neuroscience Exam 1 Flashcards

1
Q

what is the fundamental neuronal process that underlies all aspects to brain function?

A

electrical signaling

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2
Q

what are dendrites?

A

branchlike extensions
receive info from other neurons

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3
Q

which way do afferent neurons travel?

A

away from body, toward CNS

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4
Q

which way do efferent neurons travel?

A

to body, away from CNS

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5
Q

what is an axon?

A

output unit of the cell
arises from axon hillock
has nodes of ranvier

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6
Q

what is a synapse?

A

sites of communication

presynaptic: finger like projections
synaptic cleft: space between neurons
postsynaptic:

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7
Q

what is axoplasmic transport?

A

mechanism that transports substances along an axon
anterograde: down first
retrograde: back up second

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8
Q

what does axonal transport appear slow?

A

aging
neurodegenerative diseases

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9
Q

how is information transmitted through a neuron?

A

synapse > dendrite > cell body > axon > synapse

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10
Q

what are bipolar neurons?

A

something on each end of cell body - dendritic root and axon

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11
Q

what are pseudounipolar cells?

A

peripheral and central axons
cell body is over on the side

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12
Q

what are multipolar cells?

A

have multiple dendrites arising from cell body
most common in body

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13
Q

what substances are higher in ECF?

A

sodium
chlorine

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14
Q

what substance is higher in ICF?

A

potassium

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15
Q

what are modality gated channels?

A

open in response to mechanical forces

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16
Q

what are ligand gated channels?

A

open in response to neurotransmitter binding

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17
Q

what are voltage gated channels?

A

open in response to changes in electrical potential

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18
Q

what are leak channels?

A

small number of ions leak at slow continuous rate

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19
Q

what is resting membrane potential?

A

value of electrical potential when at steady state
leak channels and Na+/K+ pump

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20
Q

what is the value on the inside of the neuron?

A

-70 to -90

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21
Q

what does the Na/K pump move?

A

2K in and 3Na out with each cycle

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22
Q

define depolarized

A

less negative than RMP
excitatory

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23
Q

define hyperpolarized

A

more neg than RMP
inhibitory

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24
Q

what is local potential?

A

at receiving sites
1-2mm - very small area
if stimulus is larger and longer, potential will be larger and longer lasting

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25
Q

temporal summation

A

changes occur within milliseconds

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26
Q

spatial summation

A

generated in different regions and added together

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27
Q

when is an action potential generated?

A

depolarizes beyond voltage threshold
all or nothing
longer distances

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28
Q

step to an action potential

A

RMP
depolarizing stim
voltage gated Na channels open
rapid Na entry depolarizes
Na close and K open
K moves from cell to ECF
K leaves cell and hyperpolarizes the cell
voltage gated K close
return to RMP

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29
Q

what is the refractory period?

A

channels become inactivated after opening AP

absolute: cannot be stimmed
relative: if greater depol current, can be stimmed

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30
Q

propagation of AP

A

increased diameter of axon increases speed
faster when thicker sheath

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31
Q

what are the functions of myelination?

A

insulation
prevents leakages
increases the speed

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32
Q

what are nodes of ranvier?

A

lack of myelin
high densities of Na and K channels

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33
Q

what is saltatory conduction?

A

quick node to node jumping

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34
Q

what are glia?

A

form a support network for neurons

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35
Q

describe astrocytes

A

star shaped
grey matter
role in cell signaling
maintain nutrition and blood supply of cell bodies
clean up debris
form scars

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36
Q

what are oligodendrites and schwann cells?

A

form myelin sheath
white matter

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37
Q

what is the difference between oligodendrites and schwann cells?

A

olig - CNS
schwann - PNS

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38
Q

what are microglial cells?

A

immune system of CNS
clean up and remove debris

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39
Q

what are glial stem cells?

A

immature and undifferentiated cells
can do whatever you need

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40
Q

what is neuroinflam mediated by?

A

reactive microglia and astrocytes

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41
Q

what are the beneficial effects of neuroinflam?

A

when reactive microglia clean up and remove debris

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42
Q

what are the harmful effects of neuroinflam?

A

excessive activation
death of neurons

correlation between abnormal glial activity and neurla damage in stroke

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43
Q

what does damaged myelination do?

A

slow and impede conduction of AP

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44
Q

what is multiple sclerosis?

A

damage to myelin sheath in brain and SC
autoimmune disorder
diagnosis is difficult

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45
Q

what are the S&S of MS?

A

lack of coordination and balance
impaired vision
double vision
impaired sensation
paresis/paralysis
speech difficulties
spasticity
increased reflexes
gait difficulties

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46
Q

what is the first symptom for 20% of MS pts?

A

visual symptoms

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47
Q

what is the symptom that 80% of MS pts have?

A

visual
double vision is most common

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48
Q

what is relapsing/remitting MS?

A

most common type
alternate between relapses/remissions
without treatment, most transition to secondary progressive

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49
Q

what is secondary progressive MS?

A

continuous decline with few or no relapses

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50
Q

what is primary progressive MS?

A

steady functional decline from time of onset
10%

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51
Q

what is progressive relapsing MS?

A

steady functional decline with relapse/partial remissions
function never fully recovers in remissions
5%

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52
Q

what is a synapse?

A

where a neuron and a post synaptic terminal meet

majority are chemical

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53
Q

where can synaptic communications between neurons ocur?

A

cell body - axosomatic
dendrites - axodendritic
axon - axoaxonic

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54
Q

sequence of events in synaptic transmission

A

transmitter synthesized and stored in vesicles
AP invades presyn terminal
depol of presyn terminal causes opening of Ca channels
influx of Ca through channels
Ca causes vesicles to fuse with presyn membrane
transmitter released into syn cleft via exocytosis
transmitter binds to recepter molecules in postsyn membrane
opening or closing of postsyn channels
postsyn current causes excitatory or inhibitory postsyn potential that changes the excitability of postsyn cell
removal of neurotransmitter by glial uptake or enzymatic degradation
retrieval of vesicular membrane from plasma membrane
transmitter is synthesized and then stored in vesicles

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55
Q

what opens the voltage gated ca channels?

A

depol of presyn membrane

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56
Q

what is needed for vesicle fusion and transmitter release?

A

influx of Ca

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57
Q

what are the different messages that depend on amount of neurotransmitter released?

A

reuptake of neurotransmitters
degradation of NT by enzymes
diffusion of NT
change in structure of membrane receptors

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58
Q

what happens if NT is not cleaned out?

A

overflow
stop binding
leads to MG

59
Q

what potential happens from local depol?

A

excitatory postsynaptic potential

60
Q

what potential happens form a local hyperpol?

A

inhibitory postsynaptic potential

61
Q

when is AP triggered?

A

only if overall summation is sufficient to depol the cell to thresholdd

62
Q

where is NT released?

A

synaptic cleft

63
Q

where are neuromodulators released?

64
Q

which NT/NM are excitatory?

A

ACh
glutamate
dopamine
norepi
substance P
nitric oxide

65
Q

which NT/NM are inhibitory?

A

GABA
glycine
dopamine
histamine
norepi
endorphins
enkephalins

66
Q

what is an agonist?

A

mimic effects naturally occuring NTs

67
Q

what is an antogonist?

A

prevent the release of NT or bind to impede the effects

68
Q

describe ACh

A

excitatory at all NMJ
initiation of skeletal muscle contraction
myasthenia gravis
botox inhibits ACh
parasympathetic
slows heart rate
increased smooth mus contractions
constriction of pupil

69
Q

describe norepi

A

sympathetic
increase HR
dilation of bronchioles
control of mood
agonists are amphetamines and cocaine
excessive: fearful, panic disorder, PTSD

70
Q

describe dopamine

A

pleasure
behaviors reinforcement
decision making
planning
parkinson’s: inadequate levels in caudate and puta
drugs for park can induce involuntary mvmts

71
Q

describe serotonin

A

throughout gray matter
reg of sleep, appetite, arousal, mood
low levels associated with depression and anxiety
SRIs allow sero to stay in receptor longer
high levels asso with OCD and schizo

72
Q

describe GABA

A

sedation
antianxiety
antiseizure
sleep inducing
benzos enhance GABA
epilepsy meds can decrease excessive neural activity

73
Q

describe glutamate

A

learning and memory
excessive can cause seizures
too much destroys neurons

74
Q

describe endorphins

A

inhibition of pain signaling

75
Q

describe substance P

A

sensation of pain
released by nerve endings
res and CV control
mood reg
signals interpreted as pain

76
Q

describe lambert-eaton syndrome

A

autoimmune
antibodies destroy voltage gate Ca channels
ACh cannot be released
decreased release of NT

77
Q

describe myasthenia gravis

A

attack and destroy ACh receptors on muscle cells
there is still normal release of ACh
affect NMJ
males 60-70, females 20-30

78
Q

what are the clinical features of MG?

A

repetitive use of muscles leads to increased weakness
usually affects eye movements (drooping)
facial expressions
proximal limb weakness
swallowing
difficulty speaking
weakness of breathing muscles

relieved with rest

79
Q

WEAKNESS in regards to MG

A

weakness of neck, face, eyes, arms, legs
eyelid drooping (ptosis)
appearance (not a lot of expressions)
keep chocking and gagging while eating
no energy
extraocular muscle weakness, diplopia
slurred speech, hoarse voice
shortness of breath

80
Q

treatment of MG

A

drugs that inhibit breakdown of ACh
removal of thymus gland
immunosuppressants
plasmapheresis

81
Q

what is channelopathy?

A

dysfunction of ion channels
genetic mutation
can happen at any channel that affects AP

82
Q

how is MS diagnosed?

A

it is difficult
usually manifests with one sign that can completely resolve

83
Q

what gait disturbances are common in MS?

A

asymmetric step lengths
reduced speed
scissoring gait
ataxic gait
increased fall risk
fear of falling
decreased ability to dual-task

84
Q

how is MS managed?

A

medication to modify the process or slow attacks
plasmapheresis
PT and OT
avoid high temps and stress

85
Q

describe the somatic nervous system

A

voluntary, under conscious control
innervates skeletal muscle
consist of single motor neuron

86
Q

describe autonomic nervous system

A

involuntary
controls and modulates functions primarily of visceral organs
consist of 2 neurons pathway: preganglionic and post

87
Q

what does ans regulate?

A

homeostasis
circulation
respiration
digestion
metabolism
secretions
body temp

88
Q

what are the efferents of the ANS?

A

sympathetic - fight or flight - thoracolumbar
parasympathetic - rest or digest - brainstem and sacrum

89
Q

what do adrenergic neurons do?

A

release norepi
receptors for norepi are called adrenoreceptors

90
Q

what do cholinergic neurons do?

A

release ACh
receptors for ACh are called cholinoreceptros

91
Q

which neurons are cholinergic?

A

all preganglionic
some postganglionic

92
Q

which neurons are adrenergic?

A

some postgang

93
Q

what is the function and role of sympathetic nervous system?

A

mobilize body for activity
maintain blood supply to organs

94
Q

fight or flight extremes of symp

A

increased arterial pressure
incr blood flow to active muscles
incr metabolic rate
incr blood glucose concentration
incr HR and contractility
incr mental activity and alertness
incr ventilation
decr GI motility: decr blood flow, peristalsis and secretions

95
Q

what is the function of parasympathetic nervous system?

A

restorative, to conserve energy

96
Q

where do pregang neurons arise?

A

CN 3, 7, 9, 10 or from S2-4

97
Q

pupillary constriction and dilation

A

parasym stim of circular mus - contraction
sym stim of radial mus - dilation

98
Q

para/sym in relation to near/far sight

A

para - focus near, round lens
sym - focus far, flat lens

99
Q

what are mechanoreceptors?

A

respond to mechanical deformation

100
Q

chemoreceptors

A

respond to chemicals released by cells

101
Q

thermoreceptors

A

respond to heat/cold

102
Q

nociceptors

A

sensitive to stimuli that damage to threaten damage
sensation of pain

103
Q

describe receptive fields

A

area of skin innervation by single afferent neuron
small distally, larger proximally

test: two point touch, min distance that feel two points

104
Q

1a and II axons

A

proprioception
muscle spindle
thickest mye

105
Q

AB

A

touch
merkel, meissner, pacinian, ruffini cells
second thickest mye

106
Q

Adelta

A

pain, temp
free nerve endings
thinnest mye

107
Q

C axons

A

pain, temp, itch
free nerve endings
unmye

108
Q

conscious relay pathways

A

location and type of stim
accurate details about stim and location
aware of it

109
Q

divergent pathways

A

info from many locations in brainstem and cerebrum
both conscious and uncon

110
Q

unconscious relay pathways

A

proprioceptive info
role in autonomic adjustments of mvmts and posture

111
Q

first order neuron

A

has cell body in post root ganglion
conveys to medulla

112
Q

second order neuron

A

fibers enter spinal cord to synapse with it
medulla to thalamus

113
Q

third order neuron

A

synapses with it in thalamus
axons ascend to higher level
thalamus to cerebral cortex

114
Q

DCML

A

touch
proprio

115
Q

anterolateral/spinothalamic

A

pain
temp
crude touch

116
Q

deep sensations

A

joint position sense
mvmt awareness
vibration

117
Q

superficial sensations

A

pain
temp
light touch
pressure

118
Q

combined cortical sensations

A

2 point discrimination
barognosis - weight discrimination
graphesthesia -
tactile localization
texture recognition
stereognosis

119
Q

dorsal column sensations

A

discrim touch
proprio
vibration
2 point
bargonosis
graphesthesia
texture recog
sterognosis

120
Q

fasciculus gracilis (medial)

A

axons from lower limb and lower trunk
cross in lower medulla
into lumbar spine

121
Q

fasciculus cuneatus (lateral)

A

axons from upper limb and upper trunk
cross in lower medulla
into cervical spine

122
Q

trigeminal lemniscus

A

from face directly to pons
cross in pons

123
Q

anterolateral column axons transmit what?

A

pain (free nerve endings, nociceptors)
temp
crude touch

124
Q

what are some different AL column pathways

A

spinothalamic - ant: crude touch, lat: pain and temp
spinolimbic - limbic lobe - emotions
spinoreticular - reticular formation
spinomesencephalic - midbrain

125
Q

spinothalamic pathway: how many order neurons?

A

3 order neurons

primary: bring info to dorsal horn of SC
secondary: cross midline and project to thalamus
tertiary: from thalamus to cerebral cortex

126
Q

what is crossed analgesia

A

once everything is crossed, contralateral effects
absence of pain in response to stimuli that normally would be painful

127
Q

what is fast pain?

A

early perception of sharp pain
inital and immediate
A delta fibers

128
Q

what is slow pain?

A

duller, bright quality
following sharp pain
dull throbbing, burning ache, not well localized
C fibers, unmye

129
Q

describe the medial pain system

A

many responses to nociception
affective, motivation, arousal, withdrawl, autonomic
uses several pathways, not 3 order
cannot be accurately localized

130
Q

spinomesencephalic tract

A

periaqueductal gray
superior colliculus
descending pain control system
turning eyes and head to source of noxious input

131
Q

spinoreticular tract

A

ascending neurons
modulates arousal, attention, sleep-waking cycles
sever pain needs attention and interferes with sleep

132
Q

spinolimbic tract

A

transmit slow pain into to medial and intralaminar nuclei in thalmus
axons project to anterior cingulate cortex, insula, amygdala
interferes with thinking, behavior, and social activities

133
Q

unconscious relay tracts to cerebrum

A

info from proprio is transmitted to cerebrum via spinocerebellar tract

posterior spinocerebellar pathway - lower half of body
cuneocerebellar - upper half of body
anterior spinocerebellar - thorcolumbar SC
rostrospinocerebellar - cervical cord

info not consciously perceived
for uncon adjustments to mvmt and posture

134
Q

considerations for sensory exam

A

“are there any areas of your skin where your feeling has changed or decreased?”
“does the skin on one side feel different than the other?”
explain the test you will do, show the pt what you will do, allow pt to feel the stimulation that will be applied
define the terms “sharp” and “dull”
vision should be eliminated

135
Q

touch awareness and tactile localization

A

have pt tell you when and where they feel it
testing DCML

136
Q

testing sharp/dull

A

tests lateral spinothalamic system
use paperclip
ask “is this sharp or dull”

137
Q

temperature testing

A

warm water (40 C), cold water (10 C)
maintain contact with skin for 3 seconds before asking for a response

138
Q

tactile threshold (pressure)

A

“say yes if you feel the touch”
apply filament at 90 deg with enough force to make it bend

WNL: 2.83 (5g force)

139
Q

joint mvmt/position testing

A

“tell me whether i am moving/have positioned your joint up or down”

140
Q

vibration testing

A

use tuning fork
“is it vibrating?”
can only be tested on bones

141
Q

testing bilateral simultaneous touch

A

“tell me which side is being touched”

142
Q

graphesthesia

A

“tell me what letter i draw on the palm of your hand”
testing DCML

143
Q

sterognosis

A

“tell me what this is”
“you can move it around in your hand”