BMS11004 - WEEK 3 WEDNESDAY Flashcards

synapses, gap junctions, electrical and chemical synapses, neuromuscular junctions, varieties of CNS synapses

1
Q

how can synapses enable flexible processing

A

increase complexity, and flexibility for integration (interneurons can allow multiple inputs)

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2
Q

what is strcture of electrical synapse

A

gap junctions (direct pore) allowing current to directly pass between neuron without chemicals, making cytoplasms of 2 neuron continuous

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3
Q

how large is gap junction diameter

A

1-2nm

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4
Q

how can you tell if 2 neurons are connected by gap junctions (electrical synapse)

A
  1. dye injection- small molecule so can diffuse across gap
  2. if can transmit both hyperpolarisations and depolarisations then is a electrical synapse
    if delete a connexin gene then stops as gene is required when building gap junctions
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5
Q

what are electrical synapses used for

A

reflex actions = fast communication and synchronising neurons, if necessary

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6
Q

provide overview in chemical synaptic transmissions

A
  1. package NT into vesicle, move to pre-synaptic terminal
  2. AP arrive, open v/gated Ca2+ channels
  3. Ca2+ influx cause vesicles fuse to membrane and release NT
  4. NT diffuse across synaptic cleft, activates receptor on PSC, further signalling
  5. NT removed from cleft
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7
Q

name the 2 major vesicle catagory types

A

defined by what is inside
- synaptic vesicles, dense-core secretory granules

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8
Q

compare structures of synaptic vesicles and dense-core secretory granules

A

SV = clear and small (40-50nm)
DCSG = dense and large (100nm)

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9
Q

compare what synaptic vesicles and dense-core secretory granules carry

A

SV = small molecule transmitters (eg: glutamate)
DCSG = peptide NT eg: amino acids, opioidsm endorphins

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10
Q

explain how synapic vesicle and dense-core secretory-granules are filled

A

SV = filled by presynaptic terminal transporter protein
DCSG = created and filled by ER/Golgi apparatus

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11
Q

compare lifespans for synaptic vesicles and dense-core secretory granules

A

SV = recycled via endocytosis
DGSG = one+done

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12
Q

how can you record how Ca2+ channels open

A

use calcium sensitive flurorescent proteins

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13
Q

explain how vesicles bind to membrane, using SNARE proteins (including v-SNARE, t-SNARE, synaptotagmin and “zipper”)

A

v-SNARE = vesicle
t-SNARE = target
when Ca bind to synaptotagmin, conformational change make SNAREs ‘zipper’ together and force vesicle to fuse to membrane

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14
Q

what are SNARE-proteins used for

A

targets for toxins like botulinum and tetnus
used to transport proteins around cells using their ‘zippers’

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15
Q

state 2 different ways how NT can bind to postsynaptic receptor to initiate a process

A
  1. ligand-gated ion channel
  2. G-protein coupled receptor
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16
Q

explain how NT binding to postsynaptic receptors using ligand-gated ion channels (ionotropic receptor), impacts cell

A

directly depolarises/hyperpolarises postsynaptic cell

17
Q

explain how NT binding to postsynaptic receptors using G-protein-coupled receptor (metabotropic receptors), impacts cell

A

causes biochem cascades, often involving enzymes

18
Q

what is a GPCR

A

G-protein-coupled-receptors
G proteins which are coupled to other G protein that could be responsible for multiple different effects

19
Q

name 3 methods of NT removal

A

1.diffuse away- takes time, not best way, and not temporally precise
2.actively taken up by transporters for recycling into presynaptic neuron/glia
3. destroyed in synaptic cleft by enzyme

20
Q

give properties of electrical synapses (directions, speed)

A

signal pass in both direction
passed directly and can only be attenuated (make bigger or smaller but not inverted or changed direction)
fast (<0.3ms)

21
Q

give properties of chemical synapses (directions, speed, signal transormations, modifablities)

A

signals pass in 1 direction but can be transformed to change direction, inverted, amplify
more ‘plastic’ = modifiable
slower (0.3-5ms)

22
Q

what NT do neuromuscular junctions use?

A

acetylcholine

23
Q

what are useful components of neuromuscular junctions (why may you want to use them)

A

fast and reliable, largest synapse in body, many active zones in pre-synap, junctional folds on post-syn precisely aligned to active zones = allow Ach to land exactly and definitely trigger contractions

24
Q

explain how signals in neuromuscular junctions are released in discrete amount (not in continuous amounts)

A

statistical distribution of post-synaptic potential amplitudes shows NT in “quantum packets” with 1 quantum = 1 vesicle, filled with NT
cannot release half-vesicle, but release different number of whole vesicle

25
Q

name different joinings for synapse

A
  1. axosomatic = soma
  2. axodendritic = dendrites
  3. axoaxonic = one terminal button onto another
  4. axospinous = presynaptic neurons onto post-dendritic spine
  5. dendrodentric = dendrites form synapse with others
  6. dendrosomatic = dendrite onto somas
26
Q

explain how botulinum toxin causes paralysis

A

targets SNARE proteins, ‘zippers’ for movement of NT
so cannot move chemicals into vesicle for synaptic transmissions

27
Q
A