the developing brain Flashcards

(36 cards)

1
Q

history: middle ground perspective

A

interaction between environment and genetic factors

eg. Piaget/neuroconstructivism

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2
Q

what are the different theories within the nature/nurture debate?

A

blueprint analogy

predetermined development

probabilistic development

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3
Q

describe Gottlieb’s different views of development

A

Predetermined development

Probabilistic development

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4
Q

what is Predetermined development?

A

genes–> brain structure–>brain function–>experience

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5
Q

what is Probabilistic development?

A

genes<–>brain structure<–>brain function<–>experience

effects of genes on brain structure themselves are probabilistic: specify approx. how and where neurons develop

variation, not copy = MZ twins

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6
Q

what are the steps within prenatal brain development?

A

cell division

cell specialisation

neural tube formation

neural tube differentiation

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7
Q

neural tube formation

A

proliferative zones: neurons and glial cells produced

250,000 neurons produced/min

neurons migrate to final location

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8
Q

what occurs during neural tube formation?

A

develops into spinal cord and brain

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9
Q

what structural features emerge from constraints?

A
  • folded cortex emerges from having lots of neurons
  • pattern of gyri/sulci pulled into shape by tension of axon bundles
  • Hebbian learning: Spontaneous electrical activity enables networks to form eg. retina
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10
Q

what causes the postnatal increase in brain size?

A

synaptogenesis

myelination

glial cell proliferation

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11
Q

what is plasticity?

A

experience
dependent change in neural
functioning

can lead to small but observable structural changes

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12
Q

how is plasticity evident in the brain?

A

increased grey matter: new synapses, dendrites, axon collaterals, glia cells

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13
Q

what is functional brain development?

A

prenatal brain
damage can lead to major reorganisation of
tracts

eg. AH with no right hemisphere

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14
Q

how is functional brain plasticity limited?

A

Spontaneous electrical activity enables networks to form
intrauterine – connections not fully lost

Opportunities for major reorganisation are time-limited =critical or sensitive periods

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15
Q

what is filial imprinting?

A

the process
by which young animals learn
to recognise the parent
- 15hrs-3 days
- movement is crucial

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16
Q

what are the 2 main features of critical and sensitive periods?

A
  1. Learning takes place within a limited window
    o But opportunity can be extended in lack of experience
  2. This learning is hard to reverse by later experiences (but can generalise to similar objects) (preference can be changed after)
17
Q

phenomic discrimination between ‘r’ and ‘l’ is an example of…

A

critical and sensitive periods

18
Q

what are the explanations of c+s periods?

A

genetically programmes synaptogenesis followed by reduced plasticity

closure of window initiated by learning

19
Q

what is the empiricist view on innate knowledge?

A

newborn mind is a blank state

20
Q

what is the nativist view on innate knowledge?

A

we are born with some knowledge

21
Q

what is the more modern view on innate knowledge?

A

Innate = readiness to learn

Knowledge or behaviour that arises in the absence of appropriate
experience

eg. cat visual cortex
eg. preferences

22
Q

prenatal ultrasound shows:

A

structure: different types of tissue have different physical properties

creates STATIC maps

23
Q

How can we
investigate
brain
development?

A

prenatal ultrasound

prenatal MRI

behavioural methods

24
Q

from behaviour, we can infer:

A

brain development

eg. Preferential looking paradigm

25
what is meant by 'functional' in neuroscience methods?
temporary changes in brain physiology associated with cognitive processing (e.g. fMRI)
26
what is the problem of functional neuroscience methods?
Usually, we ask participants to perform some kind of task or to sit/lay still and look at images Infants won’t perform tasks and they won’t even stay still
27
what are functional neuroscience methods that can be used with infants and young children?
Electrophysiological response (electromagnetic fields in brain) eg. EEG/ERPS Haemodynamic response (brain blood supply) eg. fMRI, fNIRS
28
infant EEG
Infant friendly EEG systems/solutions that allow quick installation Infant friendly stimuli More breaks during the study
29
infant vs adult ERPs
Some adult ERP peaks are present in infants, but delayed: e.g. visual ERPs eg. N1/N290: Perceptual and/or face specific component
30
some ERP components only present in infants and toddlers:
Negative Central peak Typically peaks between 300- 700 ms after stimulus onset Reflect attention Larger peak reflect higher attention
31
why is fMRI not ideal for infants?
Highly sensitive to motion artifacts Loud, restrictive environment but some recent attempts eg. face specific activity in the brain
32
fNIRS
measures BOLD signal (blood oxygen-leveldependent contrast) using near infrared spectrum Skin, tissue, and bone are mostly transparent to NIR light Measures the concentration changes of oxyHb and deoxyHb focally, related to brain activity
33
how to compute BOLD response?
from the difference between emitted and detected NIR Hb and deoxyHB absorb of NIR
34
NIRS vs fMRI
NIRS can be an appropriate substitute
35
NIRS cons
fNIRS has lower spatial resolution Only the surface of the cortex can be imaged Often only a few sensors are used above a certain brain area
36
NIRS pros
Portable More tolerant of movement