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79 Cards in this Set
- Front
- Back
What is Neurogenesis, and what's one chemical often used in it?
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cell proliferation & cell creation;
beta catenin |
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Cell Differentiation
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development of a cellular phenotype
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Cell Migration
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movement of cells to their final locations
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Pathseeking
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creation of connections, aka neurite outgrowth, synapse formation
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What is Apoptosis?
What causes it? |
programmed cell death, caused by lack of neurotrohpic factors
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What do Caspases do, and how do they work?
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cause cell death by cleaving (cutting peptide bonds) on proteins at the carboxy-terminals of amino acids connecting to the amino acid aspartate
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Beta Catenin
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an example of a protein that stimulates cell division in stem cells; NEUROGENESIS
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Reelin
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a chemical telling cells to stop migrating
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Where does Adult Neurogenesis occur?
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*hippocampus
*olfactory bulb *perhaps in other areas |
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Achaete-scute Proteins
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let a cell become a support cell
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bHLH Transcription Factors
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let cell become a neuronal precursor
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CNTF in glial development leads to...
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leads to astrocytes
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PDGF in glial development leads to...
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leads to oligodendrocytes
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Radial Glial Cells
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An early appearing glial cell (Radial Glia) is also attached to the ventricular surface and pial surface.
SCAFFOLDING IN THE EPENDYMAL LAYER |
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Inside out Development of the Neocortex: explain!
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Cells created early in development occupy the lowest layer of the cortex, those that develop late in development are found at the surface.
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Neurotrophic Factor: explain
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if target cell number was increased a greater number of presynaptic cells survived. The chemicals released from target cells that have these properties are called Neurotrophic Factors – peptides.
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Neurotrophins: example, and function
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Are neurotrophic factors
examples: NGF, BDNF, Neurotropin 3, Neurotrophin 4 |
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Tyrosine Kinase Receptors (trk A, B, C); what are they and how do they work?
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All receptors for neurotrophic factors are tyrosine kinase receptors; the activation of which, in a similar fashion to G protein activation, stimulates second messenger pathways and regulates gene transcription
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Cadherins, Laminin
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examples of chemoaffinity chemicals found in the extracellular fluids
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Semaphorins, Netrin
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examples of chemoaffinity chemicals found on cell surfaces
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Cones
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color-sensitive receptors in eyes
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Rods
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non-color sensitive receptors in eyes
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Retinal Ganglia Cells
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axons which form the optic nerve
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Lateral Geniculate Nucleus has 6 layers. Which are ipsalateral; which are contralateral?
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ipsalateral: 1, 4, 6
contralateral: 2, 3, 5 |
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Area V1 (Striate Cortex):
Where is it, and what else is it called? |
in occipital lobe; = Primary visual cortex = Calcarine cortex
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Principles behind experienced induced alternation of visual circuitry
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Hebbian:
FIRE TOGETHER WIRE TOGETHER OUT OF SYNC LOSE YOUR LINK |
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What is the significance of the ependymal layer in development?
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It's where stem cells are.
The nervous system originates from stem cells (ependymal cells) -Undifferentiated, multipotential cells- found along the edge of the ventricular spaces – ventricular zone or the EPENDYMAL LAYER – of the brain. |
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Neural plate
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End of 3rd week: group of medially placed cells appear dorsally in the ectoderm.
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Neural groove
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Soon after its formation the neural plate folds inward at the midline and cells proliferate laterally.
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Neural tube
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As the lateral areas grow they move upward and eventually merge together at the top to form neural tube
FORERUNNER OF BRAIN'S VENTRICULAR SYSTEM |
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What are Delta and Notch?
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DELTA: ligand
NOTCH: receptor Initially, all cells in “proneural” areas of the fruit fly express delta and notch in equal amounts, then, minor differences in the initial levels of delta in one cell induces a cascade that will cause one cell to become a nerve cell and its neighbors to become glia or some other kind of support cell. Enhanced delta activity in one cell activates the notch receptor in an adjacent cell which then inhibits the second cell’s ability to make delta. |
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Occular Dominance Columns: where are they?
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Layer IV of Area V1 / Striate Cortex
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Occular Dominance Columns: how were they discovered?
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Hubel and Wiesel injected radioactive stuff into eye --> radioactive areas are the occular dominance columns
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Occular Dominance Columns: how do they develop?
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ODCs don’t exist at birth; Layer 4 responds to both eyes
Over time, diff. regions of the brain begin to specialize; become responsive to input from only one eye (Tested via monocular visual deprivation on animals) At 2 weeks, eye goes to entire layer 4 At 13 weeks, ODCs are really really large for open eye |
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Cranial Nerve 1:
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Olfactory. Smell.
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Cranial Nerve 2:
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Optic. Eyes.
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Cranial Nerve 3:
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Ocularmotor. Ocular motor.
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Cranial Nerve 4:
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Trochlear. Ocular motor.
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Cranial Nerve 6:
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Abducen. Ocular motor.
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Cranial Nerve 8:
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Vestibulocochlear; audio and balance
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Cranial Nerve 10:
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Vagus: major nerve of vPNS
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The Rhinencephalon is in the _______ and is responsible for ______.
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Forebrain
olfactory/smell |
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The Limbic Cortex is in the _______ and contains ______, _____, _____.
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Forebrain
amygdala, hippocampus, cingulate cortex |
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The amygdala is in the ______, and is responsible for ______.
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Limbic cortex
emotion |
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The hippocampus is in the ________
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limbic cortex
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Cingulate cortex: PLACE, FUNCTION
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LIMBIC CORTEX
attention/self monitoring, feelings |
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Thalamus: P/C
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3rd ventricle / diencephalon; forebrain
LGN/MGN |
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Hypothalamus: P/F
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3rd ventricle / diencephalon; forebrain
Pituitary |
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Tectum contains:
Tectum is in: |
Superior and inferior colliculi
Midbrain |
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Superior colliculus: P/F
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Tectum; vision [motor/sensory]
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Inferior colliculus: P/F
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Tectum; hearing [motor/sensory]
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Tegementum P/C [4]/F
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Midbrain
RED NUCLEUS SUBSTANTIA NIGRA VENTRAL TEGMENTAL AREA CRUS CEREBRI movement/dopamine |
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Hindbrain: CONTAINS
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Myelencephalon and Metencephalon
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Myelencephalon P/C:
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HINDBRAIN
MEDULLA |
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medulla P/C
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Myelencephalon, fibers of passage
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Metencephalon P/C:
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HINDBRAIN
PONS, CEREBELLUM |
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Pons P/C
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Metencephalon, fibers of passage
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Cerebellum P/F
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Metencephalon
movement / phys. coordination |
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Basal ganglia P/F/C
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Forebrain
regulates motor movement; works w/motor cortex; inhibits and facilitates Striatum / Pallidum |
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Striatum P/C
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Basal Ganglia
Caudate Nucleus & Putamen |
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Pallidum P/C
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Basal Ganlia
Globus Pallidus |
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M pathway ("HOW")
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Retina; Rods, M-Ganglia Cells
LGN layers 1, 2 V1: layer 4Calpha --> 4B (moving edges) V2: thick stripe region (moving edges) V2--> V3, V5 **V3: dynamic form vision **V5/MT: motion-detection input |
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P pathway ("WHAT")
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Retina; Cones, P-Ganglia Cells
LGN layers 3-6 V1: layer 4Cbeta --> 2, 3 **Blob: COLOR **Interblob: ORIENTATION V2: **Thin Stripe receives input from Blob **Interstripe receives input from Interblob V2 --> V3, V4 **V3: mainly from interstripe, dynamic vision **V4: mainly from thin stripe, color |
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Blob
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COLOR
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Interblob
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ORIENTATION
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Akinotopsia (WHAT, CAUSE)
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Strobevision; V5/MT area
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Achromatopsia WHAT/CAUSE
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Total Colorblindness, V4 damage
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Chromatopsia WHAT/CAUSE
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Color vision only, blob cells have more oxygen; more resistant to anoxia [e.g., CO poisoning]
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Object Agnosia
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classically defined as an inability to recognize objects visually in spite of preserved, biological vision
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Balient's syndrome
[and what's a major symptom of it] |
can’t see full visual field at once;
simultanagnosia |
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simultanagnosia
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inability to see two things at once
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Ocular Ataxia
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inability to point accurately
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Ocular Apraxia
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inability to fixate accurately
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Blindsight
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lack of conscious awareness of vision BUT with ability to detect stimuli
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Blob/Interblob WHERE/WHAT
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Layers 2, 3 of Striate Cortex
Blob: COLOR Interblob: ORIENTATION |
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Area V2: Thick/Thin/Interstripe
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Thick: MOTION
Thin: COLOR Inter: FORM IN MOTION |
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V3, V4, V5/MT:
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V3: Dynamic form / moving form vision
V4: Color V5/MT: Motion |
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Cranial Nerve 5:
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Trigeminal; Mastication
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Cranial Nerve 7:
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Facial; face surface muscles
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