4 Synaptic Transmission Flashcards

1
Q

What is a synapse?

A

Synapses are junctional zones between neurons
- they are unidirectional - signals go one way
- there is an inevitable delay - time taken for the released neurotransmitter to diffuse across the synaptic cleft (around 20nm)
from presynaptic side diffusing to the postsynaptic side

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2
Q

Describe synaptic transmission

A
  • It is the transmission of info from neuron to target (e.g. motor neuron to skeletal muscle via NMJ)
  • Synapses transform info from electrical to chemical signal (from AP to neurotransmitter)
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3
Q

Name the different types of axons:

A
  • Axo-dendritic – axon to dendron
  • Axo-axonic – axon to axon
  • Axo-somatic – axon to the cell body (soma)
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4
Q

What are neurotransmitters?

A

They are endogenous chemicals (made by the body) that enable neurotransmission

Different types:

  • Peptides
  • Amino acids: e.g. Glutamate, GABA
  • Catecholamines: e.g. Noradrenaline
  • Other: serotonin, acetylcholine (NMJ)
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5
Q

Describe the presynaptic events during synaptic neurotransmission

A
  1. Action potential comes down the axon
  2. It reaches voltage-gated Ca2+ channels, which open
  3. This lets Ca2+ move into the cell, down its concentration gradient (high [Ca2+] outside cell, created by Ca2+ pump)
  4. This causes vesicles to bind to the pre-synaptic membrane
  5. And releases neurotransmitter molecules across the synaptic cleft by exocytosis - which diffuses and binds to receptors on the postsynaptic membrane
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6
Q

Describe Ionotropic receptor (direct)

A

A receptor is a protein (with a binding site)
- specific, sensitive, saturated
It is a ligand-gated ion channel

The neurotransmitter (ligand) binds to and opens ion channels in the postsynaptic membrane
- this changes the ionic permeability of the postsynaptic cell membrane and hence the Vm of the postsynaptic cell

This is very rapid (1ms)

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7
Q

Describe the depolarisation/excitatory events that follow, after Neurotransmitter release

A
  1. Once neurotransmitter binds to receptors on the postsynaptic membrane, it opens the ion channel
  2. This lets in Na+ ions, which causes the postsynaptic membrane to depolarise
  3. This causes an action potential to be produced in the postsynaptic cell
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8
Q

Describe Metabotropic channels (indirect)

A

In indirect gating, the channel is inward-looking, responding only to chemical messages from inside the cell
- Link with the outside world is provided by a second protein that straddles the membrane + responds to transmitters/stimuli on the outside by triggering off a chemical response on the other side of the membrane, resulting in the required message being sent to the channel

This intracellular communication may involve one intermediate or a cascade of several of them
- very often the first link in the chain is formed by a G-protein Guanosine triphosphate (GTP)-binding protein

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9
Q

Describe Excitatory postsynaptic potentials and Inhibitory postsynaptic potentials

A

If the neuron is excitatory, transmitter binding to the postsynaptic membrane causes transient depolarisation as:

  • Excitatory postsynaptic potential (EPSP)
  • (+ve ions enter, or -ve ions leave postsynaptic membrane)

Inhibitory neurons release neurotransmitters that cause transient hyperpolarisations:
- Inhibitory postsynaptic potentials (IPSPs)

EPSP and IPSP amplitudes are graded with incoming signals(s) strength;

  • so if there is more neurotransmitter
  • more depolarisation
  • threshold potential is reached
  • action potential is produced
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10
Q

Describe how temporal summation is achieved using EPSP

A

Post-synaptic events for EPSP:

  • more stimuli/neurotransmitter
  • this creates a larger depolarisation
  • known as temporal summation
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11
Q

Describe filtering, with respect to synaptic transmission, and postsynaptic potentials

A

Most of the information received by neurons at dendrites represents sensory ‘noise’

  • Postsynaptic potentials (PSPs) are passive responses that degrade rapidly as they travel toward the cell body
  • degradation is enhanced by the dendrite’s inherent electrical leakiness + lack of myelin
  • So a small PSP may never reach the cell body

PSPs generated by a strong presynaptic activity will activate VG-ion channels across the length of the dendrite
- these enhance the signals + increase their likelihood of reaching the cell body

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12
Q

Describe the integration of synaptic signal transmission

A

Signals may integrate at the dendritic level

- PSPs may combine with PSPs arriving from other synapses as they travel toward the soma - known as Summation

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13
Q

Name the 2 types of summation

A

2 types:

  • Spatial
  • Temporal
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14
Q

Describe temporal summation

A

Occurs because the potential produced by a brief synaptic current fall relatively slowly
- possible to get a summation of the effects of repeated stimulation if the frequency of firing of the afferent fibre is high enough

BUT

  • many EPSPs are needed for one AP to be produced out at the axon hillock
  • many in for one out
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15
Q

Describe the events that occur in inhibitory ionotropic receptors (hyperpolarisation)

A
  • An inhibitory neurotransmitter (Like GABA)
  • opens Cl- ligand-gated Cl-channels
  • allowing Cl- ions to enter
  • hyperpolarising the postsynaptic membrane
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16
Q

Describe inhibitory synapses

A

Interneurons are needed, as most neurons can only excite the next neuron
- So, when an interneuron is fired, it inhibits the next motor neuron

  • E.g. when the leg is extended, the quadriceps muscle is extended, and its motor neuron is excited, but the motor neuron for the hamstring excites an interneuron, which inhibits the hamstring.
17
Q

Describe inhibitory Postsynaptic potential - IPSP

what neurotransmitter is involved, and the receptors involved

A

The transmitter is most likely glycine or GABA

  • GABA (y-Aminobutyric acid)
  • the most common inhibitory neurotransmitter

Receptors:

  • GABA-a - ionotropic
  • GABA-b - metabotropic

Functions:
- muscle tone, pain modulation, anxiety, and brain development

18
Q

Describe how inhibitory synapses function:

A

GABA binds to receptors:

  • and opens ligand-gated Cl- channels
  • which move in down their concentration gradient
  • and make the post-synaptic cell membrane more negative - hyperpolarisation
  • this makes producing an action potential harder

This same principle also applies to K+ ions, but they move out of the cell

19
Q

Describe the postsynaptic electrical events during inhibitory postsynaptic potential

A

Inverse of EPSP

  • doubling up of inhibitory input (summation), doubles the signal
  • more negative inflexion of Vm - more hyperpolarisation
  • Inhibition occurs, instead of triggering depolarisation
  • If inhibition happens after excitation, depolarisation is not prevented, it is merely delayed
20
Q

Describe the MOA of diazepam

A

Diazepam - used to control anxiety and seizures

MOA:

  • Drug binds to a specific benzodiazepine binding site on the GABA receptor
  • Causing Cl- channel to favour the open state
  • thus, the neuron is reduced inactivity due to not being able to trigger an AP