BRAIN DEVELOPMENT FROM INFANCY TO ADOLESCENCE Flashcards

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1
Q

Nervous system

A

The nervous system is not a static network of interconnected elements; rather, it is a plastic (changeable), living organ that grows and changes continuously in response to its genetic programs and its interactions with the environment

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2
Q

Cells in the human nervous system

A
  • Neurons are the basic functional units of the nervous system. They take in information from other neurons (reception), integrate those signals (conduction), and pass signals to other neurons (transmission)
  • Glial cells nourish, protect, and physically support neurons and are thought to be particularly critical in brain development. One type of glial cell, the oligodendrocyte, covers the axons of neurons with myelin, a substance critical to the effective functioning of the brain
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3
Q

Speed of propagation of the action potential

A
  • Speed of propagation of the action potential is determined by:
    o Diameter of axon (bigger=faster)
    o Presence or absence of a myelin sheath
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4
Q

Myelination

A

The myelin can block the potassium and sodium channels
Because the myelin is prohibiting the ion transfer, that ion transfer only happens in the gaps. How does that speed up the action potential?
Like a Mexican wave – individuals sitting down and standing up down propel it, it’s because each person waving triggers the next person along. That’s what’s happening in an axon

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5
Q

Embryonic Development of the Nervous System

A
  • At 18 days post conception, an embryo consists of 3 layers of cells: endoderm, mesoderm, and ectoderm
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6
Q

The ectoderm of the embryo thickens to form the neural plate

A

o The cells in the ectoderm become specialised tissue that will borm the brain and spinal cord
o This sheet of specialised cells is called the neural plate

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7
Q

Cross section of the developing neural tube

A
  • The neural tube will grow to form the central nervous system
  • The neural crests will develop into the peripheral nervous system
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8
Q

Cross Section of the developing neural tube

A

This developing neural tube begins to form discrete enlargements of vesicles. These embryonic vesicles will develop into the major regions of the brain: the forebrain, midbrain and hindbrain.

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9
Q

Development of the Nervous system: Neurogenesis

A
  • Neurogenesis – the mitotic division of nonneuronal cells to produce neuroblasts
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10
Q

Development of the Nervous system: Cell Migration

A
  • Cell migration – the massive movements of nerve cells or their precursors to establish distinctive nerve cell populations (nuclei in the CNS, layers of the cerebral cortex etc)
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11
Q

Development of the Nervous system: Differentiation

A
  • Differentiation – of cells into distinctive types of neurons or glia
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12
Q

Development of the Nervous system: Synaptogenesis

A
  • Synaptogenesis – the establishment of synaptic connections as axons and dendrites grow
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13
Q

Development of the Nervous system: Neuronal Cell Death

A
  • Neuronal cell death – the selective death of many nerve cells
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14
Q

Development of the Nervous system: Synapse Rearrangement

A
  • Synapse rearrangement – the loss of some synapses and development of others to refine synaptic connections
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15
Q

Neurogenesis

A
  • The production of nerve cells is call neurogenesis
  • The cells that will give rise to neurons begin as a single layer along the inner surface of the neural tube. These cells divide in a process called mitosis and gradually form a closely packed layer of cells
  • Immature neurons produced via mitosis are called neuroblasts
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16
Q

Cell migration

A
  • Cells migrate to establish distinct nerve cell populations (nuclei in the CNS, layers of the cerebral cortext etc)
  • Cells are still immature (no axons, dendrites)
  • Cells migrate outwards, so innermost cell layer is the oldest
17
Q

Differentiation

A
  • Once immature neurons have completed their migration and have reached the embryonic region where they become functional units of the nervous system, differentiation takes place
  • Differentiation allows the cell to acquire the distinctive appearance of neurons characteristic of that particular region (i.e – cells become distinct types of neurons or glia as processes are formed)
  • Two influences on differentiation
    o Intrinsic self-organisation
    • Cell-autonomous differentiation
    • Cell uses information contained within itself (e.g. the cell transcribes a particular subset of genes to make the particular protein it needs)
    o Neural environment
    • Induction-based differentiation
    • Cell uses information from neighbouring cells
18
Q

Synaptogenesis

A
  • Establishment of synaptic connections
    o Growth of axons, dendrites and synapses
  • Tips of axons and dendrites have growth cones
    o Filopodia (fine outgrowths) and Lamellipodia (sheetlike outgrowths) adhere to extracellular environment
    • Growth cone is pulled along, extending the axon or dendrite in that direction
  • Growth pathway is guided by chemicals released from the target cell
    o Chemoattractants and chemorepellents act on specific growth cones
  • Connections are affected by experience
19
Q

Neuronal Cell Death

A
  • As strange as it may seem, neuronal cell death is a crucial phase of brain development, especially during prenatal stages
  • The physiological process of eliminating differentiating neurons is very important for the correct design of regions and circuitry in the nervous system
  • Selective death on many nerve cells
    o Naturally cocuring cell death (apoptosis)
    o Sculpting and refining process
  • Between 20-80% of cells in a given region will die
20
Q

Many neurons die during normal early development (part 2)

A
  • The basic principle of selective cell death is that neurons must establish synaptic contacts with other neurons (or neuromuscular plates with muscles) in order to survive: those immature neurons that do not establish functional connections are eliminated
  • Cells compete not just for synaptic sites, but for a chemical that the target structure makes and releases. Such target-derived chemicals are called neurotrophic factors
21
Q

Synapse Rearrangement

A
  • Finally, the process of synapse rearrangement allows the synaptic connections between the remaining cells to be reorganised
    o Active synapses are maintained, inactive synapses are retracted, and new synapses are also formed
22
Q

Development of the brain: Key influences: Intrinsic Factors

A

o Genes

23
Q

Development of the brain: Key influences: Extrinsic Factors

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o Nutrients
o Drugs and toxins
o Cell-cell interactions

24
Q

Development of the brain: Key influences: Neural Activity

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• Post-natal sensory input (experience)

25
Q

Structural Brain Changes: Cortical Changes

A

o Infancy and early childhood is characterised by a dramatic period of synaptogenesis, followed by an adaptive process of cell death and pruning. There is another notable surge of synapse growth just before puberty.
o The strengthening or elimination of synapses is dependent on environmental demands or experience; those that are more often used are strengthened and those that are rarely used are eliminated
- Overall, grey matter (neuronal cell bodies, dendrites, and glial cells) development follows an inverted U pattern of growth, first thickening in volume, peaking, and then thinning

26
Q

White matter changes (myelinated axons)

A
  • White matter increases in a roughly linear pattern throughout childhood, adolescence, and into early adulthood
  • However, different brain structures myelinate at different times: myelogenetic cycles
    o Sensorymotor pathways myelinate early
    o Regions mediating higher order functions myelinate late (e.g. the prefrontal cortex)
27
Q

Development of the Prefrontal Cortex

A
  • Synaptic density – reaches adult levels in adolescence
  • Myelination – thought to be complete in the early 20s
  • Therefore, there is relatively ‘late’ maturation of the prefrontal cortex
    o What are the implications of this?
    • To answer this, we ned to know what the PFC does!
28
Q

Functions of the prefrontal cortex

A
  • ‘executive’ functions
  • working memory
  • planning and organisation
  • inhibitory control
  • self-monitoring
  • insight and judgement
  • cognitive flexibility
  • selective and sustained attention