studying the brain Flashcards
problem with light microscope
light defracted when it hits objects, one dot can look like a whole distribution because of wave like tendencies of light
therefore we cant see anything smaller than the wavelength of light
how do we overcome light microscope problems?
laser to eliminating samples, find the centre of light creating a more defined image
switch on molecules separately, they dont overlap
spatial resolution
how fine detail we can see
temporal resolution
seeing things happen
patch clamp electrode tip
tiny tube that can be brought dow on surface of neurons, measure change in voltage
electroencephalogram (EEG)
on scalp to give sum of electrical activity
neurons align -> dipole b/c align -> results
global info (doesn’t tell where)
- bad temporal res???
CT / CAT SCAN
fire x ray all around then subtract to see
spatial image ONLY
(is there a bleed?)
PET SCAN
gamma rays
inject brain with glucose, neurons fight off positrons letting off gamma rays which are detected
accumulate where there is more activity
stim - ctrl= diff
MRI
(T1 vs T2)
radio waves
high spatial info -> structural
T1 weighted: high detail
T2 weighted: map of H2O density (ions in water) -> tumours are inflammatory and show in T2
FMRI
functional
activated regions have more oxygen
shows oxygenated vs deoxy
low temporal resolution
MR tractography
measures water concentration in brain