Week 2 - Neuroanatomy Flashcards

1
Q

What is the fundamental difference between somatic nervous system and autonomic nervous system? Explain in terms of afferent and efferent.

A

Somatic Nervous System (SNS)
(interaction with environment)
Afferent nerves (sensory - to CNS)
Efferent nerves (motor - from CNS)

Autonomic Nervous System(ANS)
(Regulates the body’s internal state)
Afferent - from internal organs
Efferent - to internal organs
Sympathetic and parasympathetic nerves (both efferent)

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2
Q

What are the two types of efferent nerves in autonomic nervous system?

A
  1. Sympathetic
    Stimulate (“winds things up”, organise energy in threatening situations)
  2. Parasympathetic (“winds things down”)
    conserves energy

Organs receive inputs from both (push / pull relationship).

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3
Q

What are the clusters of cells in the CNS/PNS?

A

Nuclei for CNS and Ganglia for PNS

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4
Q

What are the clusters of axons in the CNS/PNS?

A

Tracts for CNS and Nerves for PNS

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5
Q

What are “poles”?

A

number of directions for transmission by a neuron

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6
Q

What are the two main types of glial cells in the CNS and PNS? and what is the ratio of glial cells to neurons?

A

Oligodendrocyte for CNS
Schwann cells in PNS

Glial cells outnumber neurones 10:1.

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7
Q

What are the four main types of neurons?

A
  1. Unipolar neuron - sensory neurons transfer information from receptor cells to higher nerve cells
  2. Bipolar Neuron - connecting adjacent cells; typically in sensory system
  3. Multipolar neuron (typical neuron diagram) - transfer information between cells within a single structure; can collect info from many cells
  4. Multipolar neuron - connecting adjacent cells and only has a cell body.
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8
Q

What are the two main types of neurons in the spinal cord (explain in terms of dorsal, ventral, afferent and efferent).

A

Unipolar afferent neurons join the dorsal horn - both somatic (skeletal / sensory) and autonomic (internal organs) systems.

Multipolar efferent neurons have their cell bodies in the ventral root. Their axons project out to somatic and autonomic systems.

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9
Q

What are the three neurophysiological features important for protecting the brain?

A

Skull
Meninges (Dura Mater, Pia Mater, Arachnoid)
Cerebrospinal fluid (CSF)

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10
Q

What is the chemical protection mechanism of the brain?

A

Chemical protection – maintaining chemical balance
The blood-brain barrier
Tightly packed cells along the blood vessel walls of the CNS prevent entry of many (large) molecules.
Good and bad (eg L-Dopa)

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11
Q

From the scalp to the outer layer of the cortex, what is the seven ascending order of protection. From outermost to innermost layer.

A
  1. Scalp
  2. Skull
  3. Dura Mater
  4. Arachnoid meninx or membrane
  5. subarachnoid space (CSF flow
  6. Pia Mater meninx
  7. Cortex
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12
Q

Where is the CSF produced and what happens if drainage of CSF is blocked?

A

Choroid plexus in the fourth ventricle.

If drainage is blocked: hydrocephalus

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13
Q

What is the Myelencephalon? And what is it’s role?

A

Medulla oblongata

Primarily composed of axonal tracts carrying information from the brain to the body and back.

Vital functions- heart rate, breathing

Contains portion of reticular formation (net-like formation) - role in arousal.

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14
Q

What is the Metencephalon?

A

Pons and Cerebellum

Also composed of many tracts of nerves and contains a portion of the reticular formation.

Pons – vital functions relay centre, plays a role in mediating REM sleep.

Cerebellum - sensory and motor control; cognitive; navigation

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15
Q

What is the Mesencephalon and the two main regions?

A

The midbrain:

Tectum
superior colliculus -visual orienting of attention
inferior colliculus -auditory orienting of attention

Tegmentum – portion below tectum
periaqueductal grey matter - autonomic function, motivation, response to threat, descending pain modulation
Substantia Nigra - motor control

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16
Q

What is the famous case of the Frozen Addicts?

A

the discovery of the cause of a local outbreak of sudden, severe parkinsonism in a group of young adults in northern California and how this discovery led to greater insight into Parkinson’s disease.

led a team of investigators to pinpoint the toxicant responsible for the acute loss of dopamine-containing neurons in the substantia nigra, causing the parkinsonism in these patients.

The toxicant was MPTP (pyridine) an unwanted biproduct from a short step synthesis of an illicit synthetic heroin analogue.

17
Q

What are the three main nucleus of the Thalamus?

A

Thalamus (Diencephalon):
1. Lateral Geniculate Nucleus - first synapse after the optic nerve leaves the eye.
2. Medial Geniculate Nucleus - Auditory relay
3. Ventro Posterior Nucleus - Sensorimotor relay.

18
Q

What are the two main cell types of the neo-cortex layers?

A
  1. Pyramidal Cells (large bodies, multipolar, long axon goes down and inward through layers)
  2. Stellate Cells (small, star-shaped short / no axons; transmit info laterally)
19
Q

How does each neo-cortical layers differ in the quantitative aspects of pyramidal and stellate cells.

A

Each layer differs
in the relative concentration of stellate and pyramidal cells
in the relative size and concentration of cell bodies (e.g. layer IV is thick in sensory areas; layer V – mainly pyramidal cells with long axons - in motor areas)

20
Q

How does information pass down the neocortical layers?

A

Vertical flow of information via long axons is the basis of columnar organisation.

21
Q

What is commisurotomies/callosotomies?

A

Antecedent: usually epilepsy
Procedure: callosotomy, anterior commisurotomy
Consequence: reduction of seizures
Behavioural consequence: very little
Experimental consequence: sensory information presented to one hemisphere is not available to guide behaviour in the other hemisphere