Lecture 4 Flashcards

1
Q

What are neuroanatomical techniques?

A
•  The day-to–day of biopsychologists
•  “Seeing the forest for the trees”
•  General approaches vs specific approaches
•  Selecting level analysis 
–  Molecular
–  Structural/anatomical 
–  Functional
•  More detail not always beer
–  Neurons tightly packed
•  Differences in resolution
•  Total understanding can result only from convergence of studies at all levels
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2
Q

What are neural stains?

A
•  Selective
–  Stain some Mssue components
and not others
    •  Nucleus, ribosomes, cell membrane
•  Preparing brain tissue –  Perfusion
    •  Remove blood 
–  Hardening
    •  Freezing or paraffin embedding 
–  Slicing
    •  Microtome
–  Mounting
    •  Albumen
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3
Q

What are golgi stains?

A
•  Silver chromate stained neurons black
•  Not all neurons pick up stain
•  No intracellular details
•  Shapes and sized of neurons
•  First view of synapse
–  Cajal, Nobel Prize, Neuron Doctrine
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4
Q

What are missile stains?

A
•  Penetrates all cells
•  Stains ribosomes
•  Soma visible
– Can better quantify (esMmate)
number of cells
•  First view of structures within neuron
•  Cresyl violet
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5
Q

What are electron microscopy?

A

• Greater magnification than light microscope
– Electrons are smaller particles of light
• Slices coated with electron- absorbing substance (gold)
– Different parts of neurons absorb gold to different degrees
• Electron beam passes through slice and image captured
• Minutecellulardetails
– difficult to assess overall or general structure
• Scanning EM generates 3D images

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6
Q

What is tracing neural pathways?

A

• Identify pathways that connect structures
– Axon staining
• Anterograde tracing
– Where do axons go?
– Autoradiography
• Amino acids with radioactive hydrogen isotopes are taken into cell bodies and incorporated into proteins
• Wait for a few days and identify radioactivity in axon terminals
• Retrograde tracing
– Where do axons come from
– HRP taken up by axon terminals
– Wait a few days
– Brain stained with HRP substrate to change it to black
• Black identifies originated cell bodies

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7
Q

What are contrast x-rays?

A

• Effective only if internal structures differ from their surroundings
– Differences in X-ray absorption
• Brain too many overlapping structures absorbing Xrays to same degree
– To stand out: radioopaque material into structure of interest
– Discovered by Moniz
• X-ray passed through brain onto photographic plate
• Angiography
– Dye injected into carotid artery
• Reveals enlarged or displaced blood
vessels
• Pneumoencephalography
– Air injected into CSF
• Identify enlarged and displaced ventricles

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8
Q

What are x-ray computed tomography (CT)?

A

• Early 1970s
• Computer assisted Xray
• 3-d view of brain
• Brain CT composed of 8-9 horizontal secMons
• Xray gun and detector rotate in apposiMon around head
• Not sharp image
– Low resoluMon axial image
• Used to visualize structural abnormalities: – Tumors
– Stroke damage
– Concussion/brain injury

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9
Q

What is a positron emission tomography (PET)?

A

• Highlight metabolically active brain areas
• Inject carotid artery with positron emiong radionuclide (eg. 2-deoxyglucose)
– 2-dg structurally similar to glucose and active cells take up more glucose
– 2dg can’t be metabolized so it accumulates in active cells
• Positrons interact with electrons, produce photons (gamma rays)
• Scanner detects photons and how many gamma rays coming from particular region
• Indicates areas of acMvity during task (reading, speaking, remembering, etc.)
– No temporal resolution
• Axial images
• No structural informaMon
– Poor spatial resolution
– Coregistered with MRI
• Can also identify non activity measures
– Neurotransmitters
– Receptors
– Transporters
– Ions

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10
Q

What are magnetic resonance imaging (MRI)?

A

• High spatial resolution
• Horizontal, coronal and sagiRal planes
• Expensive $$$
• No ferrous metal
• Strong magneMc field passed through brain
– Aligns hydrogen atoms
– Rf pulse causes hydrogen atoms to
emit electromagnetic frequency
• Scanner detects emitted radiation
– Neural structures differ greatly in hydrogen atom density

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11
Q

What is an fMRI?

A

• Most influential tool in cog neuro
• Uses MRI methods
– Functional
– Structural
– Non invasive
• No injection
– 3D images of activity over brain
– High spatial resolution
– Poor temporal resolution; better than PET
• 2-6 sec delay
– AP msec
• BOLD response: Activity related-changes in blood flow
– Oxygenated blood accumulates in active areas
• Oxy and deoxy hemoglobin different magnetic moments
– Detect changes in blood oxygenation
• Hemodynamics
• Warning: pictures do not reflect changes in activity, they reflect changes in BOLD signal

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12
Q

What is diffusion tensor imaging (DTO)?

A

• Identify white matter tracts in brain
– Connections among structures
– Human “connectome” project
• Use MRI technology
• Water molecules move in same direction in white matter
– Outside of white matter water molecules diffuse randomly
• Example DTI findings:
– Alcohol degrades white matter
– Pre clinical AD deterioraMon of white matter

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13
Q

What is transcranial magnetic stimulation (TMS)?

A

• Disrupts neural activity by placing magnetic field under coil positioned over skull
– during cognitive and behavioural tasks
– Assess functions of different cortical areas
• Establish structure-function
• PET and fMRI correlate activity to task
• TDCS
– Apply current directly to scalp
• Noninvasive
• Intervention
– Mixed results
• Current quesMons: – Depth of effect
– Safety
– Exact mechanism of neural disruption

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