the developing brain Flashcards

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
Q

what is meant by ‘functional’ in neuroscience methods?

A

temporary changes in brain physiology associated with
cognitive processing (e.g. fMRI)

26
Q

what is the problem of functional neuroscience methods?

A

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
Q

what are functional neuroscience methods that can be used with infants and young children?

A

Electrophysiological response (electromagnetic fields in brain) eg. EEG/ERPS

Haemodynamic response (brain blood supply)
eg. fMRI, fNIRS

28
Q

infant EEG

A

Infant friendly EEG
systems/solutions that allow
quick installation

Infant friendly stimuli

More breaks during the study

29
Q

infant vs adult ERPs

A

Some adult ERP peaks
are present in infants,
but delayed: e.g. visual
ERPs

eg. N1/N290: Perceptual
and/or face specific
component

30
Q

some ERP components only present in infants and toddlers:

A

Negative Central peak

Typically peaks between 300-
700 ms after stimulus onset

Reflect attention

Larger peak reflect higher
attention

31
Q

why is fMRI not ideal for infants?

A

Highly sensitive to
motion artifacts

Loud, restrictive
environment

but some recent attempts
eg. face specific
activity in the brain

32
Q

fNIRS

A

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
Q

how to compute BOLD response?

A

from the difference between emitted and
detected NIR

Hb and deoxyHB absorb of NIR

34
Q

NIRS vs fMRI

A

NIRS can be an appropriate substitute

35
Q

NIRS cons

A

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
Q

NIRS pros

A

Portable

More tolerant of movement