neuronal transmission Flashcards

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1
Q

define the structure of a neurone.

A

dendrites - recipient of information from other neurones
soma - involved in controlling processing in the cell and integrates information
axon - carries information from the soma to the terminal boutons
terminal boutons - communication point with other neurone

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2
Q

what is the function of the neural membrane?

A
  • separates the extracellular env from the intracellular env
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3
Q

what do protein structures do?

A

detect substances outside the cell, allow access of certain substances into the cell.

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4
Q

what figure indicates the RMP?

A

-65 to -75mV (inside the cell, more negatively charged).

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5
Q

what causes there to be a membrane potential?

A

the movement of particles across a membrane due to diffusion and and electrostatic pressure.

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6
Q

define diffusion.

A
  • molecules move from an area of high concentration to an area of low concentration.
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7
Q

salt spilts into which particles?

A

Na+ and Cl-

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8
Q

describe how the equilibrium potential is reached?

A
  • P+ ions move across membrane by diffusion force, as P+ ions move there is an increase in electrical potential across the membrane (more +ve on one side, more -ve on the other).
  • eventually a point is reached when the diffusion force = electrostatic force (EP)
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9
Q

which particles are mostly located outside the neurone? and which ones are mostly inside?

A

sodium (Na+) are mostly outside and want to get in, whereas potassium (K+) is mostly inside so wants to get out.

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10
Q

describe the RMP steps.

A
  1. high conc of Na+ outside neurone, high conc of K+ inside neurone
  2. at rest, more K+ channels open than Na+ channels.
  3. Na+ move into neurone and K+ out due to diffusion.
  4. as more K+ than Na+ can diffuse, the membrane comes to rest near the K+ EP.
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11
Q

what is the equation for the EP

A

Eion = 61 x log (ion)o / (ion)ii

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12
Q

define the sodium-potassium pump.

A

maintains the ionic cone gradients across the membrane and therefore RMP.

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13
Q

define ATP.

A

ATPA is broken down to release energy which forces ions to move against their conc gradients, pump uses energy to move sodium to restore balance between Na+ and K.

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14
Q

define key aspects to the action potential.

A
  • nerve impulse
  • allows communication within the neurone, along the axon
  • generated at the axon hillock
  • generated either by summation of converging inputs from the dendrites or by electrical stimulation.
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15
Q

what happens during conductance?

A
  • following a small stimulation theres a small degree of depolarisation that decays along the length of a neurone, known as decremental conductance.
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16
Q

describe voltage-gated channels.

A
  • open when the membrane becomes depolarised
  • different degrees of depolarisation open the channels
  • look at properties using voltage clamp experiments
  • postive membrane potentials result in inactivation of Na+ channels.
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17
Q

how are voltage clamp experiments carried out?

A
  • inject a current into the axon to create a steady membrane potential
  • record the membrane current: product of what ions are moving across the membrane.
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18
Q

state the types of membrane currents.

A
transient inward current followed by a slow outward potential.
sodium current (fast) - movement of ions into the neurone through Na+ channels. 
potassium current (slow) - movement of the ions out of the neurone through K+ channels.
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19
Q

outline the 8 steps to the AP.

A
  1. at RMP, majority of channels are closed
  2. small depolarisation opens a few Na+ channels, Na+ begins to move into the neurone, leading to depolarisation.
  3. if stimulation is large enough (threshold) the majority of Na+ channels open and Na+ moves into cell.
  4. as neurone continues to depolarise, some K+ channels are opened, allowing K+ to leave the neurone.
  5. at postive potenitals Na+ become deactivated. remaining K+ channels open, K+ continues to leave (inside now positive)
  6. membrane potential decreases and becomes negative (repolarisation).
  7. K+ channels begin to close and Na+ channels return t their closed normal state. The MP drops below the RMP (hyperpolarisation).
  8. final K+ channels close, MP returns to the RMP.
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20
Q

outline the steps to AP in as few words as possible.

A
  1. rest: Na+ and K+ closed
  2. Na+ channels open, na+ enters.
  3. some k+ channels open, k+ leaves.
  4. Na+ channels become refractory, no more na+ enters, remaining k+ channels open.
  5. k+ continues to leave, membrane returns to RMP.
  6. k+ channels begin to close, na+ channels rest.
  7. remaining k+ close, k+ inside the neurone diffuses away.
21
Q

true or false: propagation of the AP along the axon is unmyelinated (unidirectional).

A

true - only goes one way.

22
Q

define the myelin sheath.

A

fatty tube placed around the axon by either an oligodendrocyte or a Schwann cell.

  • oligodendrocyte - asymmetrical, forms myelin around axons in brain and spinal cord.
  • Schwann cell - asymmetrical, wraps around peripheral nerves to form myelin sheath.
23
Q

what occurs during a myelinated AP?

A

AP can only occur at the nodes of a ranvier as this is where k+ and na+ can pass through channels.

24
Q

where is depolarisation built up?

A

at the nodes of the ranvier, and the decays through myelinated sections.

25
Q

what is the advantage to myelinated axons?

A
  • less APs are needed to send a nerve impulse along a myelinated neurone, its much more efficient.
26
Q

what does damage to the myelin sheath lead to?

A

multiple selerosis.

27
Q

what toxins can block channels?

A

tetrodotoxin can block na+ channels.

a-dendrotoxin can block k+ channels.

28
Q

what is the different between electrical and chemical synapses?

A

electrical synapses are rare in mammalian neurones, whereas chemical synapses are common, the junction between the neurones is very small in electrical synapses and used to communicate between neurones, but the gap and much bigger in chemical ones where neurotransmitters are released from the presynaptic neurone to communicate with the post-synaptic neurones.

29
Q

where can the synapse be located?

A
  • oxodendritic
  • axosomatic
  • axoaxonic
30
Q

define the EPSP.

A

activation of an excitatory synapse leads to local and small depolarisation of the postsynaptic cell, EPSP decays over the length of the dendrite.

31
Q

the closer the synapse is to the soma, the greater …

A

its influence on the production of an AP in the axon.

32
Q

where are all inputs summated?

A

at the soma.

33
Q

describe the process of synapses.

A
  1. AP travels down axon
  2. when it gets to synapse, depolarisation opens voltage-dependant calcium channels
  3. influx of calcium leads to neurotransmitter release
  4. neurotransmitter binds and activates receptors on the dendrites of the post-synaptic cell
  5. leads to depolarisation or hyperpolarisation of post-synaptic cells
  6. spreads to soma where summation occurs
  7. if enough depolarisation, AP is generated at axon hillock.
34
Q

state the criteria for neurotransmitters.

A
  • chemical synthesised presynaptically
  • electrical stimulation leads to the release of the chemical
  • chemical produces physiological effect
  • terminate activity
35
Q

describe dale’s law.

A
  • if a particular neurotransmitter is released by one of a neurones synaptic endings, the same chemical is released at all synaptic ending of the neurone.
36
Q

outline the steps of neurotransmitter action.

A
  1. NT molecules are synthesised from precursors under influence of enzymes
  2. NT molecules are stored in vesicles
  3. NT molecules that leak from their vesicles are destroyed by enzymes
  4. APs cause vesicles to fuse with the presynaptic membrane and release their neurotransmitter molecules into the synapse.
  5. bind with autoreceptors and inhibit subsequent NT release.
  6. bind to postsynaptic receptors
  7. deactivated either by re-uptake or enzymatic degradation.
37
Q

what happens during release of the neurotransmitter?

A
  1. synaptic vesicle containing NT ‘docked’ at synaptic membrane
  2. depolarisation of pre-synaptic neurone leads to opening of calcium channels and calcium influx
  3. vesicles fuse with the synaptic membrane and releases NT into the synapse
  4. vesicles detaches from the docking zone.
38
Q

describe post-synpatic action of the neurotransmitter.

A
  • NT binds to receptors on post-synaptic membrane, which affects the activity of the post-synaptic cell, the configuration of the receptors make them specific for different NTs.
    e. g opening of an ionic channel = ionic receptor
    e. g. activates an internal 2nd messenger = metabotropic cell.
39
Q

what is the ionic receptor?

A
  • protein subunits around a central pore (allows ions to go in and out)
  • fast transmission - ions movement leads to an immediate change in the post-synaptic cell.
40
Q

describe the difference between excitatory and inhibitory fast transmission.

A

in both transmissions ion channels open, in the excitatory transmission there is movement of positive ions into the neurone, depolarisation and EPSPs, whereas in inhibitory transmission there is movement of negative ion into the neurone, hyperpolarisation and IPSPs.

41
Q

what is the metabotropic receptor?

A

G-protein coupled receptors activation…

  1. NT binds to receptor and activates g-protein
  2. g-protien spilts and activates other enzymes
  3. breakdown of GTP turns off g-protein activity
  4. series of chemical reactions that lead to an amplification of the single-second messenger system.
42
Q

give examples of major classes of neurotransmitters.

A

amino acids, monoamines, soluble gases, neuropeptide, acteylcholine.

43
Q

define glutamate.

A

fast excitatory NT in CNS, very widespread, activates different types of receptors: mGlur, NMDA, AMPA, Kainate
- involved in learning and memory

44
Q

define GABA.

A
  • major inhibitory NT, activates an iontropic receptor when opens a chloride channel, leading to hyperpolarisation.
  • involved in anxiety.
45
Q

name drugs that enhance GABA function =.

A
  • ethanol
  • benzos
  • barbiturate
  • neurosteroids
46
Q

what can EPSP be decreased or abolished by?

A

IPSPs from inhibitory neurones that are active at the sametime.

47
Q

what can EPSPs be enhanced by?

A

excitatory neurones that are active at the sametime.

48
Q

state aspects to autoreceptors.

A
  • located on pre-syn terminal
  • respond to NT in syn cleft
  • generally g-protein coupled
  • regulate internal process controlling the synthesis and release of NT.