Lecture #23 - The synapse (full pre much but go over last page of paper) Flashcards

1
Q

What’s a synapse?

A

“The junction bw nerve cells, where a nerve impulse is transferred from one neuron to another.”

“Communication bw neurons occurs through a junction called a synapse”

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2
Q

Electrical synapse (city of one cell connected to cyto of other)

  1. Neurons linked by?
  2. Explain gap junctions (three things)
  3. DAP - stands for?
  4. Very fast or slow synapse?
A
  1. Neurons linked by?
    - gap junctions
  2. Explain gap junctions (three things)
    - specific type of membrane channels
    - ‘tunnel’ connecting 2 diff neurons
    - physical link (direct connection)
  3. DAP - stands for?
    - Direct propagate of Action Potential
  4. Very fast or slow synapse?
    - Very fast synapse
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3
Q

Chemical synapse (gap bw cells)

  1. Neurons linked by?
  2. What’s the messenger?
  3. What does the messenger do?
  4. IAP - stands for?
  5. Slow or fast?
A
  1. Neurons linked by?
    - Physical gap between neurons…linked by chemical compound
  2. What’s the messenger?
    - neurotransmitter (released into synaptic cleft)
  3. What does the messenger do?
    - bridges the gap (the synaptic cleft)
  4. IAP - stands for?
    - Indirect propagation of Action Potential
  5. Slow or fast?
    - Slower than electrical synapse

Most synapses in brain are chemical
Heart is connected all by gap junctions so AP just pass through that

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4
Q

What kinda channels in input zone to allow AP to pass down neutron?

A

Stimulus-gated

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5
Q

Depolarisation = trigger or inhibit?
Hyperpolarisation = trigger or inhibit?
(usually)

A
Depolarisation = trigger 
Hyperpolarisation = inhibit
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6
Q

What’re the 8 key components of the chemical synapse?:

A
  1. Presynaptic cell (output zone)
  2. Synaptic knob
  3. Synaptic cleft (the gap)
  4. Postsynaptic cell (input zone)
    - the membrane of post has high density of ion channels
  5. Voltage-gated Ca2+ channels
    - selective to Ca2+
    - in presynaptic cell
    - on the arrival of AP at knob, VGCaC open bc depolarisation of knob…allow extracellular Ca2+ to enter
    - Ca2+ triggers the rapid exocytosis of neurotransmitter molecules from vesicles in knob (trigger fusion of vesicles with pre membrane)
    - relases neurotrans into cleft
  6. Vesicles
  7. Cytoskeleton
    - protein fibres that keep certain structures
    - vesicles interact w/ these for transport
    - vesicles travel to membrane using cytoskeleton
  8. Mitochondria
    - For e.g. Na/K ATPase
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7
Q

Ca2+

  1. What’s the conc in ECF?
  2. Is it high or low inside cell?
  3. Imp for?
  4. Triggers what?
A
  1. 2.2 to 2.6mmol/L
  2. Very low inside (so if chann open, flows inside)
  3. Important for bones and nervous system
  4. Triggers release of vesicles
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8
Q

What does G-protein coupled receptors do?

A
  • Can activate “other K+” channels that aren’t voltage gated

- Don’t allow passage of ions but send messages in cell that can activate

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9
Q

How is the signal transmitted?

A
  1. Neurotrans DIFFUSES across the synaptic cleft to reach the post synaptic membrane
  2. Neurotrans bind to specific receptors aka “stimulus gated channels”
  3. If Na+ chain open - LOCAL depolarisation of the post cell (excitatory signal)
  4. Net depolarisation - called the EPSP (excitatory post synaptic potential)

3’. If K+ [[OR]] Cl- channel open - hyper polarisation (inhibitory signal)

4’. Net hyperpolarisation - called the IPSP )inhibitory post synaptic potential)

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10
Q

The opening of ion channels in the post synaptic membrane may produce a local potential called POSTSYNAPTIC POTENTIAL

Excitatory neurotransmitters cause…..

Inhibitory neurotrans cause……

A

Excitatory neurotransmitters cause both Na+ AND K+ to open. Bc Na+ rushes inward faster than K+ out, there’s temporary depolarisation called EPSP
-If EPSP reaches the -59mV threshold, AP is initiated

Inhibitory neurotrans cause K+ and/or Cl- to open. Cl- rushes in; K+ out. Either event makes the inside of membrane even more -ve than RMP - this temporary hyperpolarisation is called an IPSP
-the post mem less likely to reach the threshold potential; invitation of an act pot is thus inhibited

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11
Q

How is a synapse switched off?

A
  • Excess transmitter released into the cleft
  • Excess transmitter must be removed
    a) Degradation - enzymic (makes compound inactive by break down)
    b) Reuptake - into the bouton (membrane transporter requires ATP so it can be recycled)
    c) Reuptake (diffusion) - into glia cells (reabsorbed)
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