Brain Development Flashcards

(85 cards)

1
Q

Describe the development of the nervous system from early embryonic stages through adulthood.

A

The nervous system develops in an intricately coordinated process from early embryonic stages all the way through childhood, adolescence, and adulthood. During early development, the brain forms the ability to dynamically transfer information across billions of interconnected neurons. This enables the coordination and control of mental and bodily functions, including perception, cognition, and movement.

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2
Q

Embryonic stage

A

The embryo is initially formed through fertilization, which occurs when a sperm cell and an egg cell unite into a single cell. This fertilized egg cell, or zygote, starts dividing through the process of mitosis to generate the cells that make up an entire organism.

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3
Q

The three layers

A

Sixteen days after fertilization, embryonic cells form three layers that develop into different body tissues.
* endoderm
* mesoderm
* ectoderm

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4
Q

Endoderm

A

The endoderm, or inner tissue, is responsible for generating the lining tissues of various spaces within the body, such as the mucosae of the digestive and respiratory systems.

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5
Q

Mesoderm

A

The mesoderm, or middle tissue, gives rise to most of the muscle and connective tissues.

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6
Q

Ectoderm

A

The ectoderm, or outer tissue, develops into the body’s outer layer of skin, hair, nails, as well as the nervous system. It is probably easy to see that the outer tissue of the embryo becomes the outer covering of the body.

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7
Q

When does the human nervous system begin to form?

A

Two weeks into embryonic development, the human nervous system begins to form. As the embryo develops, a portion of the ectoderm differentiates into the precursor for the tissue of the nervous system.

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8
Q

What is the neural plate and how does it contribute to nervous system development?

A

Cells that differentiate from the ectoderm form a neural plate, which folds inward to create a neural groove lined by neural folds. These folds fuse to form the neural tube, setting the foundation for the brain and spinal cord.

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9
Q

What is the neural crest and how does it contribute to the development of the nervous system?

A

Cells from the neural folds eventually separate from the ectoderm to form a cluster of cells referred to as the neural crest, which runs lateral to the neural tube. Neural crest cells migrate away and develop into several parts of the peripheral nervous system (PNS), including the enteric nervous system that governs the function of the gastrointestinal tract.

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10
Q

Where does the CNS develop?

A

The Central Nervous System develops along the neural groove.

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11
Q

What happens during the third week of embryonic development?

A

During the third week, the anterior end of the neural tube develops into the brain, and the posterior portion forms the spinal cord. This basic arrangement leads to more complex nervous system structures by the fourth week.

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12
Q

What are the three primary vesicles of the developing brain?

A
  • the forebrain (prosencephalon)
  • the midbrain (mesencephalon)
  • the hindbrain (rhombencephalon)
  • they are generated by the anterior end of the neural tube which begins developing into the brain
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13
Q

Where is each primary vesicle located in the neural tube?

A

Forebrain is uppermost, midbrain is next, and hindbrain is lowest.

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14
Q

When do the primary vesicles differentiate into secondary vesicles?

A

Primary vesicles begin to differentiate into five secondary ones by the 5th week of embryonic development.

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15
Q

Secondary vesicles

A
  • telencephalon
  • diencephalon
  • mesencephalon (midbrain)
  • metencephalon
  • myelencephalon
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16
Q

How does the forebrain (prosencephalon) differentiate?

A

It divides into the
* telencephalon -> becomes cerebrum: cerebral cortex, hippocampus, basal ganglia
* diencephalon -> thalamus + hypothalamus

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17
Q

Thalamus and hypothalamus roles

A

Thalamus= the central relay hub for sensory signals Hypothalamus = involved in homeostasis and regulating functions including hunger, sleep, and mood

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18
Q

What happens with the midbrain?

A

It remains as the mesencephalon, composed of the tectum, cerebral aqueduct, tegmentum, and cerebral peduncles. It is involved in head/eye movements, motivation, and reward.

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19
Q

How does the hindbrain (rhombencephalon) differentiate?

A

It divides into the metencephalon (forms pons and cerebellum) and myelencephalon (forms medulla oblongata - breathing, digestion, heart rate, blood pressure).
* cerebellum = 10% of brain’s mass; coordinates movement, posture, and cognition
* The cerebellum connects to the rest of the brain via the pons, because the pons and cerebellum develop out of the same vesicle.

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20
Q

Brain stem

A

Is composed of the structures formed by the midbrain and the hindbrain, with the exception of the cerrebellum -> midbrain, pons, medula oblongata

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21
Q

What are the two main types of cells in the brain?

A

Neurons and glial cells (neuroglia).

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22
Q

What are neurons, and what is their primary function?

A

Neurons are electrically excitable cells that transmit signals (action potentials) to other neurons. They are the fundamental units of the brain and nervous system and are responsible for communication, sensation, movement, and information processing.

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23
Q

What are glial cells, and what is their main role?

A

Glial cells, or neuroglia, are support cells that help neurons function and communicate. They do not transmit electrical signals but provide essential support for the nervous system

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24
Q

How many main types of glial cells are there, and where are they found?

A

There are six main types of glial cells: four in the central nervous system (CNS) and two in the peripheral nervous system (PNS).

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25
CNS Glial Cells
* Astrocyte - support * Oligodendrocyte - insulation, myelination * Microglia - maintenance of neural networks * Ependymal cell - creating cerebrospinal fluid
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PNS
* Satellite cell - support * Schwann cell - insulation, myelination
27
What is the first stage of neuron growth after the neural tube closes?
The first stage of neuron growth begins after the neural tube has closed. This is called neural proliferation, and begins in the ventricular zone of the neural tube.
28
When does neurogenesis (new neuron generation) begin in embryonic development?
Neurogenesis begins about four weeks after conception. Neurogenesis = the process of generating new neurons
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When does most neurogenesis in the human telencephalon occur?
Most neurons in the telencephalon (cortex, hippocampus, basal ganglia) are generated before birth. After birth, neurogenesis extensively occurs in the cerrebellum. * the bulk of neurogenesis (i.e., the 86 billion neurons) in the CNS occurs between the fourth week post-conception to 18 months after birth—during this early developmental period, approximately 4.6 million neurons are generated every hour
30
What are the cells formed during neural proliferation?
Neural stem cells are formed during neural proliferation.
31
What are the two basic types of stem cells, and how do they differ?
Pluripotent cells can become any cell type in the body, while multipotent cells can form the embryo and extraembryonic tissues (though often "multipotent" is compared as being more limited than pluripotent)
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What is the significance of pluripotent stem cells in medicine?
Pluripotent stem cells are being studied for regenerative treatments (e.g., diabetes, spinal cord injuries, heart disease) because they can develop into any cell type.
33
What do neural stem cells produce during CNS development?
Neural stem cells are special cells which produce radial glial cells, which then differentiate into neurons and glial cells
34
What is the ultimate result of neural proliferation?
Neural proliferation generates billions of cells that develop into the complex structure of the central nervous system (CNS).
35
What can newly formed neurons do after they are generated?
They may stay and continue dividing or migrate to other parts of the nervous system.
36
What is neuronal migration?
It is the process by which neurons move from their original location to a new target location in the nervous system.
37
Where does migration occur for central nervous system (CNS) neurons?
Migration remains within the neural tube for CNS neurons.
38
Where does migration occur for peripheral nervous system (PNS) neurons?
Migration for PNS neurons may occur across different neural regions.
39
What are immature neurons like during migration?
They lack fundamental neuronal characteristics such as axons and dendrites.
40
What supports neuronal migration?
Sophisticated molecular and cellular signaling that pulls and pushes immature neurons to their targets.
41
Describe the general pattern of neuronal migration.
Migration typically follows an inside-out pattern: neurons travel from the inside of the neural tube outward to their target.
42
What are the two main modes of neuronal migration?
Radial migration = Neurons are guided by radial glial cells to move toward the brain surface, establishing the layered structure of the neocortex (primary mode). Tangential migration = Neurons move orthogonally to the direction of radial migration, sometimes to the surface of the CNS. * these are not mutually exclusive, neurons may alternate between these modes during their migration.
43
What are the two main mechanisms of neuronal migration?
Somal translocation = An extension from the neuron’s soma leads it to its target, used in both radial and tangential migration. Glial-mediated migration=Immature neurons "climb" along extended glial cells to reach their target locations; specific to radial migration.
44
What happens after neurons reach their target locations?
They develop dendrites and axons, enabling communication and the formation of functional neural circuits.
45
What is aggregation in the context of neuronal development?
Aggregation is the process by which migrating neurons align and integrate with other neurons to form neural circuits.
46
What are the two key mechanisms that support neuronal aggregation?
Cell-adhesion molecules on cell surfaces recognize and bind to molecules on other cells, enabling cell-to-cell interactions and tissue stabilization. Gap junctions form communication channels between adjacent cells, allowing exchange of ions and metabolites like glucose.
47
What do cell-adhesion molecules do?
They recognize and bind to molecules on other cells, enabling cell-to-cell interactions and helping to stabilize tissue.
48
What are gap junctions, and what is their function in neuronal aggregation?
Gap junctions are communication channels between adjacent cells that allow the exchange of ions and metabolites such as glucose, promoting biochemical coupling.
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What is the result of neuronal aggregation and integration?
These processes facilitate neuronal interactions and integration, ultimately forming the neural circuitry of the human nervous system.
50
What is neuronal cell death, and why is it important during development?
Neuronal cell death is the elimination of neurons in the nervous system. It occurs extensively during development and actually supports healthy brain development by refining neural networks.
51
What are the two main types of neuronal cell death?
Apoptosis (programmed, controlled cell death) and necrosis (passive, accidental cell death).
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What is apoptosis?
Apoptosis is active, programmed cell death that selectively eliminates excess and immature neurons, supporting proper neuronal connectivity and network maturation.
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What is necrosis?
Necrosis is passive, accidental cell death resulting from trauma, toxins, or oxygen depletion. It is characterized by cell swelling, membrane rupture, and leakage of cellular contents. It can result from a stroke, where disrupted blood flow leads to accidental cell death, or TBI. Excessive necrosis is associated with pathologies such as Alzheimer's Disease and Parkinson's disease.
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How do apoptosis and necrosis differ in their effects on surrounding tissue?
Apoptosis efficiently dismantles and removes dead neurons, minimizing disruption. Necrosis leaves behind cellular debris, which can disrupt surrounding brain tissue.
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Why is understanding and regulating cell death important?
Understanding and regulating cell death is crucial for preserving brain function and preventing neurological diseases.
56
What was the traditional view about new neuron generation in the adult human brain?
Until about 25 years ago, it was believed that new neurons could not be generated after birth, although it remains a controversial topic.
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Where is adult neurogenesis most consistently observed in the brain?
* Subventricular zone of the lateral ventricles * Subgranular zone in the dentate gyrus of the hippocampus * Such neurons often do not survive or integrate into existing neural circuits.
58
What is neuroplasticity?
Neuroplasticity is the brain’s ability to reorganize or “rewire” its connections in response to experience.
59
How does learning relate to brain structure?
Learning something new physically changes the structure of your brain through neuroplasticity.
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How does the brain store information?
The brain stores information in networks of modified synapses, and activating these networks allows retrieval of the information
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What is Hebb’s rule?
“Neurons that fire together, wire together.” If two neurons are active at the same time, the synapses between them are strengthened.
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What is long-term potentiation (LTP)?
LTP is a persistent strengthening of a synaptic connection based on simultaneous activation of neurons.
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What role do NMDA receptors play in LTP?
NMDA receptors, normally blocked by magnesium, open when rapid presynaptic inputs depolarize the postsynaptic neuron, allowing calcium to enter and trigger AMPA receptor insertion.
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What happens to AMPA receptors during LTP?
AMPA receptors migrate from inside the postsynaptic cell to the membrane, making the neuron more responsive to glutamate and strengthening the synapse.
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What is long-term depression (LTD)?
LTD is the weakening of synaptic connections, often by removing AMPA receptors from the membrane, making the neuron less
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Why is LTD important for learning and memory?
LTD weakens and prunes unused synapses, allowing important connections to stand out and making learning more efficient.
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How do drugs of abuse relate to LTP?
Some drugs of abuse co-opt the LTP pathway, leading to synaptic strengthening that can contribute to addiction.
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Is neuroplasticity only about strengthening synapses?
No, neuroplasticity also involves weakening some synapses (via LTD) to refine neural circuits.
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Is synaptic strengthening specific?
Yes, LTP is specific to neurons activated simultaneously, strengthening only those connections.
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Sensitive periods
Sensitive periods refer to developmental time windows during which experiences have an especially strong impact on brain organization. While similar experiences can still affect the brain outside of these sensitive periods, the consequences for brain reorganization will not be as strong. Involves heightened neuroplasticity
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Critical periods
Critical periods refer to the limited time windows during which experiences, or lack thereof, have lasting effects on brain function and behavior. Disruptions during critical periods due to atypical experiences or adversity may lead to irreversible changes to brain structure. Involves heightened neuroplasticity.
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How do sensitive and critical periods differ?
Sensitive periods offer broad windows for experience to shape neural circuitry, while critical periods are a subset that can result in irreversible changes to the brain.
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Example sensitive period
Language acquisition (especially second language learning) is a sensitive period—peak proficiency is more likely when exposure occurs in early childhood. A study found that childrenm(Chinese+ Korean) who began learning the second language (English) before age 7 were able to reach proficiency akin to native English speakers; children arriving between age 7 and puberty were less proficient; and after puberty, an individual’s second language proficiency is likely to remain low. These findings support a brain-maturation account, such that the ability to learn languages gradually declines and ultimately flattens as the brain matures. This is not to say learning a second language is impossible after puberty, it just becomes harder, because Lower neuroplasticity after the sensitive period contributes to slower and less successful second language learning.
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Example critical period
Can be exemplified in sensory development and first-language learning. Depriving an animal of visual input during infancy leads to irreversible vision impairment because the brain reorganizes to prioritize input from the non-deprived eye.
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What is cross-modal plasticity?
Cross-modal plasticity is the brain’s ability to reorganize so that regions normally used for one sense (e.g., vision) process input from other senses (e.g., touch or hearing) after sensory l
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How does cross-modal plasticity affect individuals with early blindness?
Their occipital cortex (usually for vision) shifts to process tactile and auditory sensations, and this reorganization can persist even if vision is restored.
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Language as a critical period
In the early 1970s, the tragic story of Genie, an adolescent girl who for most of her childhood experienced severe isolation and neglect, caught the world by storm. When discovered, Genie was unable to communicate verbally with language. Researchers studied Genie’s linguistic development over many years and concluded that, despite initial progress in speech and grammar, her language proficiency remained severely impaired
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What is adolescence considered in terms of brain development?
Adolescence (ages 10–24) is widely considered a sensitive period for brain development due to significant social, cognitive, and emotional changes.
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Adolescent Brain
Substantial neuroimaging research has shown that the frontal lobes, which include regions of the brain involved in executive function, such as the prefrontal cortex, are late-developing and undergo significant maturation that continues well into adolescence. Subcortical regions, on the other hand, develop much earlier, around early adolescence. Parallel to these brain development findings, prior work indicates that adolescence is marked by increased sensation-seeking and risk-taking behaviors
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Can risk-taking in adolescence be positive?
Yes, some risk-taking is essential for identity formation, decision-making skill development, and fostering independence.
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Neural efficientcy and neuroplasticity
high neuroplasticity and flexibility in a brain network corresponds to low stability and efficiency, and vice versa.
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How is brain development influenced by external factors prenatally
Prenatal brain development is highly sensitive to external (environmental) factors, especially because the brain is forming its basic structure and circuitry during this time. * maternal nutrition * maternal stress * substance exposure -> alcohol, nicotine, drugs * infections and viruses * hormonal imbalances * ocygen supply * medication use * social factors (DV, poverty)
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How is brain development influenced by external factors postnatally
* nutrition * appropriate stimulation * secure caregiver attachment * environment (clean/dirty) * exposure to stress/trauma * sleep quality * screen time and social media use * illness
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What brain regions are responsible for drive and priority and how do they vary between adolescents and adulthood?
Prefrontal Cortex (PFC) * Function: Planning, decision-making, prioritization, impulse control. * Subregions: *Dorsolateral PFC: Goal-setting, working memory, abstract reasoning. Ventromedial PFC: Valuation and emotional decision-making. Orbitofrontal cortex: Evaluating rewards and consequences. 📌 Develops Last: The PFC is not fully mature until the mid-20s, making adolescents more prone to impulsivity and short-term thinking.