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74 Cards in this Set

  • Front
  • Back
Where do the upper motor neurons live?
Motor cortex; basal ganglia; cerebellum; brainstem
Where do the lower motor neurons live?
Spiral cord and brainstem. Directly innervate skeletal muscles (visceral muscles is by autonomic ns)
single motor neuron, its axon fibers and the muscle fibers that it innervates.
motor unit
group of motor neurons that innervate fibers within the same muscle
motor neuron pool
Compare small vs. large motor neurons
Small have a low innervation ratio and fine delicate control (e.g., for extraocular muscles)

Large have a high innervation ratio and work for force generation (e.g., gastrocnemius, 2000:1)
Where are the cell bodies of the lower motor neurons?
Ventral horn of spinal cord gray matter and in motor nuclei of the cranial nerves in brainstem
Where are the cell bodies of the upper motor neurons?
either in cortex or in brainstem centers (like nuclei such as vestibular nucleus)
How is the mapping/topography of motor neuron pools accomplished?
Neurons innervating axial musculature (eg postural muscles of trunk) are located medially. More distal motor neurons innervate more distal muscles.
intrafusal muscle fibers
muscle spindles embedded within connective tissue capsules in the muscle. innervated by sensory axons that send info to the CNS about length and tension of muscle
What are the α motor neurons?
Type of lower motor neuron that innervates the extrafusal muscle fibers (the striated muscle fibers that actually generate the forces needed for posture and movement)
What are the γ motor neurons?
Innervate muscle spindles. gamma motor neurons are involved in reflexes and are involved in adjusting the tension on muscle spindles.

Adjust sensitivity of muscle spindles.
T/F individual motor axons branch within muscles to synapse on many different fibers
T. There are many more muscle fibers than motor neurons.
Characteristics of S (slow) motor units
-Contract slowly
-Generate small forces
-Fatigue resistant
-Impt for activates requiring sustained muscular contraction
-recruited the most quickly
Characteristics of fast-fatigable (FF) motor units
-Larger α motor neurons
-Innervate larger, pale muscle fibers that generate more force
-Fibers have sparse mitochondria
-Especially impt for brief exertions
-Takes a lot of neural stimulation to recruit them
Characteristics of fast fatigue-resistant (FR) motor units
-Intermediate size
-Not as fast as FF but faster than S
-Generate 2x force of S
-More resistant to fatigue than FF
What is the size-recruitment principle?
Small motor units fire first, have the lowest threshold, and generate the least force.

Large motor units have higher threshold but generate more force. They fire last.
What is the order of recruitment for FR, FF, and S.
1) S
2) FR
3) FF
T/F Increasing stimulation within a motor neuron pool progressively activates larger and larger neurons that in turn generate more and more force.
T
What is the stretch reflex?
A sensory response to muscle stretch.

Muscle spindle afferents fire when muscle is stretched. This synapses with α motor neurons in ventral horn of spinal cord that innervate the same muscle and forms inhibitory connections with α motor neurons of antagonistic muscles (aka reciprocal innervation)
What is reciprocal innervation?
A sensory afferent forms excitatory connections with one muscle group and inhibitory connections with an opposing/antagonist muscle group. Allows for rapid contraction of muscle and simutaneous relaxation of the antagonist muscle.
What kind of afferents does the stretch/myotatic reflex use?
Group Ia (very fast) afferents in the muscle spindle.
What is unusual about the stretch/myotatic reflex?
It's monosynaptic. The sensory neuron directly synapses on the motor neuron. (basis of the knee, ankle, etc. reflexes tested)
What is the γ bias (aka γ gain)?
The level of the γ motor neuron activity. It can be adjusted by upper motor neurons pathways as well as local reflex circuitry.

If the gain is high, a small amount of stretch applied to the intrafusal fibers will produce large increases in the number of α motor neurons recruited.
What happens to the response of the Ia fiber as the muscle contracts

a) in presence of γ neurons
b) without γ neurons
a) there is no decrease in Ia firing during muscle shortening

b) the response of the Ia fiber decreases as the muscle contracts
T/F In general, the baseline activity of γ fibers is high if a movement is difficult and requires precise execution
T
What group of sensory axon is golgi tendon organ?
Ib (slightly smaller than the Ia axons that innervate muscle spindles)
WHat encapsulated afferent nerve ending is located at the junction of muscle and tendon?
Golgi tendon organ
T/F Golgi tendon organs are in parallel with muscle spindles
F. They're in series.
How are golgi tendon organs more sensitive to increases in muscle tension than stretch?
When a muscle actively contracts, force acts directly on the tendon, leading to an increase in the tension of the collagen fibrils in the tendon organ and compression of the intertwined sensory receptors.
How is the golgi tendon circuit a negative feedback system?
it decreases the activation of a muscle when exceptionally large forces are generated, protecting the muscle.

tends to maintain a steady level of force, counteracting forces that decrease force (fatigue) and increase
T/F Golgi tendon organ also responds to passive muscle stretch
F
What happens in the golgi (inverse myotatic) reflex?
When the Golgi tendon organ is stimulated by muscle tension there is an increase in Ib afferent activity.

Ib fibers synapse on inhibitory neurons in the spinal cord that in turn inhibits the activity of motor neurons innervating the homonymous muscle.

Ib fibers activity also causes an excitation of motor neurons innervating antagonist muscles.
very generally, what happens in the flexion reflex pathway?
A noxious stimulus leads to activation of local spinal cord circuits that flex/withdraw the affected limb and extend the unaffected side to provide balance/support.
What stimulates the flexion/withdrawal reflex?
Touch, temperature, and pain
What fiber types carry info in the flexion/withdrawal reflex pathway?
Flexor Reflex Afferents (FRAs). Group II, III (Aδ), and IV (C)
What happens to the ipsilateral side stimulated by the flexion/withdrawal reflex?
Flexor muscles on ipsilateral side are <b>stimulated</b>.

Extensors on ipsilateral side are <b>inhibited.</b>
What happens to the contralateral side stimulated by the flexion/withdrawal reflex?
Extensor muscles on contralateral side are <b>stimulated</b> while flexors on contralateral side are <b>inhibited</b>.
What are the following for the <b>stretch reflex</b>:

A) Stimulus (type of receptor)
B) Neuron afferent type
C) How many synapses?
D) Response
A) Muscle spindle
B) Ia
C) Monosynaptic
D) Contraction
What are the following for the <b>golgi reflex</b>:

A) Stimulus (type of receptor)
B) Neuron afferent type
C) How many synapses?
D) Response
A) Golgi tendon organ
B) Ib
C) Disynaptic
D) Relaxation
What are the following for the <b>flexor withdrawal reflex</b>:

A) Stimulus (type of receptor)
B) Neuron afferent type
C) How many synapses?
D) Response
A) Touch, temp, pain
B) II,III (A&delta;), IV(C)
C) Polysynaptic
D) Ipsilateral flexion, Contralateral extension
What are the four distinct but highly interactive motor subsystems?
Local circuits in spinal cord and brainstem, descending upper motor neuron pathways, basal ganglia, and cerebellum
Directly link the nervous system and muscles to form motor unit
&alpha; motor neurons located in spinal cord and cranial nerve nuclei
What are central pattern generators?
Specialized local circuits that provide much of spatial coordination and timing of muscle activation
What are symptoms of lower motor neuron syndrome?
Paralysis (loss of movement) or paresis (weakness)
Loss of reflexes (areflexia)
Loss of muscle tone
Muscle atrophy (with time)
Fasciculations (spontaneous twitches)
What kinds of neurons degenerate in ALS?
lower motor neurons in spinal cord and upper motor neurons in motor cortex
Symptoms of ALS?
Progressive muscle weakness, atrophy, muscle twitching.

Sensory function remains intact; mental status remains intact
Pyramidal pathways
Corticospinal, Corticobulbar. Have fibers passing thru and crossing in medullary pyramids
What are extrapyramidal structures responsible for?
Originate in brainstem centers. Responsible for control of posture and spatial orientation.
What are the extrapyramidal structures?
Red nucleus; superior colliculus; pontine and medullary reticular formation; vestibular nuclei
Rubrospinal tract: origin and function
Red nucleus; facilitation of flexors and inhibition of extensors
Difference between medial and lateral systems
Medial systems generally control axis/postural adjustment. Lateral systems do more peripheral movement, limbs in 3d, etc.
Pontine/medial reticulospinal tract:origin and function
pons; projects medially.

Has excitatory effect on LMNs.
<b>Maximum excitation on extensors</b>.
Which brainstem center has maximum excitatory effect on extensors?
Pontine/medial reticulospinal tract
Medullary/lateral reticulospinal tract:origin and function
medulla, projects laterally.

Inhibitory effect on LMNs.
<b>Maximum inhibition on extensors.</b>
Lateral vestibulospinal tract:origin and function
Deiter's nucleus.

Excitation of extensors and inhibition of flexors.

Has a "medial" function even though "lateral" is in name.
tectospinal/colliculospinal tract: origin and function
Superior colliculus. Fibers project to cervical spinal cord where they control neck muscles involved in head movement.
Effect of <b>motor cortex</b> on:

A) Extensors
B) Flexors
C) Pontine Reticular Formation
D) Medullary reticular formation
A)+
B) ++
C) -
D) +
Effect of red nucleus on:

A) Extensors
B) Flexors
A) -
B) +
Effect of pontine reticular formation on:

A) Extensors
B) Flexors
A) ++
B) +
Effect of lateral vesticular/Deiter's nucleus on:

A) Extensors
B) Flexors
A) +
B) -
Effect of Medullary reticular formation on:

A) Extensors
B) Flexors
A) --
B) -
What 3 things happen in spinal cord transection?
A) Complete loss of voluntary movements below lesion (paraplegia)
B) Loss of conscious sensations
C) Initial loss of reflexes
What is spinal shock?
Loss of reflexes and flaccid limbs following spinal cord lesion. It's the result of removal of background facilitation by higher centers on mostly &alpha; and &gamma; motor neurons. Partial recovery may occur due to hypersensitivity development.
What causes the initial loss of reflexes after spinal cord lesions?
Removal of excitatory influence of UMNs onto LMNs in spinal cord.
What causes the hyperreflexia occurring several weeks after spinal cord lesions?
Neurons in spinal cord recover and become hyperactive and hypersensitive due to build up of neurotransmitter.
What are the brainstem centers most impt to the maintenance of muscle tone in antigravity muscles?
Pontine reticular formation; deiter's nucleus/lateral vestibulospinal tract
What normally modulates/inhibits the excitatory effect on extensors of the pontine reticular formation?
central/cortical projections
What happens if there is a lesion above the level of the pontine reticular formation/mid-collicular cut?
Inhibitory influence of cortical projections is removed, leading to increase in tone of antigravity/postural muscles (mainly extensors).
What is decerebrate rigidity?
An increase in tone from the pontine reticular formation following removal of inhibitory cortical projections.

An exaggerated activation in muslce tone of extensors (arms and legs extended, back arched, head dorsiflexed, toes curled).
What happens if there is a lesion above the midbrain (red nucleus)?
No decerebrate rigidity because red nucleus still provides inhibition via rubrospinal tract on extensor activity.
What is the righting reflex? Stages of?
Refers to the ability of an animal to reflexively right itself from an abnormal position.

1) Input from vestibular system allows the head to orient into a normal vertical position
2) Distortion from neck muscles provide info to allow the trunk to come into alignment with the head.
What is decorticate rigidity?
Turning head to one side activates ipsilateral extensors and contralateral flexors.
Symptoms of upper motor neuron lesion
Weakness, spasticity (increased tone, hyperactive deep reflexes, clonus), Babinski's sign, Loss of fine voluntary movements
Symptoms of lower motor neuron lesion
Weakness or paralysis, decreased superficial reflexes, hypoactive deep reflexes, decreased tone, fasciculations and fibrillations, severe muscle atrophy