Lecture 5 Flashcards

1
Q

What is synaptic transmission?

A

Transfers information at a synapse
- named by Charles Sherrington

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2
Q

What’s the direction of information transfer?

A

Neuron to target cell
- Presynaptic neuron to postsynaptic neuron

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3
Q

What are the 2 types of synapses?

A

Electrical and Chemical Synapses

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4
Q

What are gap junctions made of?

A

connexin proteins formed by 6 connexins

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5
Q

What are cells electrically coupled?

A

flow of ions from cytoplasm of one cell to the cytoplasm of another cell

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6
Q

How do electrical synapses differ from chemical ones?

A
  • bidirectional
  • fast transmission (postsynaptic potentials)
  • multiple PSPs occur at the same time to excite a neuron (cause action potential)
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7
Q

What are the 5 synaptic arrangements in the CNS?

A
  • axodendritic: axon to dendrite
  • axosomatic: axon to cell body
  • axoaxonic: axon to axon
  • axospinous: axon to dendritic spine
  • dendrodenritic: dendrite to dendrite
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8
Q

What is Gray’s type I morphology?

A

asymmetrical, excitatory synapses
- Glutamate neurotransmitterW

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9
Q

What is Gray’s type II morphology?

A

symmetrical, inhibitory synapses
- GABA or glycine neurotransmitter

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10
Q

What’s the purpose of the neuromuscular junction?

A

studies of this established the principles of synaptic transmission

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11
Q

What is the neuromuscular junction made of?

A

junctional folds with numerous neurotransmitter receptors

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12
Q

How do chemical synaptic transmissions work?

A

1) Neurotransmitter synthesis
2) Load neurotransmitter into synaptic vesicles
3) Vesicles fuse to presynaptic terminal
4) neurotransmitter spills into synaptic cleft
5) Binds to postsynaptic receptors
6) Biochemical/electrical response elicited in postsynaptic cell
7) removal of neurotransmitter from synaptic cleft

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13
Q

What are the 3 groups of neurotransmitters with an example?

A

Amino acids: small organic molecules - vesicle (GABA)
Amines: small organic molecules - vesicles (dopamine)
Peptides: short amino acid chains - secretory granules (dynorphin)

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14
Q

What are secretory granules made of?

A

peptide neurotransmitter at the soma by the rough ER (golgi apparatus pathway)
- sent to presynaptic sites by microtubule transport

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15
Q

What do synaptic vesicles require?

A

Neurotransmitter synthesizing enzyme and vesicular neurotransmitter transport protein

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16
Q

What is docking of synaptic vesicles mediated by?

A

v-SNARES and t-SNARES proteins

17
Q

What causes exocytosis?

A

Increase in intracellular calcium
Ca++ binds to calcium sensor proteins (Synaptotagmin) and alters conformation of SNARE complexes, triggering vesicle membrane incorporation into presynaptic membrane
Neurotransmitter released into cleft
Vesicle membrane recovered by endocytosis

18
Q

What are examples of neurotransmitter receptors?

A

Transmitter-gated ion channels
Metabotropic Receptors
G-protein coupled receptors

19
Q

Contrasts EPSP and IPSP.

A

EPSP = Excitatory Post-Synaptic Potential
- transient postsynaptic membrane depolarization caused by presynaptic release of neurotransmitter
- EPSPs added together to produce significant, postsynaptic depolarization
- Threshold can be reached to fire action potential after integration

IPSP = Inhibitory Post-Synaptic Potential
- Transient hyperpolarization of postsynaptic membrane potential caused by presynaptic release of neurotransmitter

20
Q

What causes generation of an EPSP?

A

Neurotransmitter (usually glutamate) and Glutamate ion channels like AMPA, NMDA

21
Q

How do you quantitatively measure EPSPs?

A

Synaptic vesicles: elementary units of synaptic transmission
Quantum: invisible unit
Quantal analysis: used to determine number of vesicles that release during neurotransmission

22
Q

What are some important dendritic properties?

A

Many have voltage gated channels
They contribute to more complex integrative properties
Membrane depolarization falls off exponentially with increasing distance along a dendrite

23
Q

How do different EPSP summations affect the graph?

A

Spatial summation = high peak on action potential
Temporal summation = little bumps upwards

24
Q

What’s the point of EPSP summation?

A

allows for neurons to perform sophisticated computations

25
Q

How do excitatory and inhibitory synapses differ?

A

They bind different neurotransmitters, allowing different ions to pass through channels

26
Q

When will IPSP have hyperpolarizing effect?

A

when membrane potential is less negative than -65 mV

27
Q

What is shunting inhibition?

A

Synapse inhibits current flow from soma to axon hillock

28
Q

What are autoreceptors?

A

Presynaptic receptors sensitive to the neurotransmitter released by the presynaptic terminal

29
Q

What is the function of autoreceptors?

A

Safety valve
- common effect is inhibition of neurotransmitter release

30
Q

What are the possible fates of synaptic released neurotransmitters?

A
  • diffusion of transmitter molecules away from the synapse
  • reuptake: neurotransmitter re-enteres presynaptic axon terminal (requires plasma membrane transport proteins)
  • uptake by nearby glia cells AKA astrocytes (requires plasma membrane transport proteins)
  • enzymatic degradation
31
Q

What is neuropharmacology?

A

study of effect of drugs on the nervous system

32
Q

What are receptor antagonists?

A

inhibitors of neurotransmitter receptors
ex. curane

33
Q

What are receptor agonists?

A

mimic actions of naturally occurring neurotransmitters
ex. nicotine

34
Q

How does drug addiction work molecularly?

A

destroys brain reward circuits