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Explain why speech is a fine motor skill
o Accuracy and speed
o Uses knowledge of results
o Improves with practice
o Motor flexibility
o Relegates to automatic control
Define motor learning:
Development of internal predictive models (core motor plans) that result from practice or experience
Explain the 4 motor learning characteristics
o Improvement
o Consistency/Stability
o Persistence
o Adaptability
Linguistic-symbolic planning
a. Phonological planning: selection and sequential combination of phonemes in accordance with phonotactic rules of language
b. Non-motor
c. Language areas Wernicke’s and Broca’s are highly active during this level
d. Impairment: aphasia
Motor Planning:
a. Transformation of symbolic units to code for the motor system
b. Goal-oriented, articulator-specific, motor goals: spatial and temporal
c. During motor planning:
i. Core motor plans are recalled from sensorimotor memory during speech
ii. Plan consecutive movements
iii. Adaptation of specifications
d. Articulator specific
e. Impairment: AOS
Motor Programming
a. Set of muscle commands structured before movement sequence begins that can be delivered without external feedback
b. Muscle specific, what allows us to move our articulators
c. Impairment: AOS and some dysarthria’s
Motor execution:
a. Programs to muscles and joints to movement (with feedback)
b. Motor cortex, lower motor neurons, peripheral nerves, motor units, control (basil ganglia and cerebellum)
c. Execution and control of muscle commands
d. Impairment: dysarthrias
Contrast motor planning from motor programming
o Planning:
Strategy (articulator): what are we doing
High level
Dominant hemisphere
o Programming:
Tactics (muscle): how are we going to do it
Middle level
Both hemispheres
Planning
Strategy (articulator): what are we doing
High level
Dominant hemisphere
Programming
Tactics (muscle): how are we going to do it
Middle level
Both hemispheres
Define motor speech disorders (MSDs)
Speech disturbances resulting from neurologic impairments affecting the planning, programming, control, or execution of speech. MSDs include the dysarthrias and apraxia of speech.
Dysarthria
collective name for a group of neurologic speech disorders that reflect abnormalities in the strength, speed, range, steadiness, tone, or accuracy of movements required for the breathing, phonatory, resonatory, articulatory, or prosodic aspects of speech production.
Can result from CNS and PNS damage, results in weakness, incoordination, involuntary movements, and changes in muscle tone
Lesion location determines speech deficits
Impaired execution and control
Apraxia of speech
a neurologic speech disorder that reflects an impaired capacity to plan or program sensorimotor commands necessary for directing movements that result in phonetically and prosodically normal speech.
results from CNS damage
Results in inability to recall motor plans, relay motor plans, organize movements, and adapt motor plans
impaired planning and programming NOT due to weak musculature or fatigue
aphasia
language disturbance
Describe the 5 speech subsystems
Respiration
Phonation
Resonance
Articulation
Prosody
Respiration
speak on exhalation (use expired airflow to produce speech)
Allows us the medium to produce speech
Disturbances may result in:
Decreased words per breath
Abnormal loudness
Abnormal vocal quality
Phonation
voice (varying pitch)
Disturbances may result in:
Abnormal vocal quality (dysphonia)
Resonance
degree to which voice is transmitted through oral versus nasal cavities
Disturbances may result in:
Hypernasality: Air escaping through nose during oral sounds
Articulation
Specific, distinguishable sounds that when combined give meaning
Disturbances can result in:
Distorted speech
Prosody
all of the speech systems working together, pertains to stress, intonation, and rhythm of speech to convey stress, emphasis, and emotion, important for speech naturalness
Disturbances can result in:
Prolonged phonemes, decreased/equal stress, monopitch/monoloudness, abnormal rate
Define prosody
all of the speech systems working together, pertains to stress, intonation, and rhythm of speech to convey stress, emphasis, and emotion, important for speech naturalness
Identify the “gold standard” method for diagnosing MSD
Perceptual methods rely primarily on the auditory perceptual attributes of speech. They are the gold standard for clinical differential diagnosis, judgments of severity, many decisions about management, and the assessment of meaningful temporal change.
Important when reading the literature, did the authors appropriately describe the characteristics of the participants’ speech? This helps with external validity
Anatomy
study of structures of the human body
Physiology
study of the function of each of these structures
Sagittal
right/left
Coronal (frontal)
front and back halves
Transverse
top and bottom
oblique
diagonal
Ventral
towards the front or belly
Dorsal
towards the back
CNS
Brain and spinal cord
PNS
Ganglia and Nerves
Gray matter
nerve cell bodies and dendrite
White
axons
Describe the 2 pyramidal tracts
Corticobulbar: head and neck
Corticospinal: trunk and limbs
Nerve:
groups of fibers that travel together in the PNS.
Tracts
groups of fibers that travel together in the CNS.
cell body
integrates incoming impulses, maintains cell function
Dendrites
receives impulses from other cells and sends to cell body
Axon
Carries impulses from cell body to another cell
· Explain importance of myelination and identify cells that provide myelin to the CNS and PNS
Speeds up neural transmission (increases nerve’s conduction velocity by about 120 meters/sec), myelin also appears to protect axons from injury.
Schwann cells in the PNS form myelin, which wraps around fibers in most peripheral nerves.
Oligodendroglia cells are the source of myelin in the CNS.
Commissural
homologous areas between hemispheres
Association
areas within a hemisphere
Projection
higher and lower centers
Dura mater:
outermost membrane. It consists of two layers of fused tissues that separate in certain regions to form the intracranial venous sinuses, areas where blood drains from the brain.
Arachnoid
lies beneath the dura and is applied loosely to the surface of the brain.
Pia mater
the thin innermost layer, is closely attached to the brain’s surface. The
Explain functions of CSF
Its primary functions are to cushion the CNS against physical trauma and to help maintain a stable environment for neural activity.
Mechanical protection
Pathway for metabolic and nutritional compounds to reach CNS
Removes waste
Immune function
Frontal (lobe)
Executive function, personality, learning, behavior, emotion, movement, language, sensation
Temporal
Memory, language, hearing, learning
Parietal
Touch, integration of sense, arithmetic and spelling, spatial relationships
Occipital
Vision
Identify the major function of thalamus
serves as a relay center, as all information entering the cortex goes through a specified part of this structure, depending on the type of information being conveyed. Relay center for motor and sensory information (except olfaction)
Explain the functional importance of the Circle of Willis
Supplies both the cerebral lobes and the brainstem, cerebellum, and cervical spine. (provides blood flow to brain via 3 cerebral arteries)
Identify 3 parts of the brainstem
Midbrain (upper)
Pons (middle)
Medulla (lower)
Explain the functions of brainstem
Provides a communicative link between the brain and the spinal cord
Regulates critical life functions (respiration, heart rate, blood pressure, and swallowing)
Houses majority of cranial nerve nuclei
Explain the functions of basal ganglia as it pertains to motor performance
a group of subcortical nuclei involved in facilitating or inhibiting the initiation and amount of movement.
Important role in movement:
Initiation of movement
Amount, direction and sequence of movement
Supportive movements
Postural control
Muscle tone
Cognitive and emotional functions
Explain the functions of cerebellum as it pertains to motor performance
important for maintaining muscle tone, balance, and coordination
Regulates muscle tone
Motor planning/programming
Coordinates timing/sequence of movements and “smooths” movements (reciprocal connections with other structures and feedback)
Language, cognitive, and emotional functions
Pyramidal
direct motor system, only one synapse
Function: initiation of skilled, voluntary movement
Courses from the cortex -> internal capsule -> brainstem/spinal cord
Extrapyramidal
indirect motor system
Multiple synapses
Diffuse system of subcortical structures and pathways
Function: regulates and modulates (adjusts) movements; regulates reflexes
Posture, tone, balance, coordination
Identify 2 tracts of the pyramidal system (comprise the UMN system)
Corticobulbar
Corticospinal
Corticobulbar tract
muscles of the head and neck, eye movements, speech and swallowing
Cortex -> brainstem -> cranial nerves
Corticospinal tracts:
lateral corticospinal fibers cross at medullary pyramids, anterior corticospinal fibers cross in spinal cord
Typical CNs
UMNs innervate brainstem nuclei on both sides
CNs V, VII, IX, X, XI, XII (most)
Atypical CNs
UMNs innervate brainstem nuclei on contralateral side
CNs VII, XI, XII
Agonist
muscle that causes specific movements to occur through its own contraction
Antagonist
muscle that acts in opposition to the specific movement by the agonist
Slow Motor (Type I):
slowly fatiguing red fibers (10-20 impulses/sec)
Fast Motor (Type II):
rapidly fatiguing white fibers (30-60 impulses/sec)
Spatial summation
more motor units activated, the greater strength and force
Temporal summation
faster a motor unit is stimulated, the greater the strength and force
Define muscle tone
internal state of muscle fiber tension at rest
Proprioceptive Feedback:
All speech muscles are striated, most striated muscles have muscle spindles, but, NOT all speech muscles have muscle spindles
Focal
involving a single area or continuous group of structures (e.g., left frontal lobe)
Multifocal
2+ areas of >1 group of contiguous structures
Diffuse
involving roughly symmetric portions of the nervous system bilaterally (e.g., generalized cerebral atrophy associated with dementia)
Acute
within minutes (as related to development of symptoms)
Subacute
within days
Chronic
within weeks/months (as related to development of symptoms)
UMN Lesions
spastic paralysis
hypertonia
weakness
hyperreflexia
Pathological reflexes
Atrophy
Normal nerve conduction belocity
No denervation potentials on EMG
Clonus
LMN Lesions
Flaccid paralysis
hypotonia
(more Weakness)
Hyporeflexia
Areflexia
Fasciculations
(More) atrophy
Abnormal nerve conduction velocity
Denervation potentials on EMG
Paralysis
results if a muscle is deprived of input from all of its LMNs (complete loss of movement)
Paresis
incomplete loss of movement
CHI (closed head injury)
often associated with more diffuse abnormalities.
PHI (penetrating head injury)
can produce relatively focal neurologic abnormalities, dura mater was penetrated
Coup injuries
Focal lesion often occur at the site of impact and result in focal neurologic deficits
Coup Contrecoup injuries
injury associated with acceleration, the motion of the brain may also cause trauma at sites opposite the point of impact, focal lesion at site of impact AND lesion at opposite point
Ischemic Stroke
Due to a blockage
Thrombosis:
narrowing/occlusion (type of ischemia)
Embolism
traveled embolus
Hemorrhagic
due to a bursting vessel/bleeding
Aneurysm
ballooned blood vessel
Arteriovenous malformation (AVM):
abnormally formed blood vessels
Hypokinesia
Reduced mobility, (too little movement)
associated with disease of the SN substantia nigra, which results in a deficiency of dopamine in the basal ganglia. The effect is an increase in muscle tone that, unlike in spasticity, is not velocity dependent and is present throughout the range of motion of limbs; the result is increased resistance to movement, a condition known as rigidity.
Parkinson’s disease
Hyperkinesia
Excessive movements, (too much movement)
result from excessive activity in dopaminergic nerve fibers, thereby reducing the circuit’s damping effect on cortical release of unwanted, competing motor programs. This results in involuntary movements (e.g., chorea, athetosis, and dystonia) that can vary considerably in their locus, speed, regularity, and predictability.
Huntington’s disease
Ataxia
abnormal, uncoordinated movements, cerebellar damage
Myoclonus
involuntary single or repetitive brief, lightning-like jerks of body part(s)
Chorea
involuntary rapid, nonstereotypic, random, purposeless movements of a body part
Dystonia
involuntary abnormal postures resulting from excessive co-contraction of agonist and antagonist muscles
Ballismus
gross, abrupt contractions of axial and proximal extremity muscles