CAL 1 Flashcards

1
Q

What does a cell body of a neurone consist of

A

perikaryon and a nucleus.

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2
Q

where in the neurone is the site of protein synthesis

A

the cell body

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3
Q

What does the cell body of the pre-synaptic neurone give rise to

A

the cell body of the pre-synaptic neurone gives rise to dendrites (apical and basal) and an axon

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4
Q

where does the axon arise from

A

the axon hilliock

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5
Q

what is an IPSP

A

this is an inhibitory post synaptic potential

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6
Q

where do inhibitory inputs synapse onto

A

inhibitory inputs commonly synapse onto the cell body (axosomatic synapses) or the axon (axoaxonic synapses).

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7
Q

what does an IPSP do that inhibits the action potential

A

Activation of an inhibitory input generates a graded hyperpolarization this means that the neurone cannot depolarise to reach the threshold point in order to generate an action potential

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8
Q

What is the major role of the apical dendrites

A

receive excitatory input from other nerve cells

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9
Q

what does an EPSP do

A

this is an excitatory post synaptic potential

- it causes depolarisation and generates an excitatory input

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10
Q

what happens at the axon hilliock in order to generate an action potential

A
  • in order to generate an action potential there is summation at the axon hillock which eventually leads to the threshold point being reached
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11
Q

what concentrations of ions are high intracellular then extracullularly

A

intracellularly - potassium, protein negatively charged (anions) are higher

extracellularly - sodium and chloride are higher

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12
Q

The resting nerve cell membrane has a high relative permeability to

A

potassium

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13
Q

what is the typical resting potential

A

-65mv, this approximates to the potassium equilibrium potential

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14
Q

what is the resting potential of a neurone due to

A

potassium leaking out of the non gated potassium channels

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15
Q

what is the equilibirum potential for sodium

A

this is the membrane potential at which there is no net flux of sodium across the membrane
+58mv

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16
Q

what are the two groups that central nervous system neurotransmitters are classified as

A
  • peptide

- non peptide

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17
Q

name some peptide neurotransmitters

A
  • somatostatin
  • substance P
  • Cholecytokinin
  • enkephalins
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18
Q

name some non peptide neurotransmitters

A
  • dopamine
  • glutamate
  • acetylcholine
  • GABA
  • noradrenaline
  • 5-HT
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19
Q

what are the types of non peptide neurotransmitters

A
  • Monoamine
  • amino acid
  • choline esters
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20
Q

name some examples of non peptide neurotransmitters

A
  • Monoamine - dopamine, 5HT, noradrenaline
  • amino acid- glutamate, GABA
  • choline esters - acetylcholine
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21
Q

describe how peptide neurotransmitters are synthesised

A
  • starts with synthesis of peptide neurotransmitters
  • this happens via transcription of the genes in the cell body nucleus, then translation in the cytoplasm
  • this forms the large precursor molecule
  • the precursor molecule undergoes translational maturation and cleavage
  • then transported to the pre-synaptic terminal via fast axonal transport
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22
Q

describe how non peptide neurotransmitters are synthesised

A
  • these are synthesised in the presynaptic terminal from precursor molecules
  • the precursor molecules are taken up by active transport process into the terminal
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23
Q

are there more peptide or non peptide molecule

A

non peptide - these are gene products so are more susceptible to evolutionary change

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24
Q

where are both peptide and non peptide molecules stored

A

they are both stored in vesicles following entry by active transport processes

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25
describe what happens at the presynaptic terminal causing it to release neurotransmitters
- action potential causes the membrane to depolarise - this depolarisation opens calcium channels - this causes calcium ions to diffuse down there concentration gradient - the increase in intracellular calcium ions causes vesicles to fuse with the membrane and release neurotransmitters - the neurotransmitters are released - they diffuse across the synapse and have an effect on the post synaptic cells
26
what is co-transmission
this is when both non-peptide and peptide are released at the same time
27
what is an autoreceptor
- this is a receptor on the pre-synaptic membrane that is the same shape as the neurotransmitter and can either increase or decrease release of the neurotransmitter
28
how is non peptide neurotransmitter terminated
- by active reuptake into the pre-synaptic terminal
29
how are the ways that neurotransmitters can be stopped
- either by reuptake into the pre synaptic terminal | - or degradation by enzymes in the synapse
30
what happens to neurotransmitters that have been reuptaken into the presynaptic terminal
- either degraded or taken back up for storage in the vesicles
31
what are retrograde transmitters
these are lipophillic molecules such as nitric oxide that use an uncovenentianal mechanism of transport - they are not stored in vesicles but they are syntehsised on demand - act as retrograde messengers - released from postsynaptic terminals and act on presynaptic terminals
32
What is the typical synaptic delay (i.e. time between depolarization of the pre-synaptic terminal and the onset of the post-synaptic respons
0.5ms
33
What effect will a decrease in extracellular [Ca⁺⁺] have on synaptic transmission?
inhibit
34
Approximately how many vesicles are there in each terminal?
10,000
35
How rapidly are peptide transmitters transported from the nucleus to the nerve terminal?
400mm/day
36
What effect will blockade of the pre-synaptic autoreceptors have on synaptic transmission?
unpredictable effect | - depends on the type of neurotransmitter
37
Approximately how many molecules of transmitter are stored in each vesicle?
300
38
What effect will an inhibitor of transmitter inactivation have on synaptic transmission?
potentiate (increase)
39
In the central nervous system, approximately how many vesicles fuse with the pre-synaptic nerve terminal in response to the influx of Ca⁺⁺ associated with each action potential?
between 1-10
40
What effect will blockade of the post-synaptic receptors have on the excitability of the post-synaptic neurone?
unpredictable
41
what are the two receptors that neurotransmitters bind to
- ligand gated receptor ion channel | - G protein ion channels
42
what are ligand gated ion channels
1) Ligand gated ion channels are heterooligomeric proteins traversing the membrane,
43
How many subunits do ligand gated ion channels consist of
often consisting of four or five subunits.
44
how short is the time taken for the neurotransmitter to bind to the ligand gated ion channel and for it to open
e time taken for the transmitter molecules to bind and the ion channel to open is short (<<0.1 msec).
45
what does the duration of channel opening in the ligand gated ion channels depend on
The duration of channel opening depends, in part, on the rate of dissociation of the transmitter molecules and the kinetics of channel gating. - Amino acids induce fast neurotransmitter action in the CNS, but most monoamine and peptide neurotransmitters do not activate ligand-gated ion channels, and thus act more slowly, as neuromodulators.
46
what does a G protein channel consist o f
The receptor consists of a single polypeptide chain that traverses the membrane 7 times.
47
describe how a G protein channel works
- single transmitter molecule binds to the G protein and it becomes activated by the displacement of GDP by GTP - this causes the dissociation of alpha GTP, beta and gamma subunits - Usually α GTP, but often β and gamma as well, stimulates the effector to bring about the response, - Return of the G protein to its resting state occurs by α GTP hydrolysing its bound GTP to GDP, with subsequent reassociation with the β and gamma complex
48
The Duration of effects is in msecs applies to...
ligand gated ion channels
49
Single polypeptide chain is the typical structure of a:
G protein coupled receptor
50
Heterooligomeric protein is the typical structure of
ligand gated ion channel
51
This receptor type requires 2 molecules of transmitter for activation
ligand gated ion channel
52
2nd messengers can mediate the effects of
G protein coupled receptor
53
This type of receptor consists of a peptide chain that traverses the membrane 7 times
G protein coupled receptor
54
what does the amplitude of the EPSP depend on
the amplitude of the EPSP depends on the amount of transmitter released, which depends on the number or pre-synaptic fibres activated which, in turn, will depend on the intensity of the stimulus.
55
what happens if the amplitude of the EPSP reaches the threshold
- an action potential will be generated
56
what can membrane depolarisations also result from
I) Influx of Ca⁺⁺ II) Closing of K⁺ channels III) Efflux of Cl⁻
57
What does the action potential result from
(i) an unequal distribution of ions across the membrane due to the activity of the Na⁺/K⁺ pump and (ii) the presence of a population of non gated K⁺ channels which allows K⁺ to leave the cell down its electrochemical gradient (outward K⁺ current). .
58
describe the characterstics of EPSPs
- localised - non propagated potentials result from the transmitter released from the afferent fibres activating a population of ligand gated ion channels
59
what voltage is the depolarisation sufficient enough to open voltage gated sodium channels and trigger an action potential
At about -55mV (threshold), the depolarization is sufficient to open voltage gated Na⁺ channel, hence triggering an action potential.
60
what usually causes inhibition of an action potential
Inhibitory transmitters usually combine with post-synaptic receptors to open channels permeable to Cl⁻ causing a hyperpolarization (Inhibitory Post-synaptic Potential, IPSP). The opening of channels permeable to Cl⁻ and K⁺ usually mediates synaptic inhibition.
61
what does the amplitude of the IPSP depend on
the amplitude of the IPSP depends on the amount of transmitter released which depends on the number of pre-synaptic fibres activated which, in turn, will depend on the intensity of the stimulus.
62
what happens if you have excitation and inhibitory inputs
have an EPSP of reduced potential