week 9 Flashcards

1
Q

by the time fetus reaches __ weeks, the fetal brain has started productions of all necessary structures/features of brain that exist in adults.

A

8

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2
Q

what are the five EARLY divisions/prenatal phases?

A
  1. induction of neural plate
  2. neural proliferation
  3. migration + aggregation
  4. axon growth + synapse formation
  5. neuron death + synapse rearrangement
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3
Q

what is gastrulation?

A

when embryo transforms from a one-dimensional layer (blastula) and reorganizes into a multilayered + multidimensional structure (gastrula).

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4
Q

what are the 3 layers of cells after gastrulation? what do they form?

A
  1. ectoderm: cells that become surface structure of body (skin, hair, nails, eye lens, sebaceous glands, tooth enamel + brain foundations).
  2. mesoderm: cells that become cardiac muscles, skeletal muscles, smooth muscles/tissue.
  3. endoderm: produces cells that become stomach, colon, liver, pancreas, bladder, etc.
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5
Q

describe nervous system at day 18 post-conception (2)

A
  • ectoderm thickens, leads to dev of neural plate.
  • thickening triggered by chem signals produced by mesoderm.
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6
Q

describe nervous system at day 20 post-conception (2)

A
  • neural groove deepened (develops into CNS).
  • begin to see neural crest (develops into PNS).
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7
Q

what do the lateral, middle, and medial row of the flattened neural groove give rise to?

A

lateral: sensory neurons

middle: interneurons

medial: primary motor neurons

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8
Q

describe nervous system at day 22 post-conception (1)

A
  • crest of neural groove comes together to form neural tube.
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9
Q

at what day post-conception are the major divisions of the brain present?

A

25

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10
Q

approx. how many neurons are produced each minute pre-natal?

A

~250,000

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11
Q

what happens when neurons migrate to the wrong areas of the brain?

A
  • disorders like epilepsy, dyslexia, schizophrenia etc. emerge
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12
Q

what are the 6 stages of nervous system development?

A
  1. neurogenesis
  2. migration
  3. differentiation
  4. synaptogenesis
  5. apoptosis
  6. rearrangement
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13
Q

describe neurogenesis in terms of the neural tube (2)

A
  • neural tube becomes thick/enlarged.
  • innermost layer continues producing neurons while outer parts produce grey and white matter.
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14
Q

describe the 2 processes of migration

A
  • somal translocation: extension develops that leads migration; the cell body follows. local process, takes long time (i.e., 1mm/day).
  • glial-mediated migration: cell moves along a radial glial network (“railroad tracks” that neurons can jump onto). global process, still slow but more effective for long distances.
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15
Q

describe differentiation (3)

A
  • after migration, cells align themselves with others cells and form structures.
  • use Cell-Adhesion Molecules (CAMs) which recognize and adhere to molecules.
  • pass cytoplasm b/w cells.
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16
Q

how can undifferentiated cells be of great promise to treat neurological disorders? provide an example (3)

A
  • could potentially treat neurological disorders by putting undifferentiated cells in affected areas.
  • e.g., sub nigra of ppl with parkison’s.

note: easy to get cell into right place; difficult to ensure it becomes right type of cell.

17
Q

describe roger sperry’s experiment (4)

A
  • wanted to determine if we’re like blank slates or preprogrammed (chemoaffinity hypothesis = axons recognize target cells via chem signals).
  • cut b/w the retina + optic tectum of tadpoles (analogous to their visual cortex).
  • rotated eye 180 degrees and allowed connection to regenerate.
  • frog saw world as upside down, indicating that our synaptic connections are preprogrammed/guided.
18
Q

what are trophic factors?

A

helper molecules that allow a neuron to develop and maintain connections with its neighbors

19
Q

what are the 4 criteria that must be satisfied before concluding that a certain molecule is a trophic factor?

A
  1. cell deficit/death in absence.
  2. cell surplus/survival in presence.
  3. trophic factor produced at target site.
  4. receptors for neurotrophic factors on nerve endings.
20
Q

describe apoptosis (1) and how does this process look like in human embryos (1)?

A
  • normal + necessary cell death.
  • e.g., human embryo begins with 175k at 10 weeks post-conception and loses approx. 20% of all neurons by ~30 weeks as a result of not receiving enough trophic factors.
21
Q

what happened to the mouse lacking ‘death’ gene?

A

brain became so enlarged that it pushed out of skull.

22
Q

describe rearrangement (1), when does this occur for humans (1)?

A
  • synapses rearrange to form optimal connections (mainly dendrite growth).
  • post-natal process for humans.
23
Q

describe synaptic density and arrangement across the lifespan (2)

A
  • looks like “sticks” as newborn, more “branches” form with age, adult looks like a “jungle” [slide 43].
  • over-proliferation of connections followed by period of refinement where most effective connections are maintained and others die.
24
Q

approximately __ percent more synapses than needed are produced.

A

50%

25
Q

overproduction of synapses may underlie the greater ___ of the young brain.

A

plasticity

26
Q

a) which neurons have earliest proliferations and earliest drop-offs?

b) which neurons increase more slowly, reach their peak later and have a longer period of refinement?

A

a) sensory neurons

b) prefrontal cortex

[slide 45]

27
Q

rearrangement of synapses typifies the ___ of that particular development.

A

critical period

28
Q

what happens when there is more activity in one eye than the other, i.e., in cases of infantile cataracts (2)? what does this demonstrate about the role of experience (1)?

A
  • connections from deprived eye to visual cortex shrink, while connections from the good eye expand.
  • if not treated before critical period, restoring vision in cataract eye will not produce normal sight because brain is not using info from that eye.
  • demonstrates that experience affects how brain organizes itself.
29
Q

what does the prefrontal cortex play a role in? (3)

A
  • working memory
  • planning and carrying out sequences of actions
  • inhibiting inappropriate responses
30
Q

T or F: with age, reorganization levels in the brain decrease.

A

true

31
Q

what is the denate gyrus part of? what is its significance?

A
  • denate gyrus = part of hippocampus
  • evidence of neurogenesis in the dentate gyrus in the adult brain.
32
Q

T or F: despite the hippocampus shrinking with age, it produces enough new cells to mitigate effects of aging?

A

false