Neurons 3 Flashcards

1
Q

What is synaptic transmission?

What are the 2 different ways?

A

The fast process of transferring info BETWEEN neurons or between neurons and muscle fibres

  1. Chemical synapses (mostly occurs this way)
  2. Electrical synapses (through gap junctions)
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2
Q

How does a chemical synapse occur?

A
  1. Depolarisation at the presynaptic terminal causes release of neurotransmitter
  2. Neurotransmitter diffuses across synaptic cleft and binds to receptors in postsynaptic membrane
  3. This initiates opening of a channel and a current in postsynaptic cell
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3
Q

What are the 3 key features of chemical synapses?

A
  1. Specificity: specific neurotransmitters have specific effects on postsynaptic membrane
  2. Complexity: type, time, strength, location, etc.
  3. Plasticity: changes in synaptic structure and function associated with development, learning, aging etc.
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4
Q

What are neurotransmitters? (3)

A
  • Chemical messengers that open/close ion channels
  • Leading to de/hyperpolarisation of POSTsynaptic MEMBRANE
  • Each neurotransmitter can bind to different types of receptors producing different effects on neuron function
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5
Q

What is the postsynaptic membrane?

A

The membrane that receives the signal (binds neurotransmitter) from presynaptic cell

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6
Q

What are excitatory postsynaptic potentials (EPSPs)? (4)

main type of chemical synapses in CNS/PNS

A
  • Evoke DEpolarisation of the postsynaptic membrane
  • Main neurotransmitters: glutamate, acetyl choline
  • Opens channels for Na, K and sometimes Ca
  • Shifts Vm from RMP TOWARDS threshold for AP generation
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7
Q

What are inhibitory postsynaptic potentials (IPSPs)? (4)

main type of chemical synapses in CNS/PNS

A
  • Evoke HYPERpolarisation of the postsynaptic membrane
  • Main neurotransmitters: GABA, glycine
  • Opens K channels
  • Shifts RMP AWAY from threshold
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8
Q

What is direct gating? (2)

A
  • Transmitter binds to receptor/ion channel complex causing pore to open
    (Fast, short lasting)
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9
Q

What is indirect gating? (4)

A
  • Transmitter binds to receptors (eg. GPCR) activating G-protein pathway
  • Leads to production of second messengers (eg. cAMP)
  • Activates protein kinases, phosphorylating ion channel
    (Slower, longer lasting)
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10
Q

What are small molecule (‘classical’) neurotransmitters?

What are the common types? (3)

A

Usually fast, acting directly on postsynaptic receptors.
Common types:
- Amino acids (glutamate, GABA, glycine)
- ACh
- Biogenic amines (dopamine, norepenephrine, serotonin)

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11
Q

What are neuropeptides/neuromodulators?

What are the common types?

A
  • Large molecule chemical messengers - indirect/metabotropic or modulatory action on effects of other neurotransmitters
  • Slow, diffuse action
  • Enkeophalin, substance P, neuropeptide Y
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12
Q

What are the 3 steps in neurotransmitter inactivation/recovery?

A
  1. Diffusion: neurotransmitters removed from synaptic cleft by diffusion
  2. Enzymatic degradation: different enzymes degrade different types of neurotransmitters
  3. Re-uptake/recycling: different forms of transporters remove + move to storage
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13
Q

What is excitotoxicity?

A

The pathological process by which nerve cells are damaged or killed by excessive stimulation by neurotransmitters such as glutamate

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14
Q

What is spatial summation?

A

Excitatory potentials from MANY NEURONS trigger threshold point

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15
Q

What is temporal summation?

A

Many excitatory potentials from ONE NEURON triggers threshold point

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