neurotransmission Flashcards

1
Q

what structures compose the central nervous system?

A
  • Brain
  • Spinal cord
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what structures make up the peripheral nervous system?

A

sensory neurons - afferent nerves

motor neurons - efferent nerves

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is the difference between the somatosensory system and the autonomic system?

A

somatosensory = neurons that recieve sensory information and control movement of skeletal muscle

autonomic system = neurons that receive sensory information and regulate movement of smooth muscle and cardiac muscle as well as glandular secretion - sympathetic and parasympathetic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what do the terms afferent and effferent mean?

A

afferent = transmit information towards the CNS

efferent = transmit information away from the CNS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what are the two kinds of postsynaptic potentials?

A
  • excitatory post-synaptic potential - small depolarizaiton
  • inhibitory post-synaptic potential -hyperpolarization (holding of resting membrane potential) by opening of K+ channel and the neurotransmitter binding opening Cl- channels
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what is the “threshold voltage”?

A

-55 mV = when a certain spot on the neuron reaches this value, an action potential is generated

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

describe the process of an action potential

A
  • depolarization pushes membrane potential across the action potential threshold
  • reduced voltage opens several voltage-gated Na+ channels in that portion of the plasma membrane - Na+ influx leads to further depolarization
  • voltage gated K+ channels open (and Na+ channels close)- K+ efflux repolarises plasma membrane
  • voltage- gated K+ channels close (leaving plasma membrane hyperpolarized)
  • resting membrane potential restored by Na+/K+ pump
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

describe the ‘action potential graph’ from the perspective of the voltage gated sodium channels/potassium channels

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what is the refractory period?

A

period when a further stimulus applied to a neuron or muscle fiber will not trigger another action potential - membrane is depolarized and the neuron is refractory -

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

can you get smaller / larger aciton potentials?

A

no they are all or none

  • strong stimuli produce action potentials of the same amplitude as weak stimuli - the strength of the stimulus is encoded in the frequency of the action potentials that it generates
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

describe the steps of synaptic transmision

A
  1. action potential reaches and depolarizes axon terminal
  2. depolarisation actiates voltage-gated presynaptic Ca2+ channels (Ntype, Ptype)
  3. localised Ca2+ entry triggers exocytosis of neurotransmitters (NTs) from synaptic vesicles into the synaptic cleft, through the activation of Ca2+ sensitive fusion proteins
  4. NTs diffuse into the synaptic cleft
  5. NTs bind and activate receptors on the post-synaptic membrane
  6. inactivation of neurotransmitters
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

how does an electrical synapse travel between two cells?

A

two cells are connected by gap junctions - formation of channels between the cytosolic compartments of the two cells - permit communication between cells by the direct propagation of ionic current from one cell to the other

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what sort of transmission is between neural cells?

A

chemical transmission - unlike the electrical transmission in muscle cells

the change in voltage cuases the calcium channels to open- this calcium causes the vesicle terminals to bind to the cleft - they release the neurotransmitters

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what types of neurotransmitters are inhibitory?

A

GABA and glycine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what kind of neurotransmitters are excitatory?

A

acetylcholine and glutamate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what neurotransmitters can be both excitatory and inhibitory?

A

serotonin, dopamine, noradrenaline

17
Q

what occurs at an excitatory synapse?

A

the NT at an excitatory synapse depolarises the post-synaptic membrane potential - they continue the depolarization across the post-synaptic cleft so it excites the next channel

18
Q

what occurs at the inhibitory synapse?

A

the NT an inhibitory synpase hyperpolarizes the post-synaptic membrane potential

ex) the binding of GABA A to GABA A receptors on the post-synaptic membrane activates ligand-gated chloride channels - the Cl- influx hyperpolarizes the post-synaptic membrane potential

19
Q

what are ionotropic receptors?

A

they are ligand gated ion channels - NT binding increases permeability to ions

Fast synaptic transmission

20
Q

what are metabotropic receptors?

A
  • G protein couple receptors
  • slower synaptic transmission
  • NT binding triggers activation of G protien that either directly modifies function of ion channels or triggers the production of a chemical second messenger that modifies ion channels
  • mediates short term as well as long term effects (gene expression)
21
Q

local anaesthetics like lidocaine work how?

A

by blocking the voltage gated Na+ channels

22
Q

where are neurotransmitters synthesized?

A

they are synthesized locally within the axon terminal

23
Q

how are neurotransmitters inactivated?

A
  • inactivated/degraded by enzymes in the synaptic cleft or
  • taken up by presynaptic neuron via transporter protein -repackaged and recycled s
24
Q

how do Selective serotonin reuptake inhibitors work?

A

they give serotonin a longer time to sit in the synaptic cleft - allowing more time to be taken up by the receptors

25
Q

myelin is what? what is it made of?

A

it is a fatty sheat around axons formed by

  • schwann cells in PNS
  • Oligodendrocytes in CNS
26
Q

what are the “ nodes of ranvier”?

A

they are the gaps between myelinated regions of the axon - they are dense with voltage gated Na+ channels- action potential appears to “jump’ from node to node

27
Q

what determines nerve conduction velocity?

A

diameter of the axon - larger axons are faster than smaller axons

myelination - myelinated axons conduct faster than unmyelinated axons

28
Q

what is “saltatory conduction”

A

the term for the action potential jumping from one unmyelinated node to the next node

29
Q

What factors interfere with nerve conduction?

A
  • local anaesthetics
  • demyelination
  • cold - cold temperatures slow action potentials
  • ischaemia
30
Q

What is Multiple Sclerosis?

A

autoimmune disease - attack myelin sheat by immune cells (CD4) and antibodies -

symptoms = fatigue, vision problems, tingling and numbness, muscle weakness, impaired balance

-corticosteroids or interferon beta used to reduce inflammation/immune respone

31
Q

what is the compound action potential (CAP) ?

A

CAP is the sum of individual “all or none” action potentials arising more or less simultaneously in a large number of individual axons in a stimulated large “compound nerve”

  • most nerves, axons can vary in diameter, degree of myelination, excitability threshold and conduction spee