Class 6 Flashcards

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1
Q

Cortical areas associated with motor processes and descending tracts

A
  • Frontal lobe
    • Precentral gyrus, primary motor cortex (M1), Area 4
    • Adjacent cortex, supplementary and premotor cortex (Area 6)
  • Parietal lobe
    • Post-central gyrus, primary somatosensory projection area (S1), Areas 3-1-2
    • Second somatosensory, Area 5
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2
Q

humunculus

A
  • Map of body on lateral surface of M1 and S1 cortex
    • Distortion in map represents number of cortical cells projecting to muscles of a particular body part
    • Much larger areas associated with muscles of face, speech apparatus, hands (precision of motor control)
    • Electrical stimulation of a specific area within motor cortex yields muscle contraction of specific body part; damage (e.g. stroke) produces paralysis of those muscles
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3
Q

What is the corticospinal tract?

A

Direct pathway to spinal cord; output from motor cortical areas (“pyramindal” tracts)

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4
Q

Describe the corticospinal tract.

A
  • Crossed: lateral corticospinal tract
    • Projects to motor neurons and interneurons supplying muscles (eg. hands)
    • Mediates fine motor control of limbs and hands (e.g. reaching and manipulation)
  • Uncrossed: ventromedial corticospinal tract
    • Projects to spinal interneurons which, in turn, project to motor neurons supplying proximal muscles
    • Mediates axial movement and postural control
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5
Q

Describe the indirect pathways to the spinal cord.

A

“Extrapyramidal”; more precisely designated as corticobulbar projections to brain stem nuclei which then give rise to several descending pathways (e.g. cortex to red nucleus: rubrospinal tract; cortext to reticular nuclei: reticularspinal tract)

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6
Q

Describe the motor tracts originating in the motor cortex.

A
  • Corticospinal tract
    • Lateral corticospinal tract: fingers, hands, arms, lower leg, and feet
    • Ventral corticospinal tract: trunk and upper legs
  • Corticobulbar tract
    • Face and tongue
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7
Q

Describe the motor tracts originating in the subcortex.

A
  • Ventromedia tracts
    • Vestibulospinal tract: leg and lower trunk movement, control of posture
    • Tectospinal tract: head and upper trunk movement, visual tracking
    • Lateral reticulospinal tract: flexor muscles of the legs
    • Medial reticulospinal tract: extensor muscles of the legs
  • Rubrospinal tract
    • Hands, lower arms, lower legs, and feet
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8
Q

What are the inputs to the motor cortical areas?

A
  1. Cortical areas associated with sensory/perceptual processes (e.g. visual, somatosensory, auditory)
  2. Cortical/subcortical processes associated with motivational processes (limbic system)
  3. “Loops” involving the cerebellum and basal ganglion
    • The basal ganglia or the cerebellum do not give rise to pathways that directly descend to the spinal cord
    • Output from these structures is to cortical motor areas or brain stem nuclei
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9
Q

Describe the function, parts, and disorders associated with the basal ganglia.

A
  • Integrates movement and control of posture
  • Caudate nucleus, putamen, globus pallidus
  • Disorders: cerebral, Parkinson’s disease, Huntington’s disease, ballismus
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10
Q

Describe the inputs to and outputs from the cerebellum.

A
  • Inputs: climbing fibers, mossy fibers
  • Outputs: purkinje cells, basket cells (inhibitory influence)
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11
Q

Cerebellar damage may cause…

A
  • Intentional tremor: at onset or termination of movement
  • Disruption of coordination (asynergies, dysarthrias)
  • Locomotor ataxia and postural disturbances
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12
Q

Describe spinal cord output motor neurons.

A
  • Cell bodies located in anterior gray (ventral horn)
  • Axons exit cord through ventral root (motor) and join with dorsal root (sensory) to form spinal nerve (mixed) to supply muscles and sensory receptors
  • Axon endings terminate on motor end plate of muscle fiber
    • Release ACh, opens Na+ channels, causes AP, muscle contracts (shortening of muscle fiber brought about by interdigitation of action and myosin - sliding filament theory)
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13
Q

Describe neuromuscular relationships.

A
  • A given muscle fiber typically supplied only by one motorneuron
  • Motor neuron pool: all motor neurons innvervating one muscle
  • Motor unit: motor neurons terminate on many muscle fibers (endings diverge); all muscle fibers supplied by one motor neuron are activated as a unit when impulse travels down axon
  • Innervation ratio: number of muscle fibers supplied by one axon (10:1 yields less precise force gradation than 3:1)
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14
Q

What are the two types of motor neurons?

A
  1. alpha motor neurons: terminate on extrafusal fibers resulting in the generation of force and motion at joints
  2. gamma motor neurons: terminate on intrafusal fibers attached to the muscle spindle (a sensory receptor) resulting in regulating the sensitivity of this receptor (efferent control of afferent input)
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15
Q

Describe the gamma motor system.

A
  • Small motor neurons originating in the spinal cord
  • Innervate the distal ends of intrafusal fibers
  • This contraction actiates the stretch reflex
  • The result is increased muscle tone
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16
Q

Describe the inputs to the spinal cord.

A
  • Tracts from brain stem nuclei and motor cortext descend in white matter and terminate on interneurons and motor neurons in gray matter
  • Afferents from receptors located in the skin, joints, and muscles (spindle, tendon Golgi body) enter cord through dorsal root
    • Axons ascend to terminate in brain
    • Axon collaterals terminate on interneurons and motor neurons contributing to local reflexes
17
Q

Describe the monosynaptic reflex (myotactic stretch reflex).

A
  • Muscle stretch is transduced by muscle spindle (a sensory receptor) and leads to action potentials in Group IA afferents
  • Group IA afferents enter cord through dorsal roots and synapse with MNs that innervate that same muscle (as was stretched) causing contraction
  • Monosynaptic stretch reflex: maintains position; intrafusal fibers serve as detectors
    • When stretched, receptor activated; sends signals to motor neuron activating extrafusal fibers; their increased contraction reduces stretch; works because connected in series with extrafual fibers
  • Reciprocal innervation: muscles arranged in pairs that act in opposite directions at a joint (agonists/antagonists); for joint displacement, agonist/antagonist MN pools activated in opposite direction (excitation of agonist MN, inhibition of antagonist MN)
18
Q

Describe the multisynaptic reflex.

A
  • Flexor withdrawal reflex
  • Sensory inputs from pain receptors (or pressure and thermal receptors at high-intensity stimulation) terminate on interneurons
  • After interneuronal synapses, input to MN that broadly activate flexor muscles and inhibit extensor (on same side as input; reverse pattern on opposite side of body)
  • Involves 3 or more neurons; receptor sends signal to spinal cord and synapses on interneuron; interneurons may excite and/or inhibit to accomplish a withdrawal reflex
19
Q

Describe cerebral palsy.

A
  • A disability caused by brain damage before or during birth or in the first years, resulting in a loss of voluntary muscular control and coordination. It is non-progressive and results in activity limitation.
  • Statistics:
    • ~2 in 1000 births
    • 10% postnatal
    • ~500,000 individuals in the US
20
Q

Describe the causes of cerebral palsy.

A
  • Usually caused by damage to one or more specific areas of the brain, usually during fetal development; before, during, shortly following birth, or during infancy
  • CP in term infants most often reflets phenomena preceding the onset of labor
  • CP in preterm infants more often include prenatal and perinatal factors
  • Major risks are low birth weight and birth asphyxia (often involving CNS maldevelopment); the latter is usually associated with quadriplegia
  • Other factors include physical trauma, abnormalities of neural migration, viral agents (rubella, cytomegalovirus) and toxoplasmosis
  • Multiple births constitute 10% of CP
21
Q

What are the three main types of cerebral palsy?

A
  1. spastic (pyramidal): still and difficult movement (hemiplegia, diplegia, quadraplegia)
  2. athetoid (extrapyramidal): involuntary and uncontrolled movement
  3. ataxic: disturbed sense of balance and depth perception

* There may be a mixture of these types for any individual.

22
Q

What are the treatment options for cerebral palsy?

A
  • pharmacological: reduce muscle tone, seizures
  • surgical: tendon release, transfer
  • physical/occupational/speech therapy
  • neuroplasticity (practice-induced brain changes arising from repetition, increasing movement complexity, motivation, and reward) plays a large role
  • Early and intensive treatments