Module 3 Flashcards

1
Q
  • neural pathways that control the sequence and pattern of muscle contractions
  • distributed throughout brain and spinal cord
A

Motor System

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2
Q
  • consists of a single motor neuron and the muscle fibers that it innervates
  • for fine control, a single motor neuron innervates only a few muscle fibers
  • EXAMPLE: eye muscle
  • for larger movements, a single motor neuron may innervate thousands of muscle fibers
  • EXAMPLE: postural muscles
A

Motor Unit

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3
Q
  • is the set of motoneurons innervating fibers within the same muscle
A

motoneuron pool

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4
Q
  • force of muscle contraction is graded by recruitment of additional motor units (graded response)
  • as additional motor units are recruited, more motor neurons are involved and more tension is generated
A

Size Principle of Muscles

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5
Q

Types of Motor Neurons

A
  1. Alpha Motor Neurons

2. Gamma Motoneurons

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6
Q
  • innervate extrafusal skeletal muscle fibers
  • action potentials in α motor neurons lead to action potentials in the extrafusal muscle fibers they innervate, which results in contraction
A

Alpha Motor Neurons

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7
Q
  • innervate specialized intrafusal muscle fibers
  • adjust the sensitivity of the muscle spindles(so that they respond appropriately as the extrafusal fibers contract and
    shorten)
A

Gamma Motor neurons

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8
Q

Types of Muscle Fibers

A
  • Extrafusal Fibers

- Intrafusal Fibers

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9
Q
  • make up the bulk of muscle
  • innervated by alpha motor neurons
  • provide the force for muscle contraction
A

Extrafusal Fibers

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10
Q
  • smaller than extrafusal muscle fibers
  • are innervated by gamma motor neurons
  • encapsulated in sheaths to form muscle spindles
  • are too small to generate significant force
A

Intrafusal Fibers

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11
Q
  • central role in skeletal muscle control
  • cell bodies are topographically arranged within the ventral horn of the spinal cord
  • axons innervate skeletal muscle fibers
  • cell bodies receive numerous synaptic connections from:
    o proprioceptors
    higher levels of the CNS including the brainstem, basal ganglia, cerebellum, and motor cortex
A

Alpha Motor Neuron

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12
Q

Topographic Arrangement

A
  • muscles of the trunk are medial
  • muscles of the extremities are lateral
  • limb flexors are dorsal
  • limb extensors are ventral
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13
Q

¥ synapse with the pool of motor neurons by which they are stimulated
¥ predominantly inhibitory
¥ bring about recurrent or feedback inhibition

A

Renshaw Cells

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14
Q

What type of synaptic arrangement is exemplified by Renshaw cells?

A

one to many

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15
Q

What neurotransmitter is released by Renshaw cells?

A

Glycine

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16
Q

What type of neuronal circuit is exemplified by Renshaw cells?

A

Divergent

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17
Q

sense of awareness of:

  • position of the body in space
  • progress of the movement by sensory receptors within the muscles and joints
A

Proprioception

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18
Q
  • mechanoreceptors within muscles and joints

- provide the CNS with information regarding muscle length, position and tension (force)

A

Proprioceptors

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19
Q

More than half of all the nerve fibers that ascend and descend in the spinal cord are __.

A

Propiospinal fibers

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20
Q

two major proprioceptors:

A

O Muscle Spindle

O Golgi Tendon Organ

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21
Q
  • small, encapsulated intrafusal fibers
  • lie in parallel with extrafusal muscle fibers
  • send information to the nervous system about muscle length or rate of change of length
  • innervation is as follows:
    1. efferents via gamma motor neurons - regulates sensitivity of the spindles
    2. afferents via group Ia (primary or annulospiral endings) and group II fibers (secondary endings) - respond to muscle stretch
A

Muscle Spindles

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22
Q

True or False

The finer the movement required, the greater the number of muscle spindles in a muscle.

A

True

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23
Q

Types of Intrafusal Fibers in Muscle Spindles

A
  1. Nuclear Bag Fibers
    o detect the rate of change in muscle length (fast, dynamic changes)
    o innervated by group Ia afferents
    o have nuclei collected in a central “bag” region
2. Nuclear Chain Fibers
o detect static changes in muscle length
o innervated by group II afferents
o more numerous than nuclear bag fibers
o have nuclei arranged in rows
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24
Q

Role of Muscle Spindles

A
  • comparators for maintenance of muscle length
  • important during goal-directed voluntary movements
    o voluntary changes in muscle length are initiated by motor areas of the brain
    o includes changes to the set-point of the muscle spindle system
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25
Q
  • simultaneous activation of extrafusal fibers (by alpha motor neurons) and intrafusal fibers (by gamma motor neurons)
  • readjusts the sensitivity of muscle spindles continuously as the muscle shortens
  • allows the muscle spindles to be functional at all times during a muscle contraction
A

Co-activation

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26
Q
  • mechanoreceptors that lie within the tendons of muscles immediately beyond their attachments to the muscle fibers
  • respond to degree of tension within muscles
  • group Ib afferent fibers relay this information to the CNS (in particular the spinal cord and cerebellum)
A

Golgi Tendon Organ

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27
Q
  • rapidly executed, automatic, and stereotyped response to a given stimulus
  • simplest form of irritability associated with the nervous system
A

Reflex

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28
Q
  • neurons participating in a reflex form a reflex arc, which includes:
    o receptor
    o afferent neuron that synapses in the CNS
    o efferent neuron that sends impulses to an effector
    o interneurons may be present between the afferent and efferent neurons
A

Reflex arc

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29
Q

Afferent vs Efferent

A

Remember SAME!

Sensory = Afferent
Motor = Efferent
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30
Q

Classification of Neural Reflexes

A
  1. Efferent division that controls the effector
  2. Integrating region within the Nervous system
  3. Time at which the reflex develops
  4. The number of neuron in the reflex pathway
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31
Q

Classification of Neural Reflexes: Efferent division that controls the effector

A

a. Somatic motor neurons - control skeletal muscles

b. Autonomic neurons - control smooth and cardiac muscle, glands, and adipose tissue.

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32
Q

Classification of Neural Reflexes: Integrating region within the Nervous system

A

a. Spinal reflexes do not require input from the brain

b. Cranial reflexes are integrated within the brain

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33
Q

Classification of Neural Reflexes: Time at which the reflex develops

A

a. Innate (inborn) reflexes are genetically determined.

b Learned (conditioned) reflexes are acquired through experience

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34
Q

Classification of Neural Reflexes: The number of neuron in the reflex pathway

A

a. Monosynaptic reflexes have only two neurons: one afferent (sensory) and one efferent. Only somatic motor reflexes can be monosynaptic.
b. Polysynaptic reflexes in crude one or more interneurons between the afferent and efferent neurons. All autonomic reflexes are polysynaptic because they have three neurons: one afferent and two efferent.

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35
Q
  • also known as patellar tendon-tap reflex, knee-jerk reflex or myotactic reflex
  • stretching of a muscle stimulates the muscle spindle afferents
    plays an important role in the control of posture
A

Muscle Stretch Reflex

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36
Q

Components of a Muscle Stretch Reflex

A
  1. Dynamic Stretch Reflex

2. Static Stretch Reflex

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37
Q
  • caused by rapid stretch or unstretch
  • transmitted from primary sensory or annulospiral endings of the muscle spindles
  • oppose sudden changes in muscle length
  • lasts within a fraction of a second only
A

Dynamic Stretch Reflex

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38
Q
  • elicited by the continuous static receptor signals
  • transmitted by both primary and secondary endings
  • causes the degree of muscle contraction to remain reasonably constant
  • continues for a prolonged period
A

Static Stretch Reflex

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39
Q

Damping Function of Stretch Reflexes

A
  • muscle spindles prevent oscillation or jerkiness of body movements
  • ensure that contraction is relatively smooth, even though the motor nerve to the muscle is excited at a slow frequency
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40
Q
  • reinforcement technique for eliciting deep tendon reflexes
    o fingers are locked together and one hand pulls against the other while reflex is evoked
  • physiologic basis
    o when one muscle is stretched, it facilitates a substantial number of alpha motor neurons
    o transient increase of gamma motor neuron activity
A

Jendrassik’s Maneuver

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41
Q

Jendrassik’s maneuver facilitates multiple alpha motor neurons. What does this mean?

A

easier recruitment

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42
Q

If they are being facilitated, where are they located in the neuronal pool?

A

facilitated pool (it’s easier to excite)

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43
Q
  • oscillation of a stretch reflex

- ordinarily occurs only when the stretch reflex is highly sensitized by facilitatory impulses from the brain

A

Clonus

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44
Q
  • elicited by noxious stimuli
  • transmitted by group II, III, IV fibers
  • possesses at least one interneuron, and so the most basic flexion reflex is disynaptic
  • usually many muscles are involved through polysynaptic pathways
  • to achieve withdrawal of a limb:
    o flexor muscles in the limb must contract while the extensor muscles relax
A

Flexor Withdrawal Reflex

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45
Q

What type of neuronal circuit is exemplified by flexor withdrawal reflex?

A

Divergent

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46
Q

Receptor that senses pain

A

Nociceptor

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47
Q
  • supports the body as the weight shifts away form the painful stimuli
  • stimulation of the flexion reflex frequently elicits extension of the contralateral limb about 250 ms later
  • long latency between flexion and crossed extension represents the time taken to recruit interneurons
  • helps to maintain posture and balance
A

Crossed extensor reflex

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48
Q
  • ensures that the extensor muscles acting on a joint will relax while flexor muscles contract
  • neuronal circuit that causes this reciprocal relation is called reciprocal innervation
A

Reciprocal Inhibition

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49
Q

Components of Flexor Withdrawal Reflex

A
  • diverging circuits to spread the reflex to the necessary muscles for withdrawal
  • reciprocal inhibition circuits to inhibit the antagonist muscles
  • circuits to cause afterdischarge lasting many fractions of a second after the stimulus is over
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50
Q

What type of neuronal circuit is exemplified by prolonged afterdischarge in crossed extensor reflex?

A

Reverberating/Recurrent

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51
Q
  • Golgi tendon organs monitor muscle tension
  • negative feedback mechanism that prevents development of too much tension on muscles
  • when tension becomes extreme, reflex inhibitory effects lead to instantaneous relaxation of the entire muscle (lengthening reaction)
A

Inverse Myotactic Reflex

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52
Q

What are the four major spinal cord reflexes?

A
  1. Muscle Stretch Reflex
  2. Golgi Tendon reflex
  3. Flexor withdrawal reflex
  4. Crossed extension reflex
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53
Q

of synapses: Monosynaptic
stimulus: Muscle stretch
afferent fibers: Group Ia fibers
efferent response: Muscle contraction

A

Muscle Stretch Reflex

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54
Q

of synapses: Di/polysynaptic
stimulus: Muscle tension
afferent fibers: Group Ib fibers
efferent response: Muscle relaxation

A

Golgi Tendon reflex

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55
Q

of synapses: Polysynaptic
stimulus: Pain
afferent fibers: Group II, III, IV fibers
efferent response: Ipsilateral muscle flexion

A

Flexor withdrawal reflex

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56
Q

of synapses: Polysynaptic
stimulus: Pain
afferent fibers: Group II, III, IV fibers
efferent response: Contralateral muscle extension

A

Crossed extension reflex

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57
Q
  • caused by transection of the spinal cord
  • loss of spinal reflexes (areflexia) and flaccid paralysis below the level of the injury
  • over the ensuing weeks, spinal cord activity below the level of the lesion returns as the excitability of undamaged neurons increases
  • may give rise to spasticity of the paralyzed muscle groups
A

Spinal Shock

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58
Q

Events in Spinal Shock

A
  • Neurogenic Shock
  • Areflexia
  • Incontinence
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59
Q
  • arterial blood pressure falls instantly

- demonstrates that sympathetic nervous system activity becomes blocked almost to extinction

A

Neurogenic Shock

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60
Q
  • may last 2 weeks to several months

- order of return: stretch reflexes, flexor reflexes, postural antigravity reflexes, remnants of stepping reflexes

A

Areflexia

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61
Q
  • sacral reflexes for control of bladder and colon evacuation are suppressed
A

Incontinence

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62
Q
  • impairment or loss of motor and sensory function in the arms, trunk, legs, and pelvic organs
A

Tetraplegia / Quadriplegia

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63
Q
  • impairment of function of the legs and pelvic organs
A

Paraplegia / Biplegia

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64
Q
  • total paralysis of the arm, leg, and trunk on the same side of the body
  • does not usually result from spinal cord injuries but from strokes
A

Hemiplegia

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65
Q
  • polysynaptic reflex useful in testing for spinal shock
  • checks anal sphincter contraction in response to squeezing the glans penis
    o absence indicates spinal shock
    o first reflex to return after spinal shock
  • once this reflex has returned, all remaining neurologic deficits are considered permanent
A

Bulbocavernosus Reflex

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66
Q
  • contains motor areas- stimulation will elicit contralateral movements
  • displays somatotopic arrangement
  • areas of the body that are capable of especially refined and complex movements (i.e. fingers, lips, and tongue) have a disproportionately large area of representation
A

Cerebral Cortex

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67
Q
  • divided into three sub-areas, each of which has its own topographical representation of muscle groups and specific motor functions:
    o PRIMARY MOTOR CORTEX
    o PREMOTOR AREA
    o SUPPLEMENTARY MOTOR AREA
A

Motor Cortex

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68
Q
  • located in precentral gyrus or Brodmann area 4
  • responsible for the execution of movement (programmed patterns of motor neurons and voluntary movement)
  • is somatotopically organized (motor homunculus)
A

Primary Motor Cortex

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69
Q

Epileptic events in the primary motor cortex cause __

A

Jacksonian seizures

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70
Q
  • immediately anterior to the lateral portion of the primary motor cortex
  • forms a portion of Brodmann area 6
  • responsible for generating a plan for movement - transferred to primary motor cortex for execution
  • stimulation causes activation of groups of muscles
A

Premotor Area

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71
Q
  • located in the medial portion of Brodmann area 6 just anterior to the lower extremity portion of the precentral gyrus
  • stimulation causes activation of bilateral muscle activation (usually upper extremities)
  • programs complex motor sequences
  • active during mental rehearsal for a movement
A

Supplementary Motor Area

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72
Q
  • motor speech area

- converts simple vocal utterances into whole words and complete sentences

A

Broca’s Area

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73
Q
  • controls conjugate eye movement required to shift gaze from one object to another
A

Frontal Eye Field (Brodmann Area 8)

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74
Q
  • enables movement of head correlated with eyes
A

Head Rotation Area

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75
Q
  • when damaged, hand movements are lost (motor apraxia)
A

Area For Fine Movements Of Hand

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76
Q
  • carried by the corticospinal (pyramidal) and extrapyramidal tracts
  • also sends numerous collaterals to the basal ganglia, cerebellum and brainstem
A

Motor Outflow of Cerebral Cortex

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77
Q
  • motor areas receive inputs from many sources
    o predominant sensory input is from the somatosensory system, which receives its input from the thalamus
  • afferent information is also received from the visual system, cerebellum, and basal ganglia
    o used to refine movements, particularly to match the force generated in specific muscle groups to an imposed load
A

Motor Input of Cerebral Cortex

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78
Q

What are the three sub-areas of the motor cortex?

A

Primary Motor Area- execution of movement
Premotor Area - planning of movement
Supplementary Motor Area - bilateral muscle movement

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79
Q
  • originates over a wide area of cortex including both motor and somatosensory areas
  • more than 80 per cent of the fibers decussate at the pyramids (cervicomedullary junction)
  • predominant pathway for the control of fine skilled manipulative movements of the extremities
  • loss of precise hand movements is a hallmark feature of lesions to the corticospinal tract
A

Corticospinal Tract

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80
Q

CORTICOSPINAL TRACT

A
  • Motor Cortex
  • Corona radiata
  • Internal capsule
  • Cerebral peduncle
  • Brainstem
  • Cervicomedullary junction*
  • Corticospinal tract (A/L)
  • Anterior horn cell
  • Ventral root
  • Peripheral nerve
  • Neuromuscular junction
  • Muscle
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81
Q
  • conveys nerve impulses from the motor cortex to skeletal muscles of the head and neck
  • axons of UMNs descend from the cortex into the brain stem, where some decussate and others do not
  • provide input to lower motor neurons in the nuclei of cranial nerves III, IV, V, VI, VII, IX, X, XI, and XII
  • control voluntary movements of the eyes, tongue and neck, chewing, facial expression and speech
A

Corticobulbar Tract

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82
Q
  • also called Cerebrovascular Disease
  • cessation of blood flow to the brain due to:
    o ruptured blood vessel that bleeds into the brain
    o thrombosis of a vessel, producing local ischemia
  • muscles controlled by the damaged areas show a corresponding loss of function
    o clumsiness and loss of fine muscle control
    o postural movements may not be affected
    o hyperreflexia, hypertonia and spasticity occur with extension of involvement
A

Strokes

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83
Q
  • due to lesions to supplementary and premotor areas
  • loss of the ability to prepare for voluntary movement
  • ability to execute simple movements is retained
A

Apraxia

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84
Q
  • above the anterior horn cell
  • motor neurons that originate in the motor region of the cerebral cortex or the brain stem
  • main effector neurons for voluntary movement in layer V of the primary motor cortex (Betz cells)
  • UMN pathways (above anterior horn cell) include:
    ▪ corticospinal tract
    ▪ corticobulbar tracts
    ▪ extrapyramidal tracts
A

Upper Motor Neuron

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85
Q
  • below the anterior horn cell
  • motor neurons connecting the brainstem and spinal cord to muscle fibers
  • bring nerve impulses from the upper motor neurons out to the muscles
  • begins at the level of the anterior horn cell in the spinal cord
A

Lower Motor Neuron

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86
Q
  • total loss of motor function associated with an increase in muscle tone
  • associated with clasp-knife phenomenon and hyperreflexia
A

Spastic Paralysis

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87
Q
  • total loss of motor function associated with a decrease in muscle tone
  • associated with floppiness, areflexia or hyporeflexia
A

Flaccid Paralysis

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88
Q
  • reflex extension of the great toe with flexion of the other toes
  • evoked by stroking the lateral sole of the foot
  • presence indicates an upper motor neuron lesion
A

Babinski Reflex

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89
Q
  • small, local, involuntary muscle contractions visible under the skin
  • arise from spontaneous discharge of a bundle of skeletal muscle fibers
  • presence indicates a lower motor neuron lesion
A

Fasciculations

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90
Q
muscle tone: Increased
paralysis: Spastic Paralysis
deep tendon reflex: Hyperreflexia
babinski sign: Present
clonus: Present
fasciculations: Absent
atrophy: Atrophy of Disuse
A

Upper Motor Neuron (UMN) Lesion

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91
Q
muscle tone: decreased
paralysis: Flaccid Paralysis
deep tendon reflex: Hypo/Areflexia
babinski sign: Absent
clonus: Absent
fasciculations: Present
atrophy: Atrophy of Denervation
A

Lower Motor Neuron (LMN) Lesion

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92
Q
  • composed of midbrain, pons and medulla
  • special functions include:
    o control of respiration
    o control of the cardiovascular system
    o partial control of gastrointestinal function
    o control of many stereotyped movements of the body
    o control of equilibrium
    o control of eye movements
    o way station for command signals from higher centers
A

Brainstem

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93
Q
  • activity of the neural circuitry within the spinal cord is modified and refined by descending motor control pathways
    o pyramidal tract
    ▪ CORTICOSPINAL TRACT
o	extrapyramidal tracts 
▪	RETICULOSPINAL TRACT
▪	VESTIBULOSPINAL TRACT
▪	RUBROSPINAL TRACT
▪	TECTOSPINAL TRACT
A

Descending Motor Control Pathways

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94
Q
  • influence mainly the muscles of the trunk and proximal parts of the limbs
  • important in maintenance of certain postures and in startle reactions
  • two main divisions
    o PONTINE or MEDIAL RETICULOSPINAL TRACT
    o MEDULLARY or LATERAL RETICULOSPINAL TRACT
A

Reticulospinal Tract

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95
Q
  • originates in the pontine reticular nuclei
  • projects to the ventromedial spinal cord
  • general stimulatory effect on both extensors and flexors, with the predominant effect on extensors
A

Pontine Reticulospinal Tract

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96
Q
  • originates in the medullary reticular formation
  • projects to spinal cord interneurons in the intermediate gray area
  • stimulation has a general inhibitory effect on both extensors and flexors, with the predominant effect on extensors
A

Medullary Reticulospinal Tract

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97
Q
  • originates in Deiters nucleus
  • projects to ipsilateral motoneurons and interneurons
  • important functions include:
    o control the activity of extensor muscles - stimulation causes a powerful stimulation of extensors and inhibition of flexors
    o maintenance of an erect posture - selectively controls the excitatory signals to the different antigravity muscles
    o making adjustments in response to signals from the vestibular apparatus
A

Vestibulospinal Tract

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98
Q
  • originates in the superior colliculus
  • projects to the cervical spinal cord
  • decussates before entry to spinal cord - lesions are always contralateral
  • important functions include
    o control of neck muscles
    o controlling head and eye movements
A

Tectospinal Tract

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99
Q
  • most important extrapyramidal tract
  • originates in the red nucleus
  • afferent information from cortex, cerebellum and basal ganglia
  • projects to interneurons in the lateral spinal cord
  • decussates before entry to spinal cord - lesions are always ipsilateral
  • controls both flexor and extensor muscles
    o stimulation of the red nucleus produces stimulation of flexors and inhibition of extensors
  • voluntary movements are impaired with lesions
A

Rubrospinal Tract

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100
Q

origin: Pontine reticular nuclei
projection: Ventromedial SC
decussation: None (ipsilateral)
function: Stimulate flexors and extensors

A

Pontine Reticulospinal tract

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101
Q

origin: Medullary reticular nuclei
projection: Intermediate gray
decussation: None
function: Inhibits flexors and extensors

A

Medullary Reticulospinal tract

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102
Q

origin: Deiters nucleus
projection: Ventromedial SC
decussation: None
function: Stimulates flexors and extensors

A

Vestibulospinal Tract

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103
Q

origin: Superior colliculus
projection: Cervical SC
decussation: Yes (Contralateral)
function: Controls neck muscles

A

Tectospinal Tract

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104
Q

origin: Red nucleus
projection: Lateral SC
decussation: Yes
function: Stimulates flexors, inhibits extensors

A

Rubrospinal Tract

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105
Q
  • involuntary flexion or extension of arms and legs
  • occurs when one set of muscles becomes incapacitated while the opposing set is not
  • indicates a severe medical emergency requiring immediate medical attention
  • two types:
    o DECORTICATE RIGIDITY
    o DECEREBRATE RIGIDITY
A

Abnormal Posturing

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106
Q
  • involuntary flexion of the upper extremities in response to external stimuli
  • arms flexed, hands are clenched into fists, legs extended and feet turned inward
  • less severe
A

Decorticate Rigidity

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107
Q
  • involuntary extension of the upper extremities in response to external stimuli
  • head is arched back, arms are extended by the sides, and legs are extended
A

Decerebrate Rigidity

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108
Q
  • cause decerebrate rigidity because of the removal of inhibition from higher centers
A

Lesions Above The Lateral Vestibular Nucleus

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109
Q
  • cause decerebrate rigidity because of the removal of central inhibition from the pontine reticular formation
A

Lesions Above The Pontine Reticular Formation But Below The Midbrain

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110
Q
  • result in decorticate rigidity and intact tonic neck reflexes
A

Lesions Above The Red Nucleus

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111
Q
  • also called the “little brain”
  • helps control the rate, range, force, and direction of movements (synergy)
    o sequences motor activities
    o monitors and makes corrective adjustments in motor activities while they are being executed
  • silent area of the brain
    o electrical excitation does not cause any sensation
    o damage does not produce paralysis
A

Cerebellum

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112
Q

Anatomy of the Cerebellum

A
  • located dorsal to the pons and medulla and protrudes from under the occipital lobes
  • divided into three lobes by two deep fissures
    o ANTERIOR, POSTERIOR, FLOCCULONODULAR
  • cerebellar cortex is actually a large folded sheet (17 x 120 cm) with crosswise folds (folia)
    o deep cerebellar nuclei lie deep beneath the folded mass of cerebellar cortex
    o from medial to lateral: DENTATE, EMBOLIFORM, GLOBOSE, FASTIGIAL
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113
Q

Brainstem Attachments

A
  • superior cerebellar peduncles to midbrain
  • middle cerebellar peduncles to pons
  • inferior cerebellar peduncles to medulla oblongata
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114
Q

Somatotopic Organization of the Cerebellum

A
  • vermis and intermediate zone contain a somatotopic map of the body surface
    o axial portions of the body lie in the vermis
    o limbs and facial regions lie in the intermediate zones
  • lateral portions of cerebellar hemispheres do not have topographical representations
    o receive input signals exclusively from cerebral cortex
    o plays important roles in planning and coordinating the body’s rapid sequential muscular activities
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115
Q

Layers of the Cerebellar Cortex

A

GRANULAR LAYER - innermost layer that contains granule cells, Golgi type II cells and glomeruli

PURKINJE CELL LAYER - middle layer that contains inhibitory Purkinje cells

MOLECULAR LAYER - outermost layer that contains stellate and basket cells, dendrites of Purkinje and Golgi type II cells and parallel fibers (axons of granule cells)

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116
Q
  • originate in the inferior olive
  • demonstrate complex spikes - action potentials beginning with a strong spike and followed by a trail of weakening secondary spikes
  • function in conditioning Purkinje cells (motor learning)
A

Climbing Fibers

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117
Q
  • form the bulk of the input, originating in the cortico-, vestibulo-, reticulo- and spinocerebellar tracts
  • demonstrate simple spikes - much weaker short-duration action potentials in Purkinje cells
A

Mossy Fibers

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118
Q
  • largest afferent projections

- originate from the basilar pontine nuclei

A

Pontocerebellar System

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119
Q
  • originate from the inferior olivary nuclei
A

Olivocerebellar Projections

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120
Q
  • originate in spinal cord or medulla
A

Spinocerebellar Fibers

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121
Q
  • originate from brainstem
A

Reticulocerebellar Fibers

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122
Q
  • originate from vestibular nuclei and vestibular apparatus
A

Vestibular Fibers

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123
Q
  • central neurons with fan-shaped dendritic trees

- always inhibitory with GABA as its neurotransmitter

A

Purkinje Cells

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124
Q
  • smallest and most numerous neurons in the brain
  • parallel fibers are axons of granule cells
  • excitatory input from mossy fibers which use glutamate as its neurotransmitter
A

Granule Cells

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125
Q

o small interneurons with numerous arborizations

o inhibitory in function

A

Golgi Type II Cells

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126
Q

o inhibitory star-shaped cells found in superficial cerebellum

A

Stellate Cells

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127
Q

o inhibitory cells whose axons form baskets around Purkinje fibers and are found in deep cerebellar layers

A

Basket Cells

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128
Q

o complex of synapses having a mossy fiber at its core

o synapsing with axons of Golgi type II neurons and dendrites of granule cells

A

Glomerulus

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129
Q
  • modulate Purkinje cell output
  • all of the cerebellar interneurons are inhibitory EXCEPT granule cells
    o granule cells have excitatory input to basket cells, stellate cells, Golgi II cells, and Purkinje cells
    o basket cells and stellate cells inhibit Purkinje cells (via parallel fibers)
    o Golgi II cells inhibit granule cells, thereby reducing their excitatory effect on Purkinje cells
A

Cerebellar Interneurons

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130
Q

Output of the Cerebellar Cortex

A
  • Purkinje cells are the only output of the cerebellar cortex
    o output is always inhibitory, using GABA as NT
  • inhibitory output modulates the output of the cerebellum and regulates rate, range, and direction of movement (synergy)
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131
Q

Efferent Signals from the Cerebellum

A

vermis - projects to fastigial nucleus, vestibular nucleus and reticular formation

intermediate zones - project to globose and emboliform nuclei (interposed nuclei)

lateral hemispheres - project to the dentate nucleus, ventral anterior thalamic nuclei and cerebral cortex

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132
Q

CEREBELLAR PATHWAY

A
Cortex
Pons* 
Cerebellum
Dentate nucleus*
Red Nucleus
Thalamus
Corticospinal tract
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133
Q

o consists of the small flocculonodular lobes

o for control of balance and eye movement

A

Vestibulocerebellum

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134
Q

o consists of lateral zones of cerebellar hemispheres

o for planning and initiation of movement

A

Cerebrocerebellum

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135
Q

o consists of vermis and intermediate zones

o for control of rate, force, range, and direction of movement (synergy)

A

Spinocerebellum

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136
Q
  • during nearly every movement, certain muscles must be rapidly turned on and then quick turned off
  • made possible by interplay of mossy and climbing fibers and Purkinje cells
A

Turn On/Turn Off Function

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137
Q

o climbing fibers modify sensitivity to parallel fiber input
o when mismatch between anticipated result of movement and its actual result occurs, climbing fiber input is more vigorous
o as movement is practiced, mismatch declines gradually

A

Motor Learning

138
Q

o during any movement, momentum develops and must be overcome to stop the movement
o appropriate learned, subconscious signals from spinocerebellum stop the movement precisely at the intended point

A

Damping Function

139
Q
  • patient with cerebellar lesion assumes unsteady stance and reeling gait (like a drunk person)
  • to compensate, he assumes a broad-based stance and a broad-based gait
A

Ataxia

140
Q
  • failure to meter the contractions that set the distance of motion
A

Dysmetria

141
Q
  • inability to perform rapid alternating movements
A

Dysdiadochokinesia

142
Q
  • failure of a movement to be terminated at a proper time
A

Past Pointing

143
Q
  • difficulty in maintaining position against sudden unexpected displacement
A

Overshooting

144
Q
  • slowness and slurring of speech
A

Dysarthria

145
Q
  • volume of voice varies from low to high from peak to peak
A

Scanning Speech

146
Q
  • tremor of intentionally maintained head or trunk posture or of a limb suspended in front of the body
A

Postural, Positional Or Static Tremor

147
Q
  • unsteady oscillations of the head or trunk
A

Tiutubation

148
Q

o tremor as a limb approaches its target

o results from cerebellar overshooting and failure of the cerebellar system to “damp” the motor movements

A

Intention, End-Point Or Kinetic Tremor

149
Q

-jerkiness of eye movement
o rapid, tremulous movements of the eyes rather than steady fixation
- due to failure of damping by the cerebellum
- occurs especially when the flocculonodular lobes of the cerebellum are damaged

A

Nystagmus

150
Q
  • decreased tone of the peripheral body musculature on the side of the cerebellar lesion
    o results from loss of cerebellar facilitation of the motor cortex and brain stem motor nuclei
  • shows rag doll appearance
A

Hypotonia

151
Q

o involves the anterior cerebellar lobe

o ataxia of the lower limbs only

A

Anterior (Rostral) Vermis Syndrome

152
Q

o involves the flocculonodular and posterior lobes

o axial ataxia without extremity ataxia

A

Posterior (Caudal) Vermis Syndrome

153
Q

o cerebellar signs lateralized to one half of the body

A

Cerebellar Hemisphere Syndrome

154
Q

o bilateral cerebellar signs due to involvement of all cerebellar lobes

A

Pancerebellar Syndrome

155
Q
  • deep cerebral nuclei involved in motor control
  • modulates thalamic outflow to the motor cortex to plan and execute smooth movements
  • demonstrates programming functions
    o generate basic patterns of movement in response to cues from cortical association areas
A

Basal Ganglia

156
Q

Role of Dopamine

A
  • connections between striatum and substantia nigra use dopamine as neurotransmitter
    o inhibitory on the indirect pathway (D2 receptors)
    o excitatory on the direct pathway (D1 receptors)
    o overall action is excitatory
157
Q

Important Functions of the Basal Ganglia

A
  1. Cognitive Control of Motor Activity

2. Timing and Scaling Functions

158
Q

o most of our motor actions occur as a consequence of thoughts generated in the mind
o major function of the caudate nucleus

A

Cognitive Control of Motor Activity

159
Q

o basal ganglia control the speed and size of movement
o posterior parietal cortex is the locus for spatial coordination
o projects heavily to caudate nucleus and explains why timing and scaling functions are lost with basal ganglia lesions

A

Timing and Scaling Functions

160
Q
  • snake-like or writhing movements of the hand and arm or face
  • result from lesions of the globus pallidus
A

Athetosis

161
Q
  • flailing movements of the extremities

- result from lesions to the sub thalamic nucleus

A

Hemiballismus

162
Q
  • brief, irregular, non-purposeful movements that are vaguely comparable to dancing
  • result from lesions to the corpus striatum (specially on caudate nucleus)
A

Chorea

163
Q
  • results from widespread destruction of the dopaminergic cells in the substantia nigra
  • characterized by:
    o cogwheel rigidity
    o resting pill-rolling tremor
    o slowness or difficulty in initiating movement (bradykinesia, akinesia)
    o postural instability (shuffling or fenestating gait)
A

Parkinson’s Disease

164
Q
  • autosomal dominant genetic disorder caused by CAG trinucleotide repeats
    o displays anticipation with succeeding generations
  • characterized by flicking movements in individual muscles (chorea)
    o leads to progressive severe distortional movements
  • caused by depletion of GABA and acetylcholine from many areas of the brain
A

Huntington’s Disease

165
Q

General vs. Special senses

A
General senses 
Somatic (Cutaneous) senses
- Touch, pressure, vibration, warmth, cold, pain, tickle, itch and proprioception
Visceral senses
- Stretch, pain, chemo-, osmotic-, baro-

Special senses
Olfaction, vision, taste, hearing and equilibrium

166
Q
  • comes from “Soma” or “Somato” - Greek word which means “body”
  • transmits information to the CNS about the state of the body and its contact with the environment
A

Somatosensory System

167
Q

Somatosensory system

A
Sensory receptor cells
        ↓
Neural pathways
        ↓
Brain cortex
168
Q
  • receive stimuli from the external or internal environment
  • Specialized epithelial cells
  • Neurons that transduce environmental signals (light, temperature) into neural signals
A

Sensory receptor cells

169
Q
  • conduct information from the receptors to the brain or spinal cord
A

Neural pathways

170
Q

deal primarily with processing the information

A

Brain cortex

171
Q
  • information processed by a sensory system may or may not lead to conscious awareness of the stimulus
A

Sensory information

172
Q
  • state of (conscious or unconscious) awareness of external and internal conditions in the body
A

Sensation

173
Q
  • conscious recognition of sensation
  • damaged neural networks may give faulty perceptions
  • Phantom limb: sensation of a limb that has been amputated
A

Perception

174
Q
  • onion-like structures surrounding unmyelinated nerve endings
  • found in deep skin layers
  • for vibration; tapping
A

Pacinian Corpuscle

175
Q
  • present in nonhairy skin; encapsulated in connective tissue
  • found in superficial skin layers
  • superficial touch (flutter and stroking movements)
A

Meissner’s corpuscle

176
Q
  • encapsulated enlarged nerve endings found in deep skin layers
  • for skin stretch
A

Ruffini’s Corpuscle

177
Q
  • found in superficial skin layers

- for steady pressure and texture

A

Merkel’s Disk

178
Q
  • found in muscles, joints, tendons

- for position

A

Propioceptors

179
Q

Thermoreceptors

A

Warm receptors - free nerve endings in skin for warm temperature (30-45C)

Cold receptors - free nerve endings found in skin for cold temperature (20-35C)

180
Q
  • free nerve endings found in skin, muscle and viscera for noxious stimuli and extreme temperatures
  • receptors for pain
A

Nociceptors

181
Q
  • Receptors are particularly distinct to a specific type of environmental change and less sensitive to other forms of stimuli
  • e.g. Vision receptors – contain pigment molecules that respond to light
A

Selective Response of Sensory Receptors

182
Q

Somatic sensation

A

Tactile sensations - Touch, pressure, vibration, tickle, itch
Themoreceptive sensation - Heat and cold
Pain
Proprioception - Receptors from this sensations comes from the skin, muscles, bones, tendons, and joints

183
Q
  • Mechanoreceptors with nerve endings linked to networks of collagen fibers within a capsule
  • Touch, movement, and vibration sensations - Rapid adapting receptors
  • Pressure - Slow adapting receptors
A

Touch-Pressure

184
Q
  • Muscle-spindle stretch receptors in skeletal muscles, mechanoreceptors in the joints, tendon organs (Golgi), ligaments, and skin
  • Also supported by vision and the vestibular organs
A

Posture and Movement

185
Q

Muscle spindle

  • Activity depends on muscle length
  • Annulospiral, flower-spray endings

Golgi tendon
- Passive stretch and active contraction increases the tension of the tendon that activate the tendon organ receptor

A

Stretch Receptors

186
Q
  • Sensitive to changes, not to absolute temperature
  • Adapt only between 20° and 40° C
  • Stimuli outside this range activate nocireceptors because of the high probability of tissue damage
  • Skin thermoreceptors play a role in temperature regulation, which is controlled by centers in hypothalamus
A

Temperature

187
Q
  • Gradiations of temperature: blue to red
    (freezing cold > cold > cool > indifferent > warm > hot
    > burning hot)
  • Cold spots > warm spots: located beneath the skin at discrete “spots”
  • Warm receptors- free nerve endings, transmitted thru type c fibers
  • Cold receptors- type A delta nerve fibers, some type c
A

Thermoreceptors

188
Q
  • free nerve endings that are stimulated when there is tissue damage
A

Pain: Nociceptors

189
Q

Qualities of Pain

A

Cutaneous pricking pain: well localized and easily tolerated
Burning pain: poorly localized and poorly tolerated
Deep pain: arising from the viscera, musculature and joints, poorly localized, can be chronic and often associated with referred pain

190
Q
  • Sensitive to a stimuli causing tissue injury
  • Chemical mediators include:
    Histamine, bradykinin & prostaglandins from site of injury
    ATP & 5-HT (serotonin) from platelets activated by injury
    Substance P from the primary sensory neurons
  • At 45°C, pain is perceived in the skin
A

Nociceptors

191
Q
  • Lactic acid accumulates in the tissues
  • Chemical agents formed
  • Perception of pain
A

Tissue ischemia

192
Q

Effect of mechanoreceptive pain receptors, ischemia

A

Muscle spasm

193
Q

Pain from deep structures of the head referred to the surface

Areas that are pain sensitive:

  • Venous sinuses
  • Tentorium
  • Dura at the brain base
  • Meningeal blood vessels
  • Middle meningeal artery
A

Headache

194
Q

Types of Intracranial headache

A
  • Headache of meningitis
  • Low CSF pressure headache
  • Migraine headache
  • Alcoholic headache
  • Headache cause by constipation
195
Q

Severe headache from the inflammation of meninges

A

Headache of meningitis

196
Q
  • Unknown mechanism
  • Starts with a prodrome lasting minutes to an hour

Theories of Migraine headache:

  • Vasospasm of the arteries producing ischemia
  • Spreading cortical depression
  • Psychological abnormalities
  • Vasospasm by excess potassium in the ECF
A

Migraine headache

197
Q

headache from absorbed toxic products or fluid loss in the gut

A

Headache caused by constipation

198
Q

headache due to Alcohol- toxic to tissues

A

Alcoholic headache

199
Q

Types of Extracranial headache

A
  • Headache from muscle spasm
  • Headache from irritation of nasal and accessory nasal structures
  • Headache caused by eye disorders
  • Muscle contraction
  • Excessive irradiation
200
Q
  • Pain of visceral origin is referred to sites on the skin and follows the dermatome rule
  • Sites are innervated by nerves that arise from the same segment of the spinal cord
  • E.g. ischemic heart pain is referred to the chest and shoulder
A

Referred Pain

201
Q

Causes of true visceral pain (poorly localized pain)

A
  • Ischemia of visceral tissue
  • Chemical damage to the visceral surface
  • Spasm of hollow viscus smooth muscle
  • Overdistention of hollow viscus
  • Stretching of tissues surrounding or within the viscera
202
Q
  • sharp, well localized pain
  • Visceral disease spreads to parietal peritoneum, pleura or pericardium
  • Parietal surface supplied with pain innervation – sharp pain
  • Appendicitis - Inflamed appendix pass pain impulses into the spinal cord levels T10 or T11 – referred pain to the umbilicus
A

Parietal Pain

203
Q

Sensory Transduction

A
Action potentials in nerve fibers
           ↑
Receptor potentials
           ↑
Transformation of stimulus energy
204
Q

Mechanisms of Receptor Potentials

A
  1. By mechanical deformation - Stretches the receptor membrane; Opens ion channels
  2. By application of a chemical - Opens ion channels
  3. By change of the temperature of the membrane
    - Alters the permeability of the membrane
205
Q
    • Central nerve fiber extending through its core.
    • Surrounding – multiple concentric capsule layers
  • -Compression anywhere on the outside of the corpuscle will Elongate, Indent or Deform the central fiber
    • Central fiber of the pacinian corpuscle
  • The tip of the central fiber - unmyelinated
  • The fiber - Myelinated
    • Sodium influx - a local circuit of current flow occurs
    • Node of Ranvier - action potentials are transmitted
A

Pacinian corpuscle: Eliciting an Action potential

206
Q
  • process by which an environmental stimulus activates a receptor and is converted to electrical energy
A

sensory transduction

207
Q
  • A single afferent neuron with all its receptor endings
A

Sensory unit

208
Q
  • area subserved by the sensory unit
  • overlap so that when 1 point is stimulated it activates several sensory units
  • E.g. ice cube on the skin give rise to sensations of touch and temperature simultaneously
  • Area of the body when stimulated, changes the firing rate of a sensory neuron
  • Large receptive field: less precise perception
  • Small receptive field: more precise perception
A

Receptive field

209
Q
  • Conversion of receptor potentials into action potentials that conveys sensory information to the CNS
  • Nature of a sensation and the type of reaction generated vary according to the destination of sensory impulses in the CNS
A

Sensory Coding

210
Q

Characteristics of the stimuli

A
  • Type (Modality)
  • Intensity
  • Location
  • Duration
211
Q
  • property by which one sensation is distinguished from another
    ModalitIes: Touch-pressure, Posture-movement, Temperature, Pain
    Submodalities: Warmth, cold (Temperature)

-The type of sensory receptor activated by a stimulus plays the primary role in coding the stimulus modality

A

Modality of sensation

212
Q

Frequency - Increased stimuli, increased action potential

Recruitment - “calling in” or activation of receptors on additional afferent neurons

A

Intensity of stimulation

213
Q

True or False

The more the receptor potential rises above the threshold level, the greater action potential frequency

A

True

214
Q
  • the magnitude of a subjective sensation increases proportional to a power of the stimulus intensity
  • the more power the stimulus gives you, the more sensation you feel
  • stimulus is directly proportional to sensation
A

Stevens’ power Law

215
Q
  • the magnitude of a subjective sensation increases proportional to the logarithm of the stimulus intensity
  • Very intense stimulation causes progressively less and less additional increase in amplitude of receptor potentials
  • Allows the receptors to have an extreme range of response
  • From very weak to very intense
  • ratio would matter and not the absolute weight
A

Weber-Fechner Law

216
Q

-Receptors adapt either partially or completely to any constant stimulus after a period of time.

When a continuous sensory stimulus is applied,

  • The receptor responds at a high impulse rate at first
  • Then progressively slower rate until
  • Finally the rate of action potentials decreases to very few to none at all
A

Adaptation of Receptors

217
Q
  • Muscle spindle; pressure; slow pain
  • Slowly adapting
  • Respond repetitively to a prolonged stimulus
  • Detect a steady stimulus
A

Adaptation: Tonic receptors

218
Q
  • Pacinian corpuscle; light touch
  • Rapidly adapting
  • Action potential frequency declines with time in response to a constant stimulus
  • Primarily detect onset and offset of a stimulus
A

Adaptation: Phasic receptors

219
Q
  • where the stimulus is being applied

- Acuity - precision in locating the stimulus; small receptive field size, more precise localization

A

Localization of stimuli

220
Q

receptors are at the edge of a stimulus is strongly inhibited compared to information from stimulus’ center

A

Lateral inhibition

221
Q
  • Transmit signals in varying frequencies
  • Diameter is proportional to conduction velocity
  • Labeled line principle
  • General and Sensory nerve classification
A

Sensory Nerve Fibers

222
Q

Nerve fibers are specific in transmitting only one modality of sensation

A

Labeled line principle

223
Q
  • Signals are subject to modification at the various synapses along the sensory pathways before they reach higher levels of the CNS
  • Information is reduced or even abolished by inhibition from collaterals from other ascending neurons (e.g., lateral inhibition) or by pathways descending from higher brain centers
A

Control of Incoming Sensory Signals

224
Q
  • Consists of a bundle of 3-afferent sensory neuron chains that run parallel to each other in the CNS and carry information to the cerebral cortex*
  • Specific ascending – carry a single type of stimulus
  • Nonspecific ascending – different stimuli
A

Ascending pathway (Sensory)

225
Q
  • Transmit information from somatic receptors pass the brainstem and thalamus into the Somatosensory cortex
  • Processing of afferent information does not end in the primary cortical receiving areas but continues to association areas of the cerebral cortex
A

Specific ascending pathway

226
Q
  • Polymodal neurons – different stimuli
  • Convey information from more than one type of sensory unit to the brainstem reticular formation and regions of the thalamus that are not part of the specific ascending pathways
A

Nonspecific ascending pathway

227
Q
  • Specific regions of the Primary Somatosensory area (postcentral gyrus, posterior to the central sulcus) receive somatic sensory input from different parts of the body
  • The major somatosensory areas of the cerebral cortex are SI and SII
A

Somatosensory cortex

228
Q

Sensory pathway: Receptors to the Cortex

A

First-order neurons
Second-order neurons
Third-order neurons
Fourth-order neurons

229
Q
  • Primary afferent neurons that receive the transduced signal and send the information to the CNS
  • Cell bodies are in the dorsal root or spinal cord ganglia
A

First-order neurons

230
Q
  • Located in the spinal cord or brain stem
  • Receive information from primary afferent neurons in relay nuclei and transmit it to the thalamus
  • Axons may cross the midline in a relay nucleus in the spinal cord before they ascend to the thalamus - sensory information originating on one side of the body ascends to the contralateral thalamus.
A

Second-order neurons

231
Q
  • located in the relay nuclei of the thalamus

- information ascends to the cerebral cortex

A

Third-order neurons

232
Q
  • located in the appropriate sensory area of the cerebral cortex
  • information received results in a conscious perception of the stimulus
A

Fourth-order neurons

233
Q
  • Ascending Anterolateral pathway/ Spinothalamic pathway
  • Dorsal column pathway
  • Pathways cross from the side where the afferent neurons enter the central nervous system to the opposite side either in the spinal cord (Anterolateral system) or in the brainstem (Dorsal column system)
A

Neural pathways of the Somatosensory system

234
Q
  • Fine touch, pressure, two-point discrimination, vibration, and proprioception
  • Consists primarily of group II fibers

Course:

  • Primary afferent neurons: cell bodies in the dorsal root, axons ascend ipsilaterally to the nucleus gracilis and nucleus cuneatus of the medulla
  • Second-order neurons cross the midline and ascend to the contralateral thalamus
  • Third-order neurons ascend to the somatosensory cortex, where they synapse on fourth-order neurons
A

Dorsal column system

235
Q
  • Temperature, pain, and light touch
  • Group III and IV fibers enter the spinal cord and terminate in the dorsal horn

Course:

  • Second-order neurons cross the midline to the anterolateral quadrant of the spinal cord and ascend to the contralateral thalamus
  • Third-order neurons ascend to the somatosensory cortex, where they synapse on fourth-order neurons
A

Anterolateral pathway

236
Q
  • Information from different parts of the body is arranged somatotropically
  • Destruction of the thalamic nuclei results in loss of sensation on the contralateral side of the body
A

Thalamus

237
Q
  • “Little man”
  • SI has a somatotopic representation similar to that in the thalamus
  • The largest areas represent the face, hands, and fingers, where precise localization is most important.
A

Sensory homunculus

238
Q
  • Fast pain

- Mechanical (intense pressure), thermal pain stimuli (>45° or

A

Neospinothalamic tract

239
Q
  • Touch sensations:
  • High degree of localization of stimulus.
  • Fine graduations in intensity of stimulus.
  • Phasic sensations (vibrations)
  • Sensations of movement against the skin.
  • Fine positional and pressure sensations
A

Dorsal Lemniscal System

240
Q
  • Thermal sensations: Cold, warm
  • Pain sensations
  • Crude pressure and touch sensations
  • Tickle and itch sensations
  • Sexual sensations
A

Anterolateral Spinothalamic System

241
Q
  • Slow pain
  • Polymodal nociceptors (high-intensity persisting mechanical, thermal or chemical stimuli)
  • C fiber (group IV)
  • Peripheral fibers terminate in the spinal cord almost entirely in laminae II and III of the dorsal horns, which together are called the substantia gelatinosa
  • Enters mainly lamina V, also in the dorsal horn
  • Join the fibers from the fast pain pathway, passing first through the anterior commissure to the opposite side of the cord, then upward to the brain in the anterolateral pathway
A

Paleospinothalamic tract

242
Q
  • Loss of sensation and motor function paralysis and ataxia caused by the lateral hemisection (cutting) of the spinal cord
  • Pain, temperature sensations lost on the opposite side of the body(Spinothalamic pathway)
  • Kinesthetic, position, vibration, discrete localization and two-point discrimination lost on the side of the transection (Dorsal column)
  • Crude touch retained
A

Brown Sequard syndrome

243
Q
  • Chronic disease of the spinal cord characterized by the presence of fluid-filled cavities and leading to spasticity and sensory disturbances
  • Generally in the cervical region, with resulting neurologic defects; thoracic scoliosis is often present
A

Syringomyelia

244
Q

Parenchymatous neurosyphilis marked by degeneration of the posterior columns and posterior roots and ganglion of the spinal cord

Manifestations

  • muscular incoordination
  • paroxysms of intense pain
  • visceral crises
  • disturbances of sensation
  • Trophic disturbances, especially of bones and joints(tabes-wasting)
A

Tabes dorsalis

245
Q
  • Selective suppression of pain without effects on consciousness or other sensations
  • Descending pathways selectively inhibit the transmission of information originating in nociceptors -> release certain endogenous opioids -> inhibit the propagation of input through the higher levels of the pain system e.g. morphine
A

Analgesia

246
Q
  • “Transmission” – turns on gate for pain
  • “Inhibitory” cells –shut the gate
  • Perception of pain is subject to modulation
A

Gating Theory of Pain modulation

247
Q

Analgesia system: Pain suppression in the brain and spinal cord

A
    • Periaqueductal gray and periventricular area of mesencephalon and upper pons
    • Raphe magnus nuclei, nucleus reticullaris pargigantocellular
    • Dorsal horn of SC – pain inhibitory complex
    • Stimulation of higher brain centers that suppress periaqueductal gray area can also suppress pain:
  • Periventricular nuclei in the hypothalamus
  • Medial forebrain bundle
    • Transmitters involved in the Analgesia system:
  • Enkephalin – presynaptic and postsynaptic inhibition of type Adelta and C fibers
  • Serotonin
248
Q
  • painful site itself or the nerves leading from it are stimulated by electrodes placed on the of the skin
  • stimulation of non-pain, low threshold afferent fibers (touch receptor fibers) leads to the inhibition of neurons in the pain pathways
A

Transcutaneous Electric Nerve Stimulation (TENS)

249
Q
  • Needles are introduced into specific parts of the body to stimulate afferent fibers, and this causes analgesia
  • Endogenous opioid neurotransmitters are involved in acupuncture analgesia
A

Acupuncture

250
Q

Analgesic drugs

A

Aspirin - inhibits the synthesis of prostaglandins and slows the transmission of pain signals from the site of injury

Opiates (endogenous opioids: endorphins & enkephalins) - act directly on opioid receptors in the brain, which activate descending pathways that inhibit incoming pain signals

251
Q

Sensory Pathways for Pain

A
  • Paleospinothalamic tract

- Neospinothalamic tract

252
Q

Most important Opiate-like substances - stimulate inhibitory neuron so that pain will be less

  • Met and leu-enkephalin
  • β-endorphin
  • Dynorphin
A

Opiate system

253
Q
  • portion of anterior end of diencephalon that lies below the hypothalamic sulcus and in front of the interpeduncular nuclei
  • divided into a variety of nuclei and nuclear areas
  • links the nervous system to the endocrine system via the pituitary gland
A

Hypothalamus

254
Q
  • portion of anterior end of diencephalon that lies below the hypothalamic sulcus and in front of the interpeduncular nuclei
  • divided into a variety of nuclei and nuclear areas
  • links the nervous system to the endocrine system via the pituitary gland
A

Hypothalamus

255
Q

Important Functions of the Hypothalamus

A
  • Endocrine Functions
  • Autonomic Functions
  • Limbic Functions
256
Q

___ hypothalamus increase BP and HR

A

posterior and lateral

257
Q

part of hypothalamus that decreases BP and HR

A

preoptic area

258
Q
  • hypothalamus controls the set-point of human body temperature
  • controlled by neurons in the preoptic area
  • signal appropriate cells to activate body temperature-lowering or temper-ature-elevating mechanisms
A

Body Temperature Regulation

259
Q

thirst center of the hypothalamus is the __

A

lateral hypothalamus

260
Q

__ release antidiuretic hormone (ADH) into posterior pituitary; controls urinary excretion of water; acts on cortical collecting duct of the kidneys to cause water reabsorption

A

magnocellular cells in supraoptic nuclei

261
Q

(hypothalamus)

___ release OXYTOCIN causes contraction of the smooth mus-cle of the uterus and milk let down

A

magnocellular cells in paraventricular nuclei

262
Q

(hypothalamus)

______ is responsible for hunger; lesions result in starvation; inhibited by leptin

A

lateral hypothalamus

263
Q

(hypothalamus)
___ is the satiety center; activity produces a “stop eating” signal; lesions cause uncontrolled voracious appetite; stimulated by leptin

A

ventromedial nucleus

264
Q

(hypothalamus)

__ are involved in reflexes related to food intake like lip licking and swallowing

A

mamillary nuclei

265
Q
  • hypothalamus elaborates releasing and inhibitory factors that modulate ante-rior pituitary function
  • subserved by periventricular zone, ar-cuate nucleus and ventromedial nucle-us
A

Anterior Pituitary Gland Regulation

266
Q

Hypothalamus is the __________ of autonomic nervous system; stimulation of the hypothalamus produces autonomic responses

A

head ganglion

267
Q

Autonomic Functions of the Hypothalamus

A

sympathetic: posterior hypothalamus - has a warming function
parasympathetic: anterior hypothalamus - has a cooling function

268
Q

• stimulation of hypothalamus affects behavioral control functions

A

Limbic Functions of the Hypothalamus

269
Q

__ hypothalamus causes increased general level of activity leading to rage and aggression

A

lateral

270
Q

(hypothalamus)

__ causes sense of tranquility, pleasure and reward

A

ventromedial nucleus

271
Q

(hypothalamus)

__ evokes fear and feelings of punishment and aversion

A

periventricular nuclei

272
Q

sexual arousal from __ of the hypo-thalamus

A

most anterior and most posterior portions

273
Q

o cycles of periodicity shorter than 24 hours

o examples: heart

A

Ultradian Rhythms

274
Q
  • cycles of periodicity longer than 24 hours

- examples: menstrual cycle, gestation

A

Infradian Rhythms

275
Q
  • cycles of periodicity that approximate Earth’s rotational period (24-hour day)
  • examples: sleep-wake cycle, hormone levels
A

Circardian Rhythms

276
Q
  • regulate activity of many physiological processes including heart rate, blood pressure, body core temperature and blood levels of hormones
  • external environmental clues influence strict 24-hour cycles
A

Biological Clock

277
Q

• implicated in regulation of circadian rhythms
• secretes a hormone called melatonin that is synthesized from serotonin
o increased during darkness
o inhibited by daylight
o controlled by sympathetic nerve activity, which is regulated by light signals from the retina

A

Pineal Gland

278
Q
  • also known as jet lag
  • physiological condition which results from altera-tions of circadian rhythms
  • when traveling across time zones, body clocks will be out of synchronization with the destination time - due to experience of daylight and darkness contrary to accustomed rhythms
  • treated with melatonin or sunlight exposure
A

Desynchronosis

279
Q

• unconsciousness from which the person can be aroused by sensory or other stimuli

A

Sleep

280
Q

Types of Sleep

A
  • Slow Wave Sleep / Non-REM Sleep

* Rapid Eye Movement (REM) Sleep

281
Q
  • deep, restful type of sleep
  • characterized by decreases in periph-eral vascular tone, blood pressure, respiratory rate and metabolic rate
  • frequently called dreamless sleep
  • however, dreams and sometimes even nightmares do occur during slow-wave sleep
A

Slow Wave Sleep / Non-REM Sleep

282
Q
  • called paradoxical because the brain is active and skeletal muscle contractions occur
  • lasts 5 to 30 minutes
  • repeats at 90 minute intervals
  • may be absent in extremely tired individuals
A

Rapid Eye Movement (REM) Sleep

283
Q

Important Characteristics of REM sleep

A

• active form of sleep associated with dreaming and active bodily muscle movements
• more difficult to arouse than slow-wave sleep
• muscle tone is exceedingly depressed
• irregular heart rate and respiratory rate (dream state)
• irregular muscle movements do occur
• brain is highly active in REM sleep
– overall brain metabolism increased by 20 percent
– EEG shows a pattern similar to wakefulness

284
Q

• raphe nuclei in lower pons and medulla - most conspicuous stimulation area for causing almost natural sleep
• nucleus of the tractus solitarius
• diencephalon
- rostral hypothalamus (suprachiasmal area)
- diffuse nuclei of thalamus

A

Sleep Centers: Slow-Wave Sleep

285
Q

What neurotransmitter is elaborated from raphe nuclei?

A

Serotonin

286
Q

Which Cranial Nerves arse subserved by the nucleus tractus solitarius?

A
  • Facial Nerve
  • Glossopharyngeal Nerve
  • Vagus Nerve
287
Q
  • drugs that mimic the action of acetylcholine increase the occurrence of REM sleep
  • gigantocellular cells
  • large acetylcholine-secreting neurons in the upper brain stem reticular formation
  • postulated sleep center for REM sleep
A

Sleep Centers: REM sleep

288
Q

Postulated Functions of Sleep

A
  • neural maturation
  • facilitation of learning or memory
  • cognition
  • conservation of metabolic energy
  • restoration of natural balance among neuronal centers
289
Q
  • measures voltage fluctuations resulting from ionic current flows within neurons
  • recording the brain’s spontaneous electrical activi-ty from multiple electrodes placed on the scalp
  • diagnostic applications: epilepsy, coma, brain death
A

Electroencephalography (EEG)

290
Q

Types of EEG Waves

A
  • Alpha Waves
  • Beta Waves
  • Theta Waves
  • Delta Waves
291
Q
  • rhythmical waves with a frequency of 8-12 Hz at about 50 mV
  • found in normal, awake but resting (eyes closed) individuals
  • disappear during deep sleep
A

Alpha Waves

292
Q
  • occur at frequencies of 14 to 80 Hz with voltage less than 50 mV
  • recorded mainly from parietal and frontal regions
  • occur when the eyes are opened in the light
  • requires intact thalamocortical projections and ascending reticular input to thalamus
A

Beta Waves

293
Q
  • wave frequencies of 4 to 7 Hz
  • occur mainly in the parietal and tem-poral areas in children but may appear in adults during emotional stress
  • associated with brain disorders and de-generative brain states
A

Theta Waves

294
Q
  • all of the waves below 3.5 Hz
  • occur during deep sleep, organic brain disease and in infants
  • persist in the absence of cortical input from the thalamus and lower brain centers
A

Delta Waves

295
Q
  • fairly regular pattern of waves at a frequency of 8–13 Hz and amplitude of 50–100 V (alpha waves)
  • most marked in the parietal and occipital lobes
  • associated with decreased levels of attention
A

Alpha Rhythm

296
Q
  • alpha rhythm is replaced by an irregular 13–30 Hz low-voltage activity (beta waves)
  • also called alpha block, arousal response or desynchronization
  • produced by any form of sensory stimulation or mental concentration
A

Beta Rhythm

297
Q
  • lapsing abruptly into REM sleep from awake state
  • sleep episodes last about 15 minutes without warning
  • often triggered by a pleasurable event
  • emotionally intense experience can also trigger cataplexy, a sudden loss of voluntary muscle control
A

Narcolepsy

298
Q
  • sleepwalkers arise from slow wave sleep in a state of low consciousness and perform activities that are usually performed during full consciousness
  • little or no memory of the incident, as they are not truly conscious
A

Somnambulism / Sleep Walking

299
Q
  • chronic inability to obtain the amount or quality of sleep needed to function adequately during the day
  • most common cause is psychological disturbance
A

Insomnia

300
Q
  • temporary cessation of breathing during sleep
  • loss of muscle tone during sleep allows excess fatty tissue or other structural abnormalities to block the upper air-way
  • associated with obesity and made worse by alcohol
A

Sleep Apnea

301
Q

• entire neuronal circuitry that controls emotional behavior and motivational drives
• important communicating structures:
- brain stem via the medial forebrain bundle
- hippocampus to mammilary bodies via fornix

A

Limbic System

302
Q
  • first pathway hypothesized to explain appreciation and expression of emotion
  • responsible for linking the experience and the expression of emotion
  • cingulate cortex is the seat of emotional experience
  • output from the cingulate cortex is conveyed via the fornix to the hypothalamus, where it is trans-lated into the expression of emotion through the autonomic nervous system
A

Papez Circuit

303
Q

Functions of Limbic System

A
5 F’s
Fighting
Fleeing
Feeding
Feeling
Fucking/Fornicating
304
Q
  • stimulation evokes rage, passivity and excessive sexual drive
  • highly hyper excitable - weak stimuli can cause seizures
  • lesions cause ANTEROGRADE AMNESIA (inability to form new memories)
  • provides signals for consolidation of memory
A

Hippocampus

305
Q

• window of the limbic system
- receives neuronal signals from all portions of the limbic cortex, as well as from the neocortex of the temporal, parietal, and occipital lobes

• functions

  • endocrine and vegetative functions
  • involuntary movements
  • rage, escape, punishment, severe pain and fear
  • sexual activity
A

Amygdala

306
Q
  • results from bilateral destruction of the amygdala
  • manifestations include
    o hyperorality
    o loss of fear
    o decreased aggressiveness
    o changes in eating behavior
    o psychic blindness
    o excessive sexual drive
A

Kluver Bucy Syndrome

307
Q
  • most poorly understood portion of the limbic system

* cerebral association area for control of behavior

A

Limbic Cortex

308
Q

(Limbic Cortex)

lesions in the bilateral anterior temporal cortex will cause __

A

Kluver-Bucy syndrome

309
Q

(Limbic Cortex)

lesion in bilateral posterior orbitofrontal cortex will cause __

A

insomnia, restlessness

310
Q

(Limbic Cortex)

lesion in bilateral anterior cingulate and subcallosal gyri will cause __

A

extreme rage reaction

311
Q

• acquisition of the information that gives an organism the ability to alter behavior on the basis of ex-perience
• two types:
o ASSOCIATIVE LEARNING
o NON-ASSOCIATIVE LEARNING

A

Learning

312
Q
  • also called simple learning
  • modification of response to a repeated stimulus
  • habituation occurs when the response be-comes weaker as the stimulus is perceived to have no particular importance
  • sensitization occurs when the response is en-hanced in the even that an unpleasant or otherwise strong stimulus is given
A

Non-Associative Learning

313
Q

• involves the ability to make a connection between a neutral stimulus and a second stimulus that is ei-ther rewarding or noxious
• two important examples:
o CLASSICAL CONDITIONING
o OPERANT CONDITIONING

A

Associative Learning

314
Q

is a learning process in which behavior is sensitive to, or controlled by its consequences

A

Operant Conditioning

315
Q

is a learning process in which an innate response to a potent stimulus comes to be elicited in response to a previously neutral stimulus; this is achieved by repeated pairings of the neutral stimulus with the potent stimulus

A

Classical Conditioning

316
Q

• ability to store, retain and recall information and past experiences
• two types:
o EXPLICIT / DECLARATIVE MEMORY
o IMPLICIT / NONDECLARATIVE MEMORY

A

Memory

317
Q

▪ associated with consciousness (conscious attention)
▪ dependent on the hippocampus and other parts of the medial temporal lobes
▪ depends on higher-level thinking skills such as influence, comparison, and evaluation
▪ memories can be reported verbally

A

Explicit/ Declarative Memory

318
Q

▪ does not involve awareness
▪ retention does not usually involve processing in the hippocampus
▪ acquired slowly through repetition
▪ includes motor skills and rules and procedures
▪ procedural memories can be demonstrated

A

Implicit/ Nondeclarative/ Reflexive Memory

319
Q
  • stored in the brain by changing the basic sensitivity of synaptic transmission between neurons as a result of previous neural activity
  • new or facilitated pathways are called memory traces
A

Physiology of Memory

320
Q
  • lasts seconds to hours

- memory traces are subject to disruption by trauma and various drugs

A

Short-Term Memory

321
Q
  • form of short-term memory that keeps information available, usually for very short periods
A

Working Memory

322
Q
  • stores memories for years and sometimes for life

- long-term memory traces are remarkably resistant to disruption

A

Long-Term Memory

323
Q

What type of neuronal circuit is exemplified in short-term memory?

A

Reverberating Circuit

324
Q
  • initiation of chemical, physical, and anatomical changes in the synapses
  • rehearsal enhances the transference of short-term memory into long-term memory
  • new memories are codified into different classes of information
  • postulated to be a function of the HIPPOCAMPUS
A

Consolidation of Memory

325
Q

Physiologic Evidences of Long Term Memory

A
  • increase in vesicle release sites for secretion of transmitter substance
  • increase in number of transmitter vesicles released
  • increase in number of presynaptic terminals
  • changes in structures of the dendritic spines that permit transmission of stronger signals
326
Q

• condition in which memory is disturbed or lost
• two basic types:
o ANTEROGRADE
o RETROGRADE

A

Amnesia

327
Q
  • loss of short-term memory
  • impairment of the ability to form new memories through memorization
  • usually caused by bilateral lesions to the HIPPOCAMPUS
A

Anterograde Amnesia

328
Q
  • loss of pre-existing memories to conscious recollection
  • person may be able to memorize new things but is unable to recall events or identity prior to the on-set
  • usually result from lesions to the THALAMUS
A

Retrograde Amnesia

329
Q
  • right hemisphere is dominant in facial expression, intonation, body language, and spatial tasks
  • left hemisphere is dominant with respect to language, even in left-handed people
  • information is transferred between the two hemi-spheres through the CORPUS CALLOSUM
A

Hemispheric Specialization

330
Q
  • human communication is distinguished by its range and subtlety of expression
  • vocalization is the production of sound that has no specific meaning
  • language consists of a specific vocabulary and a set of rules of expression (syntax)
A

Language

331
Q
  • located in the inferior frontal lobe of the dominant hemisphere
  • processes the information received from Wernicke’s area into a detailed and coordinated pattern for vocalization
A

Broca’s Area (Brodmann Area 44)

332
Q
  • located in posterior superior temporal gyrus of the dominant hemisphere
  • concerned with comprehension of auditory and visual information
A

Wernicke’s Area (Brodmann Area 22)

333
Q
  • bundle of the nerve fibers that connect Wernicke’s area to Broca’s area
A

Arcuate Fasciculus

334
Q
  • appears to process information from words that are read in such a way that they can be converted into the audito-ry forms of the words in Wernicke’s ar-ea
A

Angular Gyrus (Brodmann Area 39)

335
Q
  • abnormalities of language functions that are not due to defects of vision or hearing or to motor pa-ralysis
  • caused by lesions in the categorical/dominant hemisphere
  • most common cause is Cerebrovascular Disease
A

Aphasia

336
Q

Types of Aphasia

A
  • Broca’s Aphasia
  • Wernicke’s Aphasia
  • Conduction Aphasia
  • Anomic Aphasia
  • Global Aphasia
337
Q
  • lesion in Broca’s area
  • also called non-fluent aphasia or expressive aphasia
  • speech is slow and words are hard to come by
  • patients with severe damage to this area are limited to two or three words
A

Broca’s Aphasia

338
Q
  • lesion in Wernicke’s area
  • also called fluent aphasia or receptive aphasia
  • speech is normal
  • patients talk excessively (jargon, neologisms)
  • fails to comprehend the meaning
A

Wernicke’s Aphasia

339
Q
  • lesion in ARCUATE FASCICULUS
  • patients can speak relatively well and have good auditory comprehension but cannot put parts of words together or conjure up words
A

Conduction Aphasia

340
Q
  • lesion in ANGULAR GYRUS (written words)
  • no difficulty with speech or the understanding of auditory information
  • trouble understanding written language or pictures
  • visual information is not processed and transmitted to Wernicke’s area
A

Anomic Aphasia

341
Q
  • due to generalized brain destruction
  • more than one form of aphasia is often present
  • speech is scant as well as nonfluent
A

Global Aphasia