exam 2 Flashcards

1
Q

which layer of tissue of the embryo produces the nervous system?

A

ectoderm

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2
Q

six stages of neural development

A

neurogenesis, cell migration, differentiation, synaptogenesis, neuronal cell death, synapse rearrangement

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3
Q

neurogenesis

A

– proliferation of precursors of neurons and glial cells
– marginal zone, intermediate zone, ventricular zone (top, middle, bottom)
– stems cells – undifferentiated cells that can become any type of neuron or glia

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4
Q

neurogenesis in adult brain

A

– possible adult learning and memory
– decline of neurogenesis associated with cognitive decline
– multiple reserves help resist loss of function

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5
Q

brain changes in healthy aging

A

– medial temporal lobe areas involved with memory
– executive pathways connecting basal ganglia and frontal lobes

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6
Q

cell migration

A

radial glia as a “scaffolding”

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7
Q

what regulates migration?

A

cell adhesion molecules, expressed by migrating neuron and radial glia (n-cadherin)

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8
Q

differentiation

A

cells begin to express specific genes

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9
Q

synaptogenesis

A

– synapses form rapidly on dendritic spines of dendrites
– growth of cones regulated by chemical signals (chemoattractants and chemorepellants)
– continues throughout life
– spines proliferate after birth
– cell bodies increase in size

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10
Q

neuronal cell death

A

– apoptosis is the death of cells which occurs as a normal controlled part of development
– access to neurotrophins influences neuronal survival

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11
Q

synapse rearrangement

A

– elimination of extraneous connections and maintenance of functional connections
– also known as synaptic remodeling

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12
Q

Explain the process of neuronal precursor proliferation in the ventricular zone.

A

a small number of precursor cells divide in two; then, in another cycle, each precursor cell divides again, perhaps several more times

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13
Q

What is the role of radial glia in the cell migration stage of neural development?

A

act as a physical scaffold, providing a pathway for newly generated neurons to migrate from the ventricular zone to their final destination in the cortex by extending long, radial fibers that guide the neurons along their journey, essentially acting as “guide rails” for cell migration

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14
Q

Compare & contrast the 2 triggers of cell differentiation that occurs in the 3rd stage of neural development.

A

– Cell autonomous (w/o instructions)
– Driven by genes
– Intrinsic organization seen in vitro
– Induction
– One set of cells determines the fate of nearby cells
– Only occurs in vivo

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15
Q

What regulates the outgrowth of axons & dendrites in the first phase of synaptogenesis?

A

Intrinsic factors (genetics)
Extrinsic factors (environment)

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16
Q

Explain when synaptogenesis starts and when it stops.

A

Synaptogenesis, the process of forming new synapses between neurons, begins shortly after conception during prenatal development and continues throughout life, although it occurs most rapidly during infancy and adolescence, with the peak rate of synapse formation happening in early childhood; it essentially “stops” when the brain reaches maturity and has established its adult number of synapses, which happens gradually throughout the later stages of development and into early adulthood

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17
Q

Describe how death genes regulate apoptosis.

A

– By activating a series of events that leaf to cell death
– In normal cells, there are: caspases
– Are proteases that cut up proteins and DNA
– Are normally inhibited by inhibitors of apoptosis proteins (IAPs)
– Initiating apoptosis
– Starts with a Ca2+ influx
– Ca2+ releases Diablo from mitochondrion
– Diablo binds to inhibitors of apoptosis proteins (IAPs)
– Releases brake on caspases

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18
Q

What are the primary factors that influence apoptosis?

A

– Making adequate number of synapses
– Chemical signals from the targets
– Neurotrophic factors (aka neurotrophins)
– A target derived chemical that acts as if it “feeds” neurons to keep them alive
– Taken up by the axons of innervating neurons
Ex.
– Nerve growth factor (NGF) – regulated sympathetic nervous system growth
– Brain derived neurotrophic factor (BDNF) – involved in guiding synaptic rearrangement

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19
Q

What is the purpose of the 6th stage of neural development, synapse rearrangement?

A

to refine the neural circuitry by selectively strengthening certain synaptic connections while weakening others

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20
Q

Radial Glia:

A

Location: Found in the developing nervous system, particularly in the neural tube.

Role in Cell Migration: Serve as scaffolding for migrating neurons during development. Neurons use radial glia to navigate to their appropriate locations.

Signals for Cell Migration: Key signals include neurotransmitters and guidance cues like netrins and slits, which help guide the migrating cells along the radial glia.

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21
Q

Death Genes and Apoptosis:

A

Regulation of Apoptosis: Death genes encode proteins that activate the apoptotic pathway. They can trigger caspases, which are enzymes that dismantle the cell’s components, leading to programmed cell death.

22
Q

Phototransduction:

A

Process: Light waves are captured by photopigments in the outer segments of photoreceptors (rods and cones).

Mechanism: Light causes a change in the conformation of retinal (a component of the photopigment), leading to the closure of sodium channels, resulting in hyperpolarization of the photoreceptor cell and a decrease in neurotransmitter release.

23
Q

Role of Bipolar, Horizontal, and Ganglion Cells

A

Bipolar Cells: Relay signals from photoreceptors to ganglion cells, contributing to the on-center/off-surround and off-center/on-surround receptive fields.

Horizontal Cells: Integrate and modulate the input from photoreceptors, enhancing contrast and enabling lateral inhibition.

Ganglion Cells: Transmit visual information from the retina to the brain via their axons forming the optic nerve.

24
Q

Visual Pathway:

A

Diagram/Description:
Retina to optic nerve (retinal ganglion cells)

Optic nerve to optic chiasm (where some fibers cross)

Optic chiasm to lateral geniculate nucleus (LGN) of the thalamus

LGN to primary visual cortex (V1) via optic radiations.

25
Q

Olfactory Receptor Cells:

A

Structure: Located in the olfactory epithelium in the nasal cavity.
Axon Projections: Axons project to the olfactory bulb in the brain, synapsing on mitral and tufted cells.

26
Q

Auditory Pathway:

A

Structures:
Cochlea → Auditory nerve → Cochlear nucleus → Superior olivary complex → Inferior colliculus → Medial geniculate nucleus (thalamus) → Auditory cortex.

27
Q

Somatosensory Cortex:

A

Location: Located in the postcentral gyrus of the parietal lobe.

Body Surface Representation: The body surface is mapped in a “homunculus” format, with areas representing body parts proportional to their sensory input.

Effect of Amputation: If a person has their left hand amputated, the corresponding area in the somatosensory cortex may become inactive or re-map to represent adjacent body parts, leading to phantom sensations.

28
Q

Proprioceptive Receptors:

A

Types:
Muscle Spindles: Detect changes in muscle length (stretch).

Golgi Tendon Organs: Detect changes in muscle tension.
Firing Patterns: Muscle spindles fire more during stretching and less during contraction, while Golgi tendon organs fire more during tension.

29
Q

Movement Disorders:

A

Parkinson’s Disease: Characterized by tremors, rigidity, and bradykinesia due to dopaminergic neuron loss in the basal ganglia.

Huntington’s Disease: Results in uncontrolled movements and cognitive decline due to degeneration of the striatum and other areas within the basal ganglia.

30
Q

A contagious virus that specifically targets and destroys spinal alpha motor neurons is called _____.
a. myasthenia gravis
b. Epstein-Barr virus
c. tetanus
d. polio

A

d. polio

31
Q

Why is L-dopa given as a treatment for Parkinson’s disease and not dopamine?
a. Because L-dopa is cheaper.
b. So the patient won’t become addicted to the dopamine.
c. Because L-dopa is able to cross the blood-brain barrier.
d. Because dopamine cannot be made into a pill.

A

. Because L-dopa is able to cross the blood-brain barrier.

32
Q

Adequate Stimulus:

A

type of stimulus that is most effective in eliciting a response from a particular sensory receptor.

33
Q

Doctrine of Specific Nerve Energies:

A

Proposed by Johannes Müller

ex: Stimulation of the optic nerve (e.g., pressure on the eye) results in the perception of light, even though no light is present.

34
Q

labeled lines

A

Different pathways transmit different sensory modalities; for instance, pain is transmitted via specific pain fibers

35
Q

Sensory Adaptation:

A

Tonic Receptors: Respond continuously but slowly adapt to a stimulus.

Phasic Receptors: Respond quickly and adapt rapidly, detecting changes in stimuli.

36
Q

Light Manipulation by the Eye:

A

Cornea: Provides most of the eye’s optical power.

Lens: Fine-tunes focus by changing shape (accommodation).

Iris: Controls the amount of light entering the eye by adjusting the pupil size

37
Q

Cell Types in the Bipolar Layer:

A

Bipolar Cells: Receive inputs from photoreceptors; have ON (activated by light) and OFF (activated by darkness) types.

Horizontal Cells: Provide lateral connections and integrate signals from multiple photoreceptors, modulating the response of bipolar cells.

Amacrine Cells: Facilitate interactions between bipolar and ganglion cells; involved in processing motion and contrast.

38
Q

RODS

A

More sensitive to light, responsible for vision in dim light, do not detect color, high density in peripheral retina

39
Q

cones

A

Responsible for color vision and detail, require more light, concentrated in the fovea (central retina), three types (S, M, L) sensitive to different wavelengths.

39
Q

Two Visual Processing Streams:

A

Dorsal Stream (“Where”): Runs from V1 to the parietal lobe, involved in spatial awareness and motion.

Ventral Stream (“What”): Runs from V1 to the temporal lobe, involved in object recognition and form analysis.

39
Q

Extra-Striate Areas:

A

V2: Processes texture and contour.

V3: Involved in motion and form.

V4: Important for color perception.

MT (V5): Specialized for motion detection.

IT: Involved in object recognition and face perception.

40
Q

Structure of Olfactory Receptor Cells:

A
  • located in the olfactory epithelium in the nasal cavity.
  • have cilia that extend into the mucus layer( odorant molecules bind to receptors)
41
Q

When an odorant molecule binds to its receptor on the cilia

A
  • activates a G-protein coupled receptor pathway
  • an increase in intracellular cAMP
  • opening channels, causing Depolarization
42
Q

First targets of the olfactory bulb

A

piriform cortex, amygdala and entorhinal cortex

43
Q

External Ear Parts and Their Roles:

A

Pinna (Auricle): Collects sound waves and directs them into the ear canal.

Ear Canal (External Auditory Meatus): Channels sound waves to the eardrum.

Tympanic Membrane (Eardrum): Vibrates in response to sound waves, converting them into mechanical energy.

44
Q

Parts of the Middle Ear:

A

Ossicles: Includes the malleus (hammer), incus (anvil), and stapes (stirrup).

Eustachian Tube: Equalizes pressure between the middle ear and the atmosphere.

45
Q

Ossicles

A

ossicles amplify sound vibrations from the tympanic membrane to the oval window of the cochlea.

46
Q

Tensor Tympani and Stapedius muscles

A

stabilize the ossicles and help protect the inner ear from loud sounds by dampening their movement.

47
Q

Auditory Pathway Structures:

A

Cochlea → Auditory Nerve → Cochlear Nucleus (in the brainstem) → Superior Olivary Complex → Inferior Colliculus → Medial Geniculate Nucleus (thalamus) → Auditory Cortex.

48
Q

Causes of Hearing Loss/Deafness:

A

Conductive Hearing Loss: Issues in the outer or middle ear (e.g., earwax blockage).

Sensorineural Hearing Loss: Damage to the inner ear or auditory nerve (e.g., noise exposure).

Central Auditory Processing Disorder: Problems in the brain’s processing of sound.

49
Q
A