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 ____

A

Na+
K+

17
Q

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

A

INTO

18
Q

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

A

OUT

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
Q

Neuron-neuron synapses can be _______, but neuron-muscle synapses are ALWAYS _____

A

inhibitory or excitatory
ALWAYS excitatory

26
Q

where are small neurotransmitters assembled?

A

in the terminal

27
Q

where are large neurotransmitters assembled?

A

in cell body but then transported down axon for release

28
Q

what are some examples of large neurotransmitters and what are their functions?

A

Endorphins and Enkephalin (natural painkillers)

29
Q

Inhibiting degradative enzymes → _______ neurotransmitters concentration

A

INCREASES

30
Q

____ = degradative enzyme on presynaptic neuron

A

MAO

31
Q

____ = degradative enzyme on post-synaptic cell

A

COMT

32
Q

What are the 3 ways to deal with Neurotransmitters?

A

Reuptake
Diffuse away into interstitial fluid
Degradation

33
Q

which ways are used to get rid of small vs large neurotransmitters?

A

LARGE: diffusion, degradation
SMALL: reuptake, diffusion, degradation

34
Q

what is IPSP? what can cause this?

A
  • 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
Q

what is EPSP? what can cause this?

A

-input on post-synaptic that increases likelihood of AP firing
-Na+ rushes in → more positive → closer to threshold
- is a graded potential

36
Q

when can a depolarizing IPSP happen?

A

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**