• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/54

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

54 Cards in this Set

  • Front
  • Back
43 AD-scribonius largus
electric torpedo ray to treat headache/gout
peripheral nerves
1755 AD- Le Roy
wires around blind man head
-results= pain & flashes of light!!
1804 AD- Aldini
-building on galvani animal electricity
-put electricity on parietal bone of person suffering melancholia (depression type) =improved mood
1960's applied electricity to animal brain!
weak___currents to cortex=
current weaker than needed for causing
showed that
problem
-DC, spont activity and evoked resonses for hours in rat
-AP's
-sub threshold current can change neural excitability
-brain under scalp/skull= high electrical resistance
faradays electromagnetic induction
pass current thru coil=current in opposite direction of second coil and generate magnetic field when vary the EF
magnetic fields good because (2)
pass thru almost unaltered thru scalp/skull
minimally invasive stimulation
1896 d arsonval
1910 thompson
show get ___if stimulate with coil
phosphenes
based on stimulating retina
also possible to stimulate thru visual cortex
TMS by
Barker in 1985
76: focused peripheral nerve stimulators
82: improved design
85:tms
principles of tms (6)
-current in coil
-magnetic field pulse
change of magnetic field rat
induce electric field
induce tissue current
induce charge density
electocompulsive therapy
not same as tms
used for depression very effective BUT very invasive
*tms may be able to do same thing but would be better not there yet
is tms non invasive
it excites__neurons
is low or high tech
2 effects overtly measured
yes
cortical
low
muscle twitches& if stimulate visual system to see flashes light (non random position of coil will affect where see flashes)
what affects tms stimulation efficiency
-hardware ( risetime, intensity, coil shape and size)
-neural anatomy (orientation/length/beding angle, distance from coil, resistance, brain size)
tms
spatial resolution=
temporal=
good at/pros
.5cm
50ms
modulating brain activity
minimally invasive
**if it disrupts task performance then disrupted area is essential to (not just correlated) to task performance
cons of tms
-not useful without priori info (need to know where we're going to stimulate with tms, ie any type of mapping needs other techniques mostly fMRI &/or ERP
-only stimulate surface structures
-safety concerns
can you stimulate deeper with tms
yes but affect/stimulate other ares along the way
why use mri instead of tms
see structural lesions/damage
discover areas involved in cognitive processes
study role of any brain structure
map structural connections
why use tms instead mri
-if area is crucially involved
-better at mapping functional connectivity
-induce plasticity
-measure intracortical inhibition/facilitation
discuss flowchart of how its used/applied
-intervention/modulating: rTMS (therapeutic or basic research) or time course single pulse
-monitoring: use single or paired pulse
single pulse tms good to use on people after rehab training after stroke because
it porbes corticomotor pathway
describe single pulse tms and corticomotor probing
-pulse over primary motor cortex
-attach electrode to hand-->measure muscle activity creates Motor Evoked Potential from CONTRALATERAL hand
-look at MEP's latency&luitude (2 good diagnostic tools for stroke/multiple sclerosis
TMS intensity for motor/visual target
-use motor threshold
find stimulation--> twitch
look at amp's in emg
take the middle value
*visible? subjective? EMG?
-use visual threshold (flashes of light)
TMS intensity for NOT motor/visual target
relative threshold approach
ex) MT (motor threshold) 61% so lets go above it like 80% and see what happens
w/ TMS how do you know where you're stimulating
-with muscle its easy, stimulate areas until one spot gives best muscle response
-if not muscle, use other techniques ex) BRAINSIGHT --> functional mri, can use as overlay w/ tms
after pulse happens have 2 main effects
-sync neurons activity
-sync--> gaba IPSP's (this also helped us learned about gaba function) lasts 50-250ms
TMS=cortical
inhibition
-pulse pinches muscle= MEP (spike you see) then have silent/dead period= cortical silent period
cortical silent period is____in stroke patients and can inhibit many other functions
prolonged
next slides discuss paired pulse
..
paired pulse
-little tiny pulse doesnt cause effect itself BUT effects brain--> tiny pulse if given for ex) 1ms before high intensity pulse the MEP of high intensity GONE!!!
-around 6-8 the MEP of high pulse comes back
-little pulse influencing brain response to high pulse
-as interval time increase MEP of second pulse increases * at 10-15 ms see facilitation
w/ paired pulse learned that
-gaba chemical promote the inhibitory aspects
-glutamate promotes the facilitation
ie) can indirectly measure ratio of inhibitory and excitatory neurochemicals in brain
sICI
short-interval intracortical inhibition
sICI and silent period measures of _____and operate thru____mechanisms
inhibition
different
**sICI uses gaba A-R
**silent period uses gaba B-R
lisa koski looking at multiple sclerosis (MS) and sICI cSP whats one thing she found
-those with increased inhibition were performing better on some tasks
-maybe due to adjustment in NT levels/excitability that determines how the damage will be manifested by disabilties
tms safety concerns
-cant do on
pregnant
metal in head
history of seizure
taking TCA/ drugs change neural excitabilty
pacemaker
-can give you
headache (main complaint, more do to constraint on head/sitting there for long time)
hearing loss (inconsistent data, just give earplugs)
look at intervention: time course single pulse
...
used by amassian
showed suppresion of______by tms stimulation of
visual percpetion
occipital cortex
*this study showed TMS as mapping tool
describe amassian study
-flash letters and ask you to say ones you saw
-at intervals combined tms single pulse with flashing letter
-smaller the interval the less likely to see certain letters, show time interval that optimal for info to properly reach area/process info
-also could promote seeing some letters better like the letter farthest right
*reminder: stimulation lead to inhibition of visual perception
rTMS
-repetitive tms
-varying freq of pulses
-longer lasting effects!!
-summation of neurophysiological effects
rTMS:
2 type of study design
online= stimulation SAME time as task performed
**all online is excitatory
offline= stimulation then perform task
**1 Hz vs 10Hz applies only to offline
1Hz vs 10Hz
1Hz: suppresses neural excitability
10 Hz: enhances neural excitability
safety issues with rTMS;
similar to single/simple tms
increased chance of seizure
risk defined by intensity, freq, number trains
international workshop on safety of rTMS= define safety parameters
phineas gage example of__lesion
real
damage to ant frontal lobe
virtual lesions
temporary
use virtual lesion to study
area MT--> visual motion perception
PFC--> hand selection in rxn time
SMA--> performance of over learned sequential finger movement
temporal cortex--> free recall of verbal material
*SKY IS THE LIMIT THEORETICALLY (at least at surface)
wada test
-inject sodium amobarbital into internal carotid artery
-ask patient name images
-determines laterality function
can rTMS be used for wada
potential there, some shown
-rTMS over brocas area (high intensity/freq) showed similar results to wada
first tms lab in canada by
paus
Paus:
describe experiment looking at rTMS & PET
-10 Hz rTMS over right frontal eye field
-5 pulses/train
-# trains, 5, 10, 15, 20,25, 30
-brain regions show inc/dec in uptake/metabolism based on # trains
-some regions connected to areas that were stimulated also became stimulated
**first ever demonstration of effective connectivity without behavioral confound
rTMS as therapeutic used on stroke patients discuss study
-10 Hz on lesions/damaged hemi= increased excitability (not as high as unlesioned)
-also gave 1Hz on unlesioned/normal hemi= decrease in excitabilty of unlesioned hemi BUT increased excitability on lesioned hemi ie) maybe the unlesioned excitabilty has dampening effect on lesioned
rTMS in humans vs animals
-humans
high freq= LTP
low freq=LTD
-animals
LTP/LTD needs longer stimulation/higher frew therefore use THETA burst pulse
TBS
-intermittent or use continuous
-much faster procedure
-3 50Hz pulses repeated every 200ms
given either:
intermittent or continuous
would we get better results with theta burst pulse if used in humans
-for inhibitory
cTBS effect last longer than rTMS
BUT effect same size
-for facilitation
no difference between iTBS and rTMS
non fluent aphasia:
lesion that include__area result from
identified by
brocas ;middle cerebral artery infarts
agrammatism in speech/writing
giving rTMS to non fluent aphasics=
long term benefits
supports idea that increased contralateral activity not compensatory
potential therapeutic option
rTMS also possible therapy for
depression
symtoms on Ham D scale decrease with rTMS