory branches of CN VII can
    cause temporary/permanent loss of the sense of
    taste on the anterior 2/3 of the tongue, as well
    as a loss of sensation to the face.

28
CN IX Glossopharyngeal Nerve
  • The special afferent branches of CN IX provide
    taste sensation from the posterior 1/3 of the
    tongue.
  • The general somatic afferent branches of CN IX
    provide general sensory information from the
    upper pharynx, and the posterior 1/3 of the
    tongue.
  • The general sensory fibers of CN IX mediate the
    afferent limb of the pharyngeal reflex in which
    touching the back of the pharynx stimulates the
    patient to gag (i.e., the gag reflex).
  • The efferent signal to the musculature of the
    pharynx is carried by the special visceral motor
    fibers of the vagus nerve.

29
CN IX Glossopharyngeal Nerve
  • Damage to the sensory branches of CN IX may
    result in the inability to discriminate taste
    sensations on the posterior 1/3 of tongue.
  • Loss of sensitivity in the soft palate and
    posterior part of tongue may result in reduced or
    absent gag reflex.

30
CN X Vagus Nerve
  • The special afferent component of CN X is a very
    minor component.
  • It provides taste sensation from the epiglottic
    region.
  • However, the general visceral afferent component
    provides information from the larynx and the
    esophagus.
  • Damage to the sensory branches of the vagus nerve
    may affect laryngeal sensation to food/liquid
    penetration.

31
Central Pattern Generator
  • Swallowing, like sneezing and orgasm, is a fixed
    action pattern.
  • It is involuntary and stereotyped, but typically
    has a stimulus threshold that must be reached by
    specific key stimuli before it is triggered and
    its expression does not require previous
    learning.
  • It is different from a simple reflex in that it
    can not be elicited by isolated nerve activation
    (e.g., gag reflex) but must instead conform to a
    highly codified stimulus pattern that produces a
    behavioral sequence of more elementary motor
    acts.
  • Different individuals produce almost identical
    behavioral responses to specific key stimuli, and
    once initiated, fixed action patterns continue
    until completion.

32
Central Pattern Generator
  • For swallowing, the fixed action potential is
    triggered by stimulation of several receptors.
  • Once triggered, pharyngeal swallowing behavior
    involves a complex sequential activation of at
    least 10 different muscle groups.
  • Both sensory and motor information are necessary
    for the initiation of the pharyngeal swallow.
  • Sensory input involved in the initiation in the
    swallow comes from CNs V, VII, IX, and X.
  • Information about motor movement comes from the
    muscle spindles in the tongue via the CN XII.

33
Central Pattern Generator
  • The swallowing response is elicited from an
    interneuronal network of dorsal and ventral
    reticular bodies that comprise the central
    pattern generator.
  • The interneurons of the central pattern generator
    mediate interactions between motor and sensory
    nuclei.

34
Central Pattern Generator
  • The dorsal interneurons (in blue) initiate and
    program (spatially and temporally) swallowing
    behaviors.
  • The ventral interneurons (in red) distribute the
    excitation to the swallowing motor nuclei.

35
Input Functions
  • Receptor fields on the posterior tongue (CN IX),
    fauces, tonsils, velum (CN IX), laryngeal
    vestibule and ventricle (CN X), as well as the
    mucosa of the valleculae and pyriform recesses
    (CN X) and the salivary glands (CN VII) are
    stimulated by the presence of the bolus.
  • They send sensory information via their
    respective fasciculi to the cell bodies
    comprising the nucleus tractus solitarius (NTS).
  • The NTS, located in the dorsal medulla, is
    comprised of the cell bodies of the sensory
    neurons of the facial (VII), glossopharyngeal
    (IX), and vagus(X) nerves clustered in a long
    single group.

36
Input Functions
  • In addition to receiving sensory input from
    oropharyngeal receptors, it receives excitatory
    motor input from structures involved in motor
    control, including the motor and premotor
    cerebral cortices, via cortico-reticular
    pathways.
  • The input information arriving at the NTS from
    various sensory receptors and motor structures is
    summed and if stimulus threshold is reached by
    these key stimuli then the NTS organizes the
    pre-programmed sequential spatial-temporal
    sequence of swallow and sends this information to
    the nucleus ambiguus (NA) to execute the
    specified motor sequence.

37
Input Functions
  • Threshold of stimulation depends on the frequency
    of the stimulus, suggesting that when the correct
    excitatory code is carried by the descending
    corticobulbar tract and the peripheral sensory
    inputs, swallowing is elicited.
  • Corticobulbar input is thought to influence only
    the duration and intensity of muscle activity
    pre-programmed by the NTS for involuntary swallow
    behavior.
  • Indeed, if the dorsal medulla is destroyed,
    electrical stimulation of specific cortical sites
    involved in swallowing input will not trigger a
    swallow.
  • Moreover, direct isolated stimulation of any of
    the cranial nerve nuclei DOES NOT evoke
    swallowing.

38
Output Functions
  • The NA consists of the cell bodies of the motor
    neurons of the glossopharyngeal (IX) and Vagus
    (X) nerves clustered in a single group.
  • It connects with the trigeminal (V), facial
    (VII), and hypoglossal (XII) motor nuclei.
  • All efferent information is sent via the NA to
    the striated muscles of the pharynx, larynx, and
    upper esophagus.
  • Specifically, this ventral brainstem area
    coordinates efferent impulse flow by way of
  • CNs V, X, and XII to the muscles of the
    oropharynx

39
Output Functions
  • by way of CN X to the muscles of the hypopharynx
  • by way of CNs V and XII to the extrinsic muscles
    of the larynx and
  • by way of CN X to the intrinsic muscles of the
    larynx and esophagus.
  • Microelectrode recording during swallow prove
    ventral interneurons of the NA discharge at
    specific times during the pharyngeal and
    esophageal stages of swallow.
  • The first detectable action is contraction of the
    mylohyoid muscles, preceding all other muscle
    contractions by 30-40 ms to elevate the larynx.

40
Output Functions
  • Then in sequence, there is activation of the
    posterior tongue (continues to move back toward
    pharynx), the superior constrictor muscles, the
    palatopharyngeus (elevates pharynx and larynx and
    closes nasopharyngeal isthmus) and the stylohyoid
    and the geniohyoid muscles, which move the larynx
    up and forward.
  • Pharyngeal constrictors fire in overlapping
    order.
  • The cricopharyngeus dilates and esophageal
    peristalsis commences at a velocity of between
    2-4 cm sec.
  • Direct stimulation of the NA or other ventral
    motor nuclei does not evoke swallowing.

41
Output Functions
  • Instead only contraction of individual muscles is
    produced.
  • This is because swallowing is a sequential
    pattern of muscle contraction established by the
    NTS.
  • The ventral regions require input from the dorsal
    medulla to complete a swallow.
  • There are also cross connections between the CPGs
    on the right and the CPGs on the left side of the
    brainstem.
  • Therefore, there is bilateral symmetry of
    pharyngeal swallow and either side of the
    brainstem can coordinate the pharyngeal and
    esophageal phases.

42
Cortical Involvement
  • Although the brainstem alone can excite muscle
    contraction similar to swallowing, the cortex has
    significant control over the initiation of
    swallowing and the level of neuromuscular
    activity of volitional swallowing.

43
Cortical Involvement
  • The swallowing cortex is a discrete area
    located in the supplemental motor area, anterior
    to M1.
  • It is important for time-ordered organization of
    movements, especially in sequential performance
    of multiple movements.

44
Cortical Involvement
  • It is important in initiation of voluntary
    movements.
  • Other cortical sites involved in swallowing are
    the bilateral anterolateral regions of the
    premotor cortex.
  • These areas are believed to coordinate the
    sequence of tongue and facial movements.
  •  

45
Cortical Involvement
  • The primary motor strip (M1) controls execution
    of specific body parts, with tongue, mouth, eye,
    hand, arm, head, trunk, torso, and lower limbs
    represented in a caudal-rostral fashion along the
    precentral gyrus.
  •  

46
Cortical Involvement
  • Research shows that the insula, in particular the
    anterior insula (AI), is involved in the
    coordination of the interaction of oral
    musculature, gustation and autonomic functions.


47
Cerebellum
  • Research on swallowing and the cerebellum is
    minimal.
  • Most documented studies are case studies that
    involve widespread lesions and not isolated
    cerebellar lesions.
  • PET results in normals have indicated that there
    is specific representation of the
    pharyngeal/esophageal stages of swallowing in
    left cerebellar hemisphere, and that the whole
    cerebellum is involved in the coordination,
    sequencing, and timing of the swallow.
  • It is thought the cerebellum integrates
    proprioceptive, vestibular, and motor planning
    information and then communicates with the
    cerebral cortex to produce smooth synergistic
    movements.


48
Biomechanics of Bolus Flow
  • The duration and characteristics of each phase of
    swallow depends on the type and volume of food
    being swallowed.
  • Therefore, there are many types of normal
    swallows that occur predictably based on the
    characteristics of the food swallowed and
    voluntary control.
  • Moreover, the frequency of deglutition varies
    with activity we swallow more when eating and
    we swallow less when sleeping.
  • Mean deglutition frequency is approximately 580
    swallows per day.
  • During sleep, periods of 20 minutes or may pass
    when no swallow occurs.


49
Volume Effects
  • Changes in bolus volume create the greatest
    systematic changes in the oropharyngeal swallow.
  • Small volume swallows, such as saliva, of 1 to 3
    ml, produce sequential swallow phases (oral
    phase, followed by pharyngeal swallow,
    pharyngeal, and esophageal phases).
  • Large volume swallows, as in cup drinking, of 10
    to 20 ml, produce simultaneous oral and
    pharyngeal phase activity in order to safely
    clear the large bolus from both the oral cavity
    and the pharynx.


50
Volume Effects
  • As bolus volume increases, the timing of the
    tongue base retraction to contact the anteriorly
    and medially moving pharyngeal walls occurs later
    in the swallow.
  • The tongue based and pharyngeal walls will not
    move toward each other and make contact until the
    tail of the bolus reaches the tongue base.


51
Viscosity Effects
  • Normal swallowing transit times are slower on
    thicker food.
  • Thin liquids are easily deformed and move more
    readily in response to gravity and compression.
  • Thus agility and coordination must be adequate to
    control the bolus and time its transit through
    the oral and pharyngeal chambers while protecting
    the airway.
  • Thin liquids, being almost completely deformable,
    will pass most easily through narrow sites in
    transit.
  • Thicker foods move more slowly in response to
    gravity and compression.


52
Viscosity Effects
  • The more viscose the bolus, the less agility and
    control required, and the more forgiving when
    timing of swallow and coordination of transit are
    impaired.
  • Nonetheless, as bolus viscosity increases,
    adequate transit becomes more reliant on strength
    and constriction--the pressure generated by the
    oral tongue, tongue base, and pharyngeal walls
    increases and muscular activity increases.


53
Viscosity Effects
  • Valve functions, such as VP closure, upper
    esophageal opening, and laryngeal closure also
    increase slightly in duration as viscosity
    increases.
  • As the bolus becomes less deformable, it is less
    likely to pass through narrow sites in transit,
    and may lodge above them instead.
  • Thicker foods also heighten sensory awareness of
    food.


54
Gustatory Effects
  • Despite the many substances we seem to taste,
    there are basically only four primary taste
    fundamentals sour, salt, bitter, and sweet.
  • The stimuli that the brain interprets as the
    basic tastessalty, sour, sweet, and bitter
    (possibly umamia glutamate), are registered via
    a series of chemical reactions in the taste cells
    of the taste buds.
  • We perceive all taste qualities all over our
    tongue, although there may be increased
    sensitivity to certain qualities in certain areas.


55
Gustatory Effects
  • Each of the four primary tastes is caused by a
    different response to different chemicals.
  • Certain regions of the tongue react more strongly
    than others to certain taste sensations although
    individual taste cells are not programmed or
    tuned to respond to only one kind of taste
    stimulus.
  • Flavor is a complex mixture of sensory input
    composed of taste (gustation), smell (olfaction),
    and the tactile sensation (chemical irritation)
    of food as it is being munched (mouthfeel).
  • Our taste system also provides information on the
    intensity and pleasantness (or unpleasantness) of
    taste as well.

56
Gustatory Effects
  • Neurons in the taste pathway record these
    attributes simultaneously, responding to touch
    and temperature stimuli as well.
  • Food preferences can be influenced by many
    factors, such as physiologic status, food
    context, familiarity, and environment.
  • There are three cranial nerves that supply taste
    buds the facial, glossopharyngeal, and vagus
    nerves.
  • Chemical irritation for mouthfeel is due to
    trigeminal stimulation, although the taste
    cranial nerves also perceive irritation.
  • Taste thresholds remain quite robust with aging,
    but loss of olfaction with aging is another
    story.

57
Gustatory Effects
  • We begin to lose our sense of smell by age 40,
    with significant, gradual decrements occurring
    each decade thereafter, reaching up to 70 loss
    by age 70.
  • When older adults complain that food doesnt seem
    to taste right, it is most likely the loss of
    smell (which diminishes flavor).
  • The threshold for taste varies for each of the
    primary tastes. 
  • Bitter substances have the lowest
    threshold--maybe a protective function.
  • The threshold for sour substances is somewhat
    higher than for bitter.

58
Gustatory Effects
  • The thresholds for salty and sweet substances are
    about the same and higher than both bitter and
    sour substances.
  • For taste receptor cells to be stimulated, the
    substances we taste must be in a solution of
    saliva so they can enter taste pores.
  • Pleasant tasting foods cause the secretion of
    large quantities of saliva.
  • Foods with unpleasant tastes tend to decrease
    saliva flow.
  • Foods with strong acid content, noxious
    substances, or extremely dry foods bring about a
    very watery saliva secretion.
  • Moist foods and those with larger particles tend
    to elicit saliva with a sticky, thick base.

59
Gustatory Effects
  • With age, taste and smell intensity are reduced,
    which may contribute to loss of interest in
    nutritious foods.
  • Some medications, such as tetracycline
    (antibiotic), lithium carbonate (an
    antipsychotic), penicillamine (an antiarthritic),
    and captorpril (an antihypertensive) can result
    in an unpleasant metallic taste in the mouth.

60
Basic Forces of Eating
  • There are five basic forces involved with eating.
  • Compression is the deforming of food using force,
    such as between the tongue and palate.
  • Adhesiveness is the attraction of food and an
    external surface, such as food sticking to the
    palate.
  • Tensile refers to extension of foods under force,
    such as the effects of the pharyngeal muscles on
    the bolus.
  • Shear refers to the cutting of food into pieces
    by forces that are not directly opposing, such as
    lateral movement of the molars during chewing.


61
Basic Forces of Eating
  • Fracture is the breaking of food by two directly
    opposing forces, such as the incisors biting
    through a cookie.
  • These forces are used in varying degrees,
    depending upon the nature of the food and its
    position within the oral/pharyngeal/esophageal
    continuum.
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