for exam Flashcards

1
Q

what is axonal transport?

A

transport of proteins through microtunules in acons
fast approx 1000mm/day
cna ba anterograde and reterograde

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2
Q

what is the acon hillock

A

the part of the axon which first emerges from the soma

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3
Q

what is the axon proper

A

the main body of the axonwhat are the acon terminalsthe very end o the acon where boutons are formed this is what synapses start from

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4
Q

what are the acon collaterals

A

banches o the axon so just before the terminals

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5
Q

what ae the five features through which neurons can be classified and what are the options?

A

shape: stellate or yramidal(cal also be spiny
axons: golgi 1-long golgi2-lcal
number of neutrites: unipolar bipolar or multipolar
connections: primar sensory-connected to sensory surfaces eg skin and retina motor-conneted to muscle interneurons-connected to other neurons

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6
Q

which cells produce myelin in the cns

A

oligodendrocytes

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7
Q

which cells produce myelin in the pariforal nervous system

A

schwan cells

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8
Q

describe the shape and structure of an strocute

A

star shaped and contains few organelles and microglies

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9
Q

what is the functio of astrocytes

A

povide mechanicl and metabollic support whilst reguating the flow of ions in extracellular fluid and being inbolved in repair
they are most numerous in brain

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10
Q

what is the structure of olligodendrocytes?

A

numerous organeles and microtubules as they make myelin and are involved in repair processes in th cns

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11
Q

what does the spinothalamic pahwa signal?

A

pain

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12
Q

a higher diameter of the axon mens ther i Ales or B more resitance

A

less

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13
Q

where are neuropeptides synthesised?

A

vell body

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14
Q

what percentage of all synapses do chemical synapses mae up?

A

95%

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15
Q

how long is the synaptic delay ?

A

0.5ms

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16
Q

which neurotransmitter does currarie compete with and at which receptor?ps its a reversible antagonit…

A

acetlchlllline t the nicotinic receptor

17
Q

what are the efects of curarie?

A

paralasys as ist prevents the neurotransmitte at he neuromuscular unction

18
Q

where are inhibitory chemical snapses motly located?

A

around cell body and axon hillock

19
Q

what is postsynaptic inhibition

A

inhibitor transmitter reduces the likelihood of an acin potentil by causing hyperpolarisation of the nerve membrane making it more negative

20
Q

what is presynaptic inhibition

A

special kind of inhibition
occurs at axo axonic axon terminals
these are terminals that are presynaptic and post syaptic
presynaptic inhibition ifs the reduction in amount of neurotransmitter relased

21
Q

where is presynaptic most common?

A

brain and spinal cord

22
Q

where are excitatory synapses located

A

dendritic tree

23
Q

where are small molecle neurotransmitters snthesised?

A

axon terminals

24
Q

why are calcium ions important to transmitter release?

A

when the presynaptic membran depolarises calcium ion voltage gated ion channels open this stmultes transmitter release.
if calcium is replaced with another ation release is blocked

25
Q

what does it mean that transmitter relase is quantial

A

small depolarisations occur with transmitter release known as mepps
when one packet of transmitter isreleased there is a uniform amplitude released when two packets are released this amplitude is doubled
it is now known that the amount o transmitter released is quantial

26
Q

what are auto receptors, where are they located and what do they regulate?

A

they are located at the presunaptic terminal sometime. they are activated with transmitter relase and regulate transmitter production

27
Q

what are ionotropic receptors and wht are their function on the post synaptic membrane?

A

they are basicallyion channel receptors
wehn the transmitter binds the channel opens letting the flow of ions into the nerve cell
action isfast an ecample is the icotinic acetylchollin receptor

28
Q

what is a metabotrophic receptor how does it work and what is its function?

A

an example is a g protein coupled receptor
works slowl as its not directly linked to an ion channel
it uses second messenger moleules such a s Cuclic amp which is part of an effector system which in turn actiates ion channels
this process is slow hich eplains the slow naure of neuro modulators

29
Q

what are the processescalled that are intiated by second messenger moleculus and how lon do the changes alst

A

the changes are usually permenant and these cascades are imporant in learning and memory
cascades can caus other effecs than just opening ion channels

30
Q

what are ther three methods of inactivation at the post snaptic membrane?

A

1diffusion
2 re uptake ie with monoamines these are reuptaken and recycled
3.enxyme breakdown

31
Q

what is aldoterone and which type of response to challenge is it ie short long or medium term

A

aldosterne encourgesretention of salt and water and is a medium term response to challenge ie blood loss in particular