Synapses Flashcards

1
Q

what are the 3 different kinds of synapses?

A

-Axon + cell body (Axosomatic)
-Axon + dendrite (axodendritic)
-Axon + axon (axo-axonic)

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2
Q

What happens in depolarization?

A
  1. The action potential triggers voltage gated Na+ channels to open
  2. Na+ rushes in, inside of axon becomes less negative and reaches threshold
  3. voltage gated Ca+ channels open, Ca+ moves in (down its concentration gradient)
  4. Ca+ triggers synaptic vesicles with neurotransmitters in it to fuse with membrane and release neurotransmitter into synaptic cleft
  5. below threshold Ca+ channels close, Ca+ pumps will now pump Ca+ out (using energy)
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3
Q

where are voltage gated Na+ channels? voltage gated Ca+ channels?

A

Voltage gated Na+ channels traverse whole axon, but Ca+ channels are only on the tip

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4
Q

_________ are channels where ligand binds to protein, it opens and lets an ion through

A

Ionotropic channel (ligand- gated channel)

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5
Q

Ionotropic channels are _____, while metabotropic channels are _____

A

fast, slow

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6
Q

______ are channels where ligand binds and there is a signaling cascade in the cell

A

Metabotropic channel (usually GPCR)

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7
Q

can ligands have both metabotropic or ionotropic effect ?

A

YES: GABA-a: binds to ionotropic, but GABA-B binds to metabotropic

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8
Q

____________ is the enzyme that catalyzes the creation of Ach

A

Choline acetylase/Choline acetyltransferase

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9
Q

________ is the enzyme that breaks down Ach

A

Acetylcholinesterase (ACE)

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10
Q

where are the degradative enzymes usually located?

A

post-synaptic cell

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11
Q

what is end-plate potential?

A

when Ach binds to ligand gated channels on muscle fiber → channels open → Na rushes in → graded potential (graded potential in muscle fiber)

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12
Q

contrast neuron-muscle junction and neuron-neuron junction

A
  • Neuron-Muscle junction:
    Large area for neurotransmitters
    LARGE depolarization
    ~60mV change
    Graded potential

-Neuron-Neuron junction:
has small area
depolarization is small
only 1mV change

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13
Q

Ach channel is a ________ cation channel

A

monovalent

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14
Q

what determines the direction of monovalent cations through the Ach channel?

A

Concentration gradient
Charge difference

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15
Q

More Na+ ______ neuron, More K+ _____ neuron bc Na+/K+ pump

A

outside, inside

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16
Q

At rest _____ driving force is much greater than ____

17
Q

(-) DF for (+) ion = going ____ cell

18
Q

(+) DF for (+) ion = going ____ of cell

19
Q

________ has ligand gated channels that bind Ach and allow Na+ to enter

A

End plate region

20
Q

what are the steps at end plate regions?

A

Ach binds to Ach ligand gated channel → Na+ goes in at end plate region → Na+ diffuses and causes depolarization within the muscle fiber → if you reach threshold outside end plate, voltage gated Na+ channels open → AP fires → muscle fiber contracts

21
Q

Normal threshold = _____ depolarization from rest, but graded potentials are usually _____mV

A

~15mV
~60mV

22
Q

why is graded potential so much higher than threshold?

A

it Exceeds threshold dramatically to ensure that the muscle fires

23
Q

________ blocks degradation of AcH

A

Eserine
- causes Ach concentration to increase

24
Q

_______ blocks Ach ligand gated channels

A

Curare
- will never reach threshold since ACH cant trigger channels

25
Neuron-neuron synapses can be _______, but neuron-muscle synapses are ALWAYS _____
inhibitory or excitatory ALWAYS excitatory
26
where are small neurotransmitters assembled?
in the terminal
27
where are large neurotransmitters assembled?
in cell body but then transported down axon for release
28
what are some examples of large neurotransmitters and what are their functions?
Endorphins and Enkephalin (natural painkillers)
29
Inhibiting degradative enzymes → _______ neurotransmitters concentration
INCREASES
30
____ = degradative enzyme on presynaptic neuron
MAO
31
____ = degradative enzyme on post-synaptic cell
COMT
32
What are the 3 ways to deal with Neurotransmitters?
Reuptake Diffuse away into interstitial fluid Degradation
33
which ways are used to get rid of small vs large neurotransmitters?
LARGE: diffusion, degradation SMALL: reuptake, diffusion, degradation
34
what is IPSP? what can cause this?
- input on post-synaptic neuron that reduces likelihood of AP firing -K+ rushes out → more negative → farther from threshold -Cl- channel opens → Cl- rushes in → more negative → farther from threshold
35
what is EPSP? what can cause this?
-input on post-synaptic that increases likelihood of AP firing -Na+ rushes in → more positive → closer to threshold - is a graded potential
36
when can a depolarizing IPSP happen?
just depends on the driving forces and equilibrium potentials; driving force can switch EX: Cl- below Equilibrium potential causes depolarization, but once it hits Eq. potential it causes mV to decrease ** look on summary, its confusing**