Lecture 1 Flashcards

1
Q

What are the 3 steps when it comes to a information transmission in the nervous system?

A

1) sensory input
2) integration to proper motor unit
3) motor output

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2
Q

What are the two main divisions of the nervous system and what are they made of?

A

CNS- brain/spinal

PNS- all nerves that extend from the brain and spinal

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3
Q

Name the two main divisions of the PNS, what kind of information is it?
What sub divisions do these have? What are their functions?

A

1) sensory(afferent): somatic sensory fibers (aware of it, input comes from skin, muscles, joints to the brain) & visceral sensory fibers (unaware of it, from the GI, heart, etc.
2) motor: efferent, transmits impulses from CNS to the effector organs. Broken up into 2 divisions: somatic (in control of) and autonomic (no control)—> fight or flight, etc

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4
Q

Autonomic NS breaks into two divisions, what are they and what is their function?

A

sympathetic–> fight or flight, during activity
parasympathetic–> rest/digest, conserve energy

work opposite to each other

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5
Q

Name the 6 types of Neuroglia

A

astrocyte, microglial cell, ependymal cell, oligodendrocytes, satellite cells, schwann cells

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6
Q

Astrocytes:

What does it look like, general characteristics and main functions.

A

Look like stars
most abundant, highly branched, cling to neurons, synaptic ends and capillaries in the brain.
Support neurons, plays a role in exchange of molecules past the BBB (made of capillaries and astrocytes)

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7
Q

What determines if a molecule will be able to pass the BBB easily or not?

A

size, lipid soluble

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8
Q

Microglial cells:

What it looks like, main function

A

Small, ovoid cells with thorny like branches, migrate to injured neurons and transform into phagocytes to kill pathogens or debris

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9
Q

Ependymal Cells:

Distinctive shape and feature, function

A

columnar or squamous.have cilia, line the cavity and aid in the flow of the cerebral spinal fluid

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10
Q

Oligodendrocytes vs Schwann cells:

Where are they each found

A

oligo: CNS
Shwann: PNS

both wrap neurons with myelin to form the myelin sheath in white matter

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11
Q

Neurons:

1) What is Amitotic?
2) What is the cell body, Rough ER called?
3) What is meant when referring to a Nuclei or Ganglia?

A

1) never divides
2) Soma or perikaryon, Nissle Body
3) Nuclei is a cluster of neural cell bodies in the CNS and Ganglia lie along nerves in the PNS

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12
Q

Dendrites:

Describe what they look like and what their main function is.

A

Short, numerous branches, RECEIVE sensory input and send message to Soma, some have spines

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13
Q

The Axon:

Structure- Where does it arise from? Length? Branched? What is the ending called?

A

arise from the axon hillock, can be short or a meter long (nerve fibers), occasionally branched (axon collaterals), ending is called the axon terminal.

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14
Q

Axon:
Functional Parts- main job? where are signals transmitted from–to? What happens to the signal at the end of the axon? What does it lack? What is anterograde and retrograde?

A

conduct motor output to effector cells.
trasmitted along the axolemma to the axon terminal where the electrical signal is passed chemically via NT at the synapses.
It lacks rough ER and Golgi, gets protein from Stoma.
Anterograde is movement away from the cell, enzymes, Mitochondria, membrane compounds, etc
Retrograde is movement towards the stoma: dead organelle, signal molecules, viruses and bacterial toxins etc.

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15
Q

Multiple Sclerosis:

Describe it, what are some KEY symptoms , what causes it? How can it be spotted under xray? What are treatments?

A

Chronic, relapsing/remitting disorder, causes demyelination of the brain and optic nerve, can be genetic or multifactorial. Causes vision loss, paralysis of eye, vertigo and psychiatric problems. Caused by mutated CD4 (t helper) cells releasing cytokines and attracting phagocytes because it doesn’t recognize myelin as self cells. Can be spotted by finding plaques that are unsymmetrical on each side of the brain. Treated by high dosage of steroid use or interferon.

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16
Q

Progressive Multifocal Leukoencephalopathy (PML):

What does it cause? Where does it affect? What causes it and who is susceptible to it?

A

areas of the brain look whiter. causes limb weakness and speech problems. affects the cortex, caused by the mad cow disease virus and only affects those who are immuno-compromised

17
Q

Guillain-Barre Syndrome

What is the target? How is it diagnosed? How is it treated?

A

PNS targeted, diagnosed by looking at nerve conduction, protein levels. Treated by plasmapheresis (resupply the entire blood stream)

18
Q

Name the 3 types of membrane channels, explain each.

A

ligand gated: substrate must bind to the receptor to open it

voltage: open/close in response to membrane potential
mechanically: open/close in response to physical deformation

19
Q

What is the resting membrane potential? How many Na and K are moved out/in, respectively to maintain polarity by the Na/K atpase? Why is the resting membrane potential negative?

A

-70mv, 3 Na out, 2 K in, it is negative because more Na is pumped out than K pumped in.

20
Q

Define the terms depolarization, repolarization and hyperpolarization.

A

De: Na pumped into the cell, the inside of the cell becomes less negative, membrane potential decreased (towards zero)
Re: K pumped out, cell becomes more negative inside, increased membrane potential (away from zero)
Hyper: more negative than Resting MP
ALL OR NOTHING!

21
Q

What is Absolute Refractory Period? What is Relative Refractory Period?

A

Abs= during de and repolarization, nothing else happens if there is a stimulus, allows for one way transmission and for AP to be an all or none event. Refers to when Na channels open all the way to when they reset

Relative: if the stimuli is really large, it can force a second AP to occur early

22
Q

What 2 factors influence the rate of AP propagation?

What are the 3 nerve fiber classes, describe them.

A

axon diameter , the larger the less resistance, faster
degree of myelination (saltatory conduction)
1) Group A, highly myelinated, large diameter, muscles, skin, etc
2) Group B, lightly myelinated, intermediate diameter
3) Group C, no myelin, smallest diameter

23
Q

What are the 3 different types of synaptic connections/

A

axosomatic–> axon to cell body
axodendritic- axon to dendrite
axoaxonic- axon to axon

24
Q

Explain how information is past across the synapse

A

Fuck her right in the pussy

25
Q

What is Synaptotagmin and what does it do?

A

It binds to Calcium that is flooded in due to the AP and promotes the fusion of synaptic vesicles to neurotransmitters

26
Q

What 3 things occur to neurotransmitters when their function is complete?

A

reuptake by astrocytes
degration by enzymes
diffuse away

27
Q

Explain what inhibitory synapses are in respect permeability of ions.

A

K moves out of cell and Cl moves in, this makes the membrane potential more negative and AP is less likely to occur.

28
Q

What are the two classes of Biogenic amines and give examples

A

catecholamines: dopamine, epinephrine and Norepinephrine
indolamines: serotonin and histamine

29
Q

What are some examples of Peptide and Purine neurotransmitters?

A

peptides: endorphins, substance P
Purines: ATP

30
Q

What is the theorized function of NO for the brain?

A

Formation of new memories

31
Q

What are endocannabinoids? Why are they able to bipass the BBB?

A

THC, weed.

Lipid soluble

32
Q

When referring to Neurotransmitter EFFECTS, what are the two types, explain them with an example

A

Excitatory, increases the chance of an AP, eg: Glutamate

Inhibitory: Decrease chance of AP eg: GABA or Glycine

33
Q

What is DIRECT and INDIRECT action?

A

Direct: binds to own receptor, induced own response
Indirect: uses secondary messangers, such as G proteins, cAMP which can trigger genes or open its own gates or activate enzymes.

34
Q

Two types of receptors for NT, describe each.

A

1) Channel linked (ligand gated), fast and brief response

2) G protein linked (indirect, complex and slow, causes a more widespread reaction)