1/2: Neuroscience Review - O'Connell Flashcards

1
Q

Define lower motor neuron lesion; descibe symptoms

A

lower motor neuron = alpha motor neuron; located in anterior horn of spinal cord and cranial n. nuclei; innervate skeletal muscle fibers.

Symptoms = weak or paralyzed muscles. Decreased or absent muscle stretch reflexes. Flaccid weakness. Profound atrophy, fasciculations, fibrillations.

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2
Q

Define upper motor neuron lesion; descibe symptoms

A

immediate = spinal shock induced hypotonia and flaccid paralysis.
With time = spastic paralysis. Increased muscle stretch reflexes. Clonus. Babinski/extensor plantar resposne. Larger areas of body.

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3
Q

pt has an ischemic stroke involving the RIGHT ANTERIOR cerebral artery - what part of the body is affected? What if left? What if right/ left mddle cerebral a. ?

A

right anterior cerebral a. correlates with left genitalia, thigh and feet. Middle cerebral a. correlates with fingers, face, arm (everything else)

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4
Q

Match sensory fiber size/type with function

A

Ia = afferent muscle spindle
Ib = golgi tendon organ afferent
group I = Aalpha

Group II = Abeta
Group II = axons of encapsulated endings

Group III = Adelta
Group III = responsible for sharp fast pain

Group IV = C fibers.
Group C = burning slow pain.

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5
Q

which fiber is responsible for fast pain? For propioception?

A

fast pain = group III/Adelta

large sensory fibers (group I/II responsible for propioception (and fine tactile sensations, two point discrimination and vibratory sensation.)

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6
Q

Describe the role of enkephalin interneurons in nociceptive sensory tranmission. Which areas of the nervous system excite the enkephalin interneurons?

A

release from interneurons of enkephalins that inhibit the flow of pain information to the brain.

enkephalins (and dynorphin) are found in the periaqueductal gray, the medulla and the dorsal horns

“natural opiod”

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7
Q

fasciculation

A

a brief, spontaneous contraction affecting a small number of muscle fibers, often causing a flicker of movement under the skin.
It can be a symptom of disease of the motor neurons

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8
Q

fibrillation

A

a small, local, involuntary, muscular contraction, due to spontaneous activation of single muscle cells or muscle fibers.

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9
Q

motor neuron pool

A

all motor neurons innervating a muscle

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10
Q

motor unit

A

a motor neuron and all the muscle fibers it innervates

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11
Q

paraplegia v. quadriplegia

A

transection of spinal cord below cervical level but above lumbar enalrgement
high cervical level lesion

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12
Q

ataxia; cerebellar ataxia; sensory ataxia

A

failure of muscular coordination, defective muscular control resulting in irregular and jerky movements

ataxia due to lesion in the cerebellum itself

ataxia due to damage to the sensory input to the cerebellum

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13
Q

intention tremor v. resting tremor

A

resting associated with Parkinsons

intention associated with Cerebellar issues

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14
Q

lead pipe rigidity and cogwheel rigidity

A

Leadpipe rigidity results when an increase in muscle tone causes a sustained resistance to passive movement throughout the whole range of motion, with no fluctuations.

Cogwheel rigidity is a combination of lead-pipe rigidity and tremor which presents as a jerky resistance to passive movement as muscles tense and relax

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15
Q

bradykinesia

A

slowness in execution of movement

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16
Q

akinesia

A

lack of movement

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17
Q

dysdiadochokinesia

A

inability to perform rapid alternating movements -

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18
Q

dysmetria and hypermetria

A

errors in range and force of movements

voluntary muscular movement over reaches the intended goal

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19
Q

chorea

A

involuntary movment; brief sudden random twitch “dance like”

20
Q

dystonia

A

neurological movement disorder in which sustained muscle contractions cause twisting and repetitive movements or abnormal posture

21
Q

atheotosis

A

a condition in which abnormal muscle contractions cause involuntary writhing movements

It affects some people with cerebral palsy, impairing speech and use of the hands.

22
Q

describe the lesion responsible for parkinsons and give characteristic signs of disease

A

Degeneration of dopaminergic projection to striatum from substantia nigra

Observe: tremor at rest, rigidity, slowing of movement and postural instability.

23
Q

describe lesion responsible for huntigton’s disease and give characteristic signs of disease

A

Selective loss of GABA/enkephalin projection from striatum to globus pallidus
Later more sidespread degeneration of striatal neurons.

Observe: chorea, dementia, bradykinesia.

24
Q

damage to r. dorsal column =

A

loss of propioception, discriminative touch and vibratory sense in right foot

25
Q

damage to somatosensory area of r. thalamus would cause?

A

loss of dorsal colum mediated sensation in l. foot

26
Q

damage to posterior limb of internal capsule OR to the somatosensory cortex?

A

contralateral deficits in dorsal column mediated sensations

27
Q

stereognosis and grphestesia are lost ___ to a lesion of the somatosensory cortex, thalamus, or medial lemniscus

A

contralateral - these higher functions are lost ipsilateral to a dorsal column lesion

28
Q

nociceptive information from the viscer is carried in..

A

dorsal columns

29
Q

system responsible for carrying nociceptive and thermoceptive signals from Ad and C fibers

A

anterolateral system - also includes information from mechanoreceptors with large receptor fields (crude touch)

30
Q

midline lesion of the spinal cord (ex: early syringomyelia) cause?. To pain and temp sensation

A

bilateral loss of pain and temperature at the level of the lesion
spinal cord lesions of just one side of the cord cause contralateral loss of pain and temp sensation

31
Q

brown-sequard syndrome **

A

hemisection of spinal cord = loss of dorsal column sensations ipsilateral to lesion and pain and thermal sensation contralateral to the lesion

32
Q

a brainstem lesion above the medulla causes?

A

deficits of all somatosensory modalities contralateral to the lesion; posterior internal capsule and cerebal cortex lesion also cause contralateral deficits

33
Q

describe parietal neglect syndrome

A

usually result of lesion to non-dominant hemisphere; since language usually in l. hemisphere, lesion of right hemisphere can cause left-sided neglect

34
Q

presynaptic problem with NMJ might be? postsynaptic might be?

A
botulism
myasthenia gravis (autoimmune with antibodies against nicotinic Ach receptors)
35
Q

lesions of large areas of motor cortex can cause?.

A

upper motor neuron lesion symptoms contralateral to the lesion

36
Q

lesions of the spinal cord can cause?

A

upper motor neuron symptoms for ipsilateral muscles innervated by neurons below the level of the lesion

37
Q

effects of lesions in the vestibulocerebellum

A

distrubances of equilibrium and eye movemet control (smooth pursuit), ataxic gait

38
Q

effects of lesion in the spinocerebellum

A

IPSIALTERAL problems in control of leg movmeents persist when pt is supine

39
Q

symptoms are ___ to cerebellar lesions

A

ipsilateral

40
Q

only problems raising one corner of mouth vs. problems with eye and mouth.

A

upper motor neuron defect : contralateral defect in lower face. . Lower motor neuron lesion: ipsilateral defects.

41
Q

effect of lesion of corticospinal tract

A

lose fine control of digits. Cannot perform individual movements of the digits

42
Q

brain stem lesion?

A

LMN cranial n. signs on side of lesion, UMN signs are seen on contralateral body

43
Q

ataxic gait falls?

A

toward side of cerebellar lesion

44
Q

causes intention tremor

A

dysmetria

45
Q

principle signs of cerebellum dysfunction

A
ataxic gait
nystagmus
dysmetria (intention tremor)
 dysdiadochokineasia
decomposition of movement