Wk11 Neuroplasticity & Brain Damage Flashcards

1
Q

what are two windows ‘periods’ which show time dependence? What do they mean?

A

Critical period - asbolutely essential the experience occurs 
Sensive period - experience in this can still have an influence outside interval

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2
Q

What can experience/use of neural circuits achieve? 4

A

Maintenance 
Neurogenesis
Synapse formation
Myellination

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3
Q

What does “use it or lose it” imply about nature vs nurture?

A

Nurture is a key part of how things are established and maintained, both are important.

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4
Q

what are the effects of environmentally deprived mice? 2 (neuronal + behavioural)

A

Fewer synapses and dendritic spines 
Poor depth and pattern perception

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5
Q

what illustrates the effect of critical periods in deprived/open eye mice?

A

long term deprivation is not drastically worse than short term. One week alone causes a lot of damage, little more is acquired after that

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6
Q

When adult rats are exposed to enriched environments where was neurogenesis found? 2

A

Dentate gyrus of HC + olfactory bulbs

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7
Q

What is associated with adult rat neurogenesis in enriched environments? 2

A

Exercise and interaction with environment — not enough to just sit around in the new environment

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8
Q

What evidence shows that exercise is superior to learning alone, for neurogenesis? When do these benefits emerge?

A

Van Praag et al 2000: rats in Runner and Enriched conditions had new cell survival than Learning alone. After one day learning shows new cells, but these only sustain in exercise conditions.

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9
Q

What did voss et al 2013 show about adult neurogenesis in enriched, running, run+enriched?

A

Running was a key to increasing dentate gyrus new cells

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10
Q

how does the object sniffing test for rats work? What does it tell us?

A

Rats are measured on how long they sniff three objects. 24 hrs later a new object is introduced and the sniffing time for this is assessed relative to old objects. This measures rats preferentially exploring novel objects.

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11
Q

What do object sniffing tests show about adult neurogenesis in rats?

A

Rats sniff novel objects more when exercise or enrichment are provided, but the more noticeably when Ex and En are provided together.

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12
Q

What was a problem with early experiments on rat adult neurogenesis? How is this controlled these days?

A

Exercise and enrichment were confounded. Housing is used to separate the two influences.

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13
Q

Does exercise induced adult neurogenesis happen in humans and where? What tasks are involved in testing this?

A

Yes, shown in dentate gyrus.
Auditory list learning.

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14
Q

What happens to kittens with a shut eye from birth to 2.5mo? What does this illustrate?

A

no contralateral activation of ocular dominance columns. Critical period for the development of these cells.

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15
Q

What happens to kittens with an eye shut from 12 mo to 38 mo? What does this show?

A

Overall V1 cortical activity diminished but no change in ocular dominance. Sensitive period where deprivation can still have negative effects.

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16
Q

What are the phases of activity-dependent myelination?

A
  1. ATP is released and taken by OPC to form oligodendrocytes 
2. Action potentials signal astrocytes to myelinate
3. Neuronal firing modulates adhesion molecules
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17
Q

Does social isolation cause reduced myelination? What the implications?

A

Yes. But in rats. this may be a potential mechanism for a range of psychosocial mental problems, but its a large leap to apply this to humans.

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18
Q

What demonstrates neuroplasticity of sensory cortex maps?

A

When vision is displaced through prism lenses, auditory maps compensate and shift. Within a couple of days.

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19
Q

Can cortical digit representation increase in adults? How long does this effect last?

A

Yes, increased for trained movements, but specific to that movement. Lasted up to 8 weeks without training.

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20
Q

What is anterograde degeneration?

A

From the point of damage, further connections die

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21
Q

What is retrograde degeneration?

A

Backwards from the point of damage, the cell dies

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22
Q

What is trans neural degeneration?

A

Damage affects a whole network of neurones, damage spreads.

23
Q

What are the cumulative effects of concussions? 2

A

Internal bleeds
linear and rotational forces lead to cell death (microtubules)

24
Q

What type of damage do we see and not see in concussions?

A

Not structural neuronal damage, but cell death due to microtubules damage.

25
Q

What do P300 EEG responses show about footballers and concussions?

A

People with concussions show less responsivity to unattended stimulus

26
Q

Is a blow to the head necessary for a dead injury?

A

No, even pressure waves from a nearby explosion can increase intracranial pressure and brain motion.

27
Q

What are two types of closed hear injruies?

A

Contusions (bruise from brain slamming skull) 
Haematomas (bleeds, sheared blood vessels)

28
Q

What is Oedema?

A

brain swelling due to fluid

29
Q

What are two ways closed head injuries can cause loss of consciousness?

A

Downward pressure on brainstem 
Brain moving forward twists inside skull, disrupting brain stem functions

30
Q

How do brain injuries cause epilepsy??

A

Disrupted tissue starts to impair neural activity

31
Q

What are things that can happen in a penetrating head injury? 5

A

Closed HI: 
- oedema 
- loss of consciousness
- epilepsy 
- infections
- scarring (epilepsy)

32
Q

How does TBI cause behavioural disturbances?

A

Neurones that resprout atonal projections form unwanted connections.

33
Q

How much oxygen does the brain take up?

A

20% of O2 consumption

34
Q

What is a haemorrhage?

A

Bleed into the brain

35
Q

What is ischaemia? What are 3 types?

A

Disruption in blood supply; thrombus, embolus, arteriosclerosis

36
Q

How long before ischaemia develops consequences?

A

Typically a few days to see consequences

37
Q

What is an infarct?

A

Area of dead tissue caused by stroke

38
Q

What is a penumbra?

A

Area surrounding dead tissue (infarct) which is alive but dysfunctional

39
Q

Can penumbras be recovered? How?

A

Yes there is a potential for recovery. They can be supplied blood from other vessels and function rehabilitated.

40
Q

Why do doctors not usually right away how bad stroke damage will be?

A

The penumbra has not yet died, its functions may be retained.

41
Q

What is secondary energy failure in stroke? How is it caused?

A

Cerebral hypoxia leads to mitochondrial failure. Even when blood supply restored after stroke, neurones can still die.

42
Q

What is peculiar about the inflammatory effect of microglia? And what could this mean?

A

Microglia can act from a distance and so interfere with other areas of the brain which were not damaged. (People present as having TBI consistent and inconsistent symptoms. This is why)

43
Q

What are key variables influencing neural regeneration in adults? 2

A
  1. Capacity is high in early development and drops with maturity 
2. PNS and CNS work differently (PNS better due to Schwann cells)
44
Q

How does neural regeneration work in the PNS if Schwann cells not damaged?

A

Axons can re-grow through myellin sheaths.

45
Q

What happens in the PNS if there is complete but small separation of axons and myellin?

A

Axons may regrow but into the wrong sheaths, signals get mixed.

46
Q

In the PNS, what happens if there is large separations of nerves due to damage?

A

Axons may regrow into a tangle with no destination, antero- and retro-grade degeneration.

47
Q

What happens in the PNS when an axon degenerates?

A

Collateral sprouting. Neighbouring neurons can begin to synapse on the target/vacated sites.

48
Q

What is a new line of therapy for PNS axon all regeneration?

A

Growth hormone.

49
Q

Why doesn’t collateral sprouting happen in undamaged areas?

A

Active neuronal connections inhibit each other and create boundaries.

50
Q

What are 2 mechanisms of CNS reorganisation?

A
  1. New connections via collateral sprouting 
2. Strengthen existing connections (due to less neighbouring inhibition)
51
Q

When can age be good and bad for recovery of function? And why? 2

A

During neurogeneis = good 
- brain just makes more neurons

During neural migration = bad 
- neurones are still connecting to endpoints

52
Q

Can damage after neural migration phases be recovered from?

A

Yes, after migration there is a period of synaptogenesis which can allow compensatory synaptogenesis.

53
Q

How can rehabilitative training post stroke be improved?

A

Restraining competing limbs. because neural systems are competing, more energy can be given to affected areas.