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65 Cards in this Set

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upper motor neurons
neurons from central motor centers in the motor cortex, brainstem centers (midbrain, pons, medulla), cerebellum, basal ganglia, thalamus
lower motor neurons
located in brainstem from cranial nerve nuclei and the spinal cord (form motor nerves)
principal sources of input onto LMNs
1. supraspinal or descending motor pathways
2. spinal neurons (segmental interneurons and intersegmental neurons)
3. primary afferent (sensory fibers)
motor cortex
planning, initiating, and directing voluntary movements
basal ganglia
gating proper initiation of movement
brainstem centers
basic movements and postural control
cerebellum
sensory motor coordination (coordination/timing of movement)
local circuit neurons
reflex coordination
motor neuron pool
all of the motor neurons innervating a single muscle
dorsal horn of SC
sensory (laminae I-VI)
intermediate zone of SC
descending/sensory neurons (upper lamina VII)
ventral horn of SC
interneurons/motor neurons (lower VII, VIII, IX)
primary motor cortex
M1/area 4 caudal precentral gyrus into anterior bank of central sulcus; directs movement has a hommunculus, contralateral prjections, functional aspect (interjoint coordination), distributed so different muscles/joints at different areas
supplementary motor area/medial promoter area
M2/area 6b on the medial surface of the hemisphere above the cingulate gyrus; initiates movements specified by internal cues (spontaneous)
lateral premotor area
PM/area 6a just anterior to primary motor cortical strip of precentral gyrus; movements based on external cues
cingulate motor area
M3/area 24&25 on medial surface of hemisphere in limbic cortex; movements based on emotional state or reward information
thalamocortical projections
relay info from somatosensory system, vestibular system, cerebellum, and basal ganglia to motor areas
cerebellar info path
to M1/PMC after synapsing at VLp in posterior thalamus
basal ganglia info path
to SMA (some M1) after synapsing at VLa in anterior thalamus
large Betz cells
ballistic bidirectional movements, all-or-none, no sensory feedback, 10% of cortical layer V
small pyramidal cells
slow, accurate, unidirectional movement, tight sensory control, graded firing, 90% of cortical later V
muscle field
M1 neurons can influence multiple muscles
corticomotoneuronal cells
M1 cortical spinal neurons synapse directly onto spinal motoneurons (for distal skilled movements)
M1 lesions
cause permanent loss of fine motor control such as finger individuation
motor unit
a motor neuron and all of the muscle fibers to which it connects (basic unit of movement)
M2 lesions
impaired self-initiated tasks, bimanual coordination affected like manipulating fingers in both hands
somatosensory receptive fields
M1 neurons posses cutaneous or deep receptive fields via projections from S1
size principle
smallest motor units recruited first and then bigger as force increases
force
proportional to the number of motor units active at any given time
slow motor units
muscle fibers rich in mitochondria and myoglobin; energy efficient and fatigue resistant to produce small forces
fast-fatiguable motor units
sparse mitochondria; fatigue easily and produce large forces for brief periods of time
fast fatigue-resistant motor units
intermediate motor units that produce twice as much force as slow motor units
SMA lesion
impairment in planning self-initiated motor tasks; bimanual coordination impaired
lateral premotor cortex lesions
impairment in planning externally-cued motor tasks (object-related)
cingulate motor area lesions
defects in emotional state or reward information effects on motor control
extrafusal muscle fibers
generate force; innervated by alpha motor neurons
intrafusal muscle fibers
part of muscle spindle; innervated by gamma motor neurons
muscle spindles
stretch receptors; activated by change in muscle length and in rate of change of length; arranged in parallel with the extrafusal muscle fibers surrounding them
muscle spindle polar regions
contractile, receive gamma motor neuron innervation (controls the sensitivity of the spindle by contracting polar intrafusal fibers)
muscle spindle equatorial region
noncontractile, receive sensory information from Groups Ia and II afferents
gamma motor neurons
regulate sensitivity of the spindles to muscle stretch by setting the intrafusal muscle fibers to an appropriate length
group Ia afferents
large diameter, fast conducting nerve fibers that connect monosynpatically with the alpha motor neuron
group II afferents
terminate on interneurons in the spinal cord
alpha-gamma coactivation
gamma motor neurons activate spindle contraction as alpha neurons contract the muscle; maintains sensory feedback to CNS
Golgi Tendon Organ
records the tension generated at the myotendinous junction during contraction (in series with extrafusal muscle fibers)
Group Ib sensory axons
afferent fiber from GTO that contact inhibitory interneurons that decrease alpha motor activity innervating that muscle
LMN syndrome
flaccid paralysis, fasiculations, fibrillations (polio, ALS, spinal shock)
flaccid paralysis
weakness, hypotonia, hyporeflexia or areflexia, muscle atrophy
fasciculations
spontaneous brief contractions of motor units of injured alpha motor neurons (possibly normal, can be ALS)
fibrillations
spontaneous twitches of single denervated muscle fibers; not visible (electromyography), usually pathogenic
tectospinal tract
midbrain superior colliculus
rubrospinal tract
midbrain red nucleus
lateral vestibulospinal tract
pons lateral vestibular nucleus
medial reticulospinal tract
pons medial pontine reticular nuclei
lateral reticulospinal tract
medulla medial medullary reticular nuclei
anti-gravity muscles
lower limb extensors, upper limb flexors, axial extensors (Medial RST activates, Lateral RST inhibits)
muscle tone
resting level of tension in a muscle (depends on alpha neurons--depends on Ia spindles--depends on gamma motor neurons--gamma inhibited by UMN LReST)
decerebrate rigidity
cut below midbrain to block LReST (MReST and LVST still able to work) leading to uninhibited gamma motor neurons, increased Ia/II sensory and alpha (hypertonia/spasticity)
spasticity
characterized by hyperactive stretch reflexes (increase in sensitivity to rate of change of muscle length = velocity-dependent reflex activity)
clasp-knife type resistance
initial high level of resistance which suddenly yields as GTOs start firing
clonus
rhythmic, oscillatory contraction and relaxations of muscles in response to muscle stretching
rigidity (Parkinson's)
characterized by hypertonicity that is equally evident in both extensors and flexors (stretch reflexes are hypoactive)
UMN syndrome
spastic paralysis (weakness, hypertonia, hyperreflexia, positive Babinski's sign, spasticity, muscle atrophy)
alpha rigidity
LVST excitatory to alpha anti-gravity muscles but normally inhibited at vestibular nuclei by cerebrum/cerebellum (effect on alpha only, not reduced by gamma reflex)
cog-wheel resistance
Parkinson's rigidity in moving limb like a ratchet with tremors (defect in basal ganglia)