1/86
Looks like no tags are added yet.
What can prolonged misuse of a muscle cause?
Contractures
What is sensation necessary for?
Goal Directed Movement?
Use of sensory information to prepare for movement
Feedforward
Use of sensory information during or after a movement
Feedback
A decision is made in the anterior part of the frontal lobe, then ____
The Motor Planning Areas
Control Circuits
basal ganglia, cerebellum
Descending Tracts
Corticospinal Corticobrainstem Tracts
Spinal Interneurons
Influence type of info from LMN to Muscle
Lower Motor Neurons
Directly innervate skeletal muscle
Skeletal Muscle
Contract to produce movement
***Cerebral Motor Cortex and Brain Stem, Synapse with motor neuroms located in the brain stem and spinal cord. Basal Ganglia and Cerebellum adjust the activity of the descending tracts
Upper Motor Neuron
***Ventral Horn of spinal cord and brain stem, synapse with skeletal msucle fibers. spinal cord and brain stem determine activity
Lower Motor Neuron
Most common basal Ganglia Disorder
Death of Dopamine
Clinical Diagnosis involves HYPOKINESIS, RIGIDITY, and RESTING TREMOR
80% of Dopamine cells die before signs of disease appear
Onset age 50-79
Both Motor and Non-Motor Disease
Parkinsons Disease
4 Cardinal motor signs of PD
Tremor, Rigidity, Bradykinesia/Akinesia, Rigidity, Postural Instability
Are non-motor challenges if PD just as debilitating as motor challenges?
Yes
***lateral corticospinal tract
Most important pathway controlling voluntary movement of limbs.
Selective motor control
Ability to activate individual muscles independently
***Corticobrainstem Tract
Voluntary control of muscles in the head and neck
*** Upper facial Muscles are innervated___
Bilaterally
***Lower facial muscles are innervated____
Contralaterally
An interuption of corticobrainstem fibers will cause paralysis of ___ but not ____ facial muscles on opposite sides
Lower, Upper
***If a stroke creates a leision that disrupts the corticobrainstem pathway, the deficit will occur on the ______ _____ ____ because the upper face recieves bilateral projections. This is called Facial droop
Contralateral Lower Face
***Alpha Motor Neurons
Innervate the skeletal muscle and cause contraction
***Gamma Motor Neurons
Innervate the muscle spindle to help maintain its sensitivity to changes in muscle length
***An AMN and all the muscke fibers it innervates is known as the ____
Type 1 is slow twitch
Type 2 is fast twitch
Motor Unit
Henneman Size Principle
areas that require precision have more motor units while areas that require power have more muscle fibers per unit
Muscle Tone
Resistance to stretch
Hypotonicity
Loss of tone
Hypertonicity
Increased tone in muscle
Paresis
Weakness or inability to generate muscle force to produce movement
Paralysis
Total loss of volitional control
Hemiparesis
Weakness on half of body, Paralysis of one or more joints
Paraplegia
Paralysis of the trunk and legs
Tetraplegia
All 4 extremeties
***Hypertonia
UMN Lesions, Acute is LMN Lesions, basal Ganglia Disorders
***Hypotonia
LMN Lesions, Acute UMN Lesions, causes by brain hypoxia/ischemia/intercranial hemmorrhage/ and genetic disorders
***Decerebrate Rigidity
Lesion between midbrain and pons, Rigid EXTENSION of limbs and trunk, internal rotation of the UE and plantar flexion
***Decorticate Rigidity
Upper Midbrain or bilateral cerebral cortex, Upper limbs are FLEXED, lower limbs are extended
Spinal and cerebral shock
Occurs at time of insult, descending motor commands are interrupted and become inactive, Persons loses significant volitional movement and is largely paralyzed
***Babinski Reflexes
***Clonus
Abnormal reflex of involuntary, rhythmic contractions
***Atrophy
Loss of Muscle Bulk
***Disuse Atrophy
Loss of muscle bulk related to lack of use
***Neurogenetic Atrophy
From Damage to nervous system (Complete peripheral nerve lesion)
Areflexia
Decrease or loss of reflexes
Paresis
Decreased ability
Paralysis or flaccidity
Total Loss to generate muscle force
Poliovirus (LMN)
An Infection that targets motor neuron cell bodies an destroys them.
Post-polio Syndrome
Most common Lower motor neuron disease
Post-Polio
Muscle and joint weakness
fatigue
atrophy
breathing and swallowing problems
pain
sleep-related breathing disorders
decreased tolerance of cold temperatures
Parkinsons
brady/hypokinesia
termors
rigidity
postural instability
Basal-gangia disorder(UMN)- substansia Nigra
Amytropic lateral sclerosis (UMN and LMN)
Bilateral disease, Idiopathic, Progressive,
ALS
UMN+LMN
Paresis (Flaccidity and Rigidity)
Hyporeflexia, Hypotonia, Atrophy
Positive Babinski sign, Hyperreflexia, Atrophy
Brown Sequard Syndrome
Damage to half the cord
Pain/temp- contralateral
light touch/proprioception/sterignosis- ipsilateral
Loss occurs 2-3 dermatomes below due to collateral branching
Brown Sequard Syndrome
Ipsilateral UMN Lesions below the level of the lesion
Ipsilateral LMN Lesions at the level of the lesion (Flaccidity)
transverse cord
Loss of voluntary movement, pain/temp, DCML, Bladder(At or below T12) both sides
Anterior Cord
Affects anterolateral and lateral corticospinal tracts and LMNs within the cord
Loss of voluntary motor both sides
Loss of pain and temp both sides
Complete motor paralysis
Severe flexion injury
Position and vibration sense preserved
centeral Cord Syndrome
Cervical level lesion
Anterolateral pathway impairment (Hyperextension injury)
Loss of voluntary motor both sides
Loss of pain/temp both sides
Loss of DCML both sides
May Spare Sacral function
Posterior Cord Syndrome
loss of fine touch, pressure, vibration, and proprioception
Rare
SENSORY ATAXIA
Degenerative
Demyelinating disorders. External compression, Blockage of PSA
Sensory Ataxia
Decreased coordination, decreased proprioception, poor balance, decreased sensation or vibration and fine touch
Cerebellar Dysfunction
Doesn’t interfere with sensory perception or muscle strength.
Damage=Impaired coordination and postural control, decreased cognitive/social/emotional fucntion.
Ataxia
Jerky, innacurate movements
Dysarthria
Slurrred speach
Dysdiadochokinesia
Inability to preform rapidly repeating alternating movements
Dysmetria
Inability to accuratly move an intended distance
Action Tremor
Shaking during voluntary movement increased when approaching intended target
Basal Ganglia
Goal directed behavior
social behavior
Emotional/otivational circut
Oculomotor
Motor
What do diseases of the basal ganglia cause
Excessive movement or insufficient movement
Huntingtons Disease
Basal Ganglia(UMN) -Striatum
Autosomal dominant, Neurodegenerative
DNA Triplet Repeating
Symptoms are motor, cognitive, or psychiatric
life expectancy 15yrs
CHOREA(Involuntary jerky movements)
Difficulty decision making, organizing, planning, multitasking, progresses to dementia
Dystonia
Contraction of muscles yielding abnormal posture, twisting, and repetetive movements.
Genetic and non-progressive
No cure but managed with medications
Cervical dsytonia is the most common (Neck muscles twisting)
Gaze stabilization- maintain visual contact while head is moving
vestibulochloear reflex
Equilibrium and posture
Semicircular canals, utricle, and saccule
hearing
Cochlea
Vestibular Nerve Path
Semicircular ducts otholithic (Utricle and Saccule), Vestibular nerve, Vestibular nuclei (Up- vestibular cortex) (Down- Cerebellum), spinal cord
Vestibular nuclei send what kind of vestibular information to the vestibular cortex for conscious awareness?
Afferent
vestibular Apparatus
Semicircular ducts, utricle, and saccule
In addition to recieving input from semicircular canals, utricle, and saccule, they recieve ___?
Proprioceptive, tactile, and auditory information
The Vestibular Nuclei activate movements to support what?
Gaze and Equilibrium
Bony Labirynth
Cochlea, Vestibule, and Semicircular Canal
Cochlea (Anteromedial)
Hearing
Vestibule (Mid Portion)
Static Functions, connects cochlea and semicircular canal
maintains balance and orientation
Projections to brainstem
Semicircular canal (Posterior lateral)
Kinetic Functions
kinetic Labirynth
3 semicircular canals- hair cells that respond to motion of the endolymph
ROTATIONAL MOVEMENT (Right angles)
Cupula in ampulla that has hair cells in membrane that moves when head moves
Cupula- Directions, not right angles
Static Labirynth
Otolithic organs, utricle, and saccule
macular crystals bend and activate hair cells
LINEAR ACCELERATION AND DEACELERATION
Nystagmus
Involuntary back and forth eye movement
Benign paroxysmal Positional Vertigoo:Canalithiasis
acute onset of vertigo and nystagmus. Rapid head change can result in dizziness, subsiodes in 2 minutes
Cause: Crystals from otolithic organs (Utricle and Saccule) float into semicircular canals and create abnormal sensations of head movement
Vestibular Neuritis
inflammation of vestibular nerve caused by a virus
Unsteadiness, nausea, vertigo
Last up to 3 days
Unaffected hearing
Meiniers Disease
Abnormal fluid pressure in inner ear
Sensation of fullness, tinnitus, vertigo, nausea, vomiting, hearing loss
Can occur spontaneously without head movement