Lecture 9- Measuring neural activity II Flashcards
How do you use genetically encoded Ca indicators? (GCaMPs)
-can use it to image a whole network of neurons in the gut wall -genetically engineer a mouse, where all cells expressing a protein can be made to a GCaMP (Ca indicator) -cross of a mouse expressing Cri and GCaMP3 -GCaMP3 is in all neural crest derivatives -so indicator only expressed in the cells controlling the gut -activation of nicotinic acetylcholine receptors
What is the resolution like with genetically encoded Ca indicators?
-high spatial width of field, low temporal resolution -calcium signal lasts a very long time -as Ca handling not happening instantaneously= slower than AP, the start of Ca means neuron is active but the decay of Ca is slow = in terms of resolution= indication when things start= spatial resolution high but temporal bad!
Are there equivalents of the GCaMPs for the brain?
-similar version for the brain as well= another inidcator that is event better -opening skull and exposing to virus so they have the indicator= then look at activity of neurons through the window of the skull, requires genetic engineering and much equipment -can record from a number of neural cells
What is at the other end of the spectrum?
-psychophysics -we’ve been talking about single cells, this is about the whole system
What is the classic visual brightness illusion and what does it tell us about the nervous system?
-which rectangle is the brightest -this is the psychopsychotic recording: -A) identical, the black background makes one look much lighter B) the same issue = this tells us about how the visual system work, on/off, our brain adjust our ability to determine colour in contrast to background -using this trick can work out how the system actually processes information -eyes detect green/red, blue/yellow, separately • Can use this and other illusions to study visual pathways via brain imaging • Psychophysics and other psychological tests need to be rigorous and well controlled
What is the first element of psychophysics?
-structural imaging of brain
What are the characteristics of an MRI (Magnetic Resonance Imaging)
-structural magnetic resonance imaging -very common, non-invasive -nucleus has characteristic response in a strong magnetic field and when it is changed, method that has been around for at least 50 years -recently= if computing plus tomography= can do MRI= depends upon having a huge magnet= shifting the magnetic field and measuring the consequences= can get beautiful images of particular regions, grey matter= lighter, white matter= darker -can tell if there is a disturbance= tumour (white) -the green, red etc= activity (from fMRI)
What is the resolution like in an MRI?
-very good spatial resolution and extremely poor temporal resolution
What are the types of dynamic brain imaging?
-fMRI -PET -• Both assume that increased blood flow reflects increased neural activity – Inherently limits time resolution -dynamic= where you look at the change in the brain during a function of some kind
What are the characteristics of fMRI?
– Usual form measures changes in blood oxygen levels (BOLD) – Also various forms of MR spectroscopy – Reasonable spatial resolution, but requires many repetitions – Used together with structural MRI -fMRI= if you repeat a stimulus and scan eventually can see the activity -instead of tuning to the mag. resonance to detect water (MRI) they detect BOLD (fMRI)
What are the characteristics of PET?
– Simplest form measures blood flow – Low spatial resolution -PET= inject radioactive marker, often tecticium (half life 90 mins),it is giving out the positron= flies a certain distance from a nucleus then hits electron= anihilation= 2 gamma rays going in opposite direction, from that you can tell where the positron was emitted Positron emission tomography= can label individual neurotransmitters etc. -300 different ligands that can be studied this way -the amount of radiation is tiny and not a health risk
What is an example of fMRI usage (odours)?
- fMRI of active regions to different odours
- allows you to see a key feature of the technique: same individual exposed to pleasant vs unpleasant odour -different pattern of activation
- the white circled= not related to odour per say, it has a role in the pleasantness
- pink= region lights up in both cases so must be connected to odour itself
- problems= the test subject must tell you they detect the signal= must move or something, must have output to the experimenter and that will have parts of the brain light up
What is the resolution like for fMRI and PET?
• Low spatial resolution and often poor temporal resolution
What are fMRI and PET good for and often used for?
• Good for non-invasive studies of locations of specific functions • Both used to localise brain regions associated with specific behaviours
Is fMRI and PET resolution improving?
• Resolution of fMRI is improving, but theoretical limits make it difficult to identify basic mechanisms • PET can be used to study binding sites for drugs and transmitters, but inherent limitations in spatial resolution limit its utility -both BOLD and PET= depend on the idea when neural activity increases then blood to that region increases, increase in BOLD= is the overcompensation for the loss of oxygen when active -these are delayed from the actual neural activity -limit to temporal resolution -nor fMRI or PET cannot replace single unit recordings etc. in terms of resolution temporally and spatial as well but can scan the whole brain -with PET= need cyclotron under the PET scan as the radioactive material decays very quickly