Structure of a chemical synapse in the brain: pre and post synaptic mechanisms (Dr. Edwards) Flashcards

1
Q

Do dendrites always project on one side of the axon ?

A

Not at all. There can be basal dendrites as well.

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

How many axons leave the soma ?

A

ONE, and only ONE.

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

What are two types of cells that illustrate the dendritic heterogeneity in neurons ?

A

Parking cells of the cerebellar cortex are very arborated on one side of the soma and on the other side a single axon carries the info to the presynaptic terminal.
Pyramidal neurons in the neocortex generally have less branched dendrites, which are both apical and basal.

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

How bing is the axon compared to the dendrites ?

A

The axon is usually longer (but very variable, 10μs-meters) and thinner than dendrites (again, thickness varies depending on myelination) whilst dendrites tend to be shorter (10-100μms) and tapering.

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

How is communication w/in and between 2 or more neurons different ?

A

Communication w/in one given neuron travels as an “all or none” AP.
Communication from one neuron to another occurs in the form of a graded potential, a PSP (Post Synaptic Potential).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How wide is the synapse ?

How long is the synaptic divide ?

A

About 1 μm, can be smaller.

Between 15-40nm.

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

What are the main types of receptors on a postsynaptic neuron ?

A

AMPA (α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid) receptors/channels, NMDA (N-methyl-D-aspartate) receptors/channels, kainate receptors, metabotrobic receptors, but also AMPA quantal clusters (ask Dr. Edwards).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

On which side of the synapse are there more mitochondria ?

Why ?

A

The presynaptic side.

Mitochondria are important for clearing calcium from the synaptic terminal.

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

What is the active zone ?

A

Site of neurotransmitter release.

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

What is the PSD (Post Synaptic Density) ?

A

The PSD is a protein dense specialization attached to the postsynaptic membrane. PSDs were originally identified by electron microscopy as an electron-dense region at the membrane of a postsynaptic neuron.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the main proteins involved in neurotransmitter release ?

A

The SNARE proteins: v-SNAREs and t-SNAREs, synaptotagmins, and synapsins.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are the different kinds of SNARE proteins ?

A

v-SNARE is associated w/ the vesicle (synaptobrevin is part of this sub-family)
t-SNARE is associated w/ the membrane
SNAP-25/synapsin complex = t-SNARE complex

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

Where is synaptotagmin and what does it do ?

A

It is a vesicle associated protein that binds calcium to trigger neurotransmitter release.

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

What are synapsins and what do they do ?

A

Synapsins are a family of proteins that bind synaptic vesicles to components of the cytoskeleton which prevents them from migrating to the presynaptic membrane and releasing neurotransmitter.
Upon phosphorylation, synapsins release the vesicles.

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

Describe one theory explaining the mechanism of neurotransmitter release ?

A

Once calcium ions bind to synaptotagmin, the t-SNAREs and v-SNAREs bind and “zip” together about halfway through. This forms the 7S complex.
Synaptotagmin then binds this structure w/ SNAP and NSF (N-ethylmaleimide Sensitive Fusion) protein to form the 20S complex. Upon hydrolysis of ATP to ADP, the SNAREs completely “zip together” so that the vesicle fuses totally w/ the membrane and its neurotransmitter is released into the cleft.

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

How big are vesicles and in what concentrations are neurotransmitters present in them ?

A

Vesicles have a aprox a 35-50nm diameter and contain about 100mM of neurotrsmitter, which represents about 2000 molecules.

17
Q

What is the concentration of neurotransmitter released into the cleft ?
How quickly does the neurotransmitter travel the cleft space ?

A

Neurotransmitter is present in the cleft at a 1mM concentration. It travels the cleft space in 1ms.

18
Q

What is the role of the NMDAR ?

A

It is a coincidence ionotropic receptor, detecting the coincidence of glutamate (or glycine) release due to presynaptic depolarization and postsynaptic depolarization (from any source).
It is blocked by a magnesium ion and can only open when the EPSP reaches about 0mV, thus becoming permeable to Ca2+ and monovalent cations.

19
Q

What is the difference between ionotropic and metabotropic receptors ?

A

Ionotropic receptors form an ion channel pore. In contrast, metabotropic receptors are indirectly linked with ion channels on the plasma membrane of the cell through signal transduction mechanisms (often G proteins). Hence, GPCRs are inherently metabotropic.
Ionotropic receptor are much faster (<1ms) than second messenger systems (>50ms-seconds), but the latters can be more regulated.

20
Q

What are the three types of ionotropic glutamate receptors ?

A

AMPA, kainate and NMDA receptors.

21
Q

What are the agonists and antagonists of AMPA and kainate ionotropic receptors ?
What are these channels permeable to ?

A

agonists: glutamate, AMPA
antagonists: CNQZ, NBQX etc
These receptors are permeable to monovalent cations only (and sometimes a little bit to Ca2+ as well)

22
Q

What are the agonists and antagonists of the NMDA ionotropic receptors ?
What are NMDARs permeable to ?

A

agonists: Glu (+ Gly), NMDA, aspartate
antagonists: APV, 7CL-Kynurenate etc.
These channels are permeable to Ca2+ and monovalent cations.

23
Q

Why do we often say that NMDARs are not dependent on glycine release ?

A

NMDARs need occupation of both binding to Glu and a Gly binding site for activation, but the Gly site is very high affinity. Normally, enough Gly is present extrasynaptically to saturate this site. That is why NMDARs are not dependent on Gly release.

24
Q

What is the mGluR ?

A

A metabotropic Glu receptor.

25
Q

What receptors does nicotine bind ?

A

The nicotinic ionotropic receptor and the muscarinic metabotropic receptor.

26
Q

What receptors does ATP bind to ?

A

The P2X ionotropic receptor and the P2Y metabotropic receptor.

27
Q

What receptors does GABA bind to ?

A

The GABA(A) ionotrobic receptor and the GABA(B) metabotropic receptor.

28
Q

What recetpors does Gly bind to ?

A

The glycine ionotropic recepor.

NO metabotrobic receptor known (yet).

29
Q

What are the respective effects of monovalent cation and anion influx on the RMP ?

A

Monovalent cation influx produces an EPSP (RMP rises towards the E of Na+ which is about +60mV, only reaches +40mV max).
Monovalent anion produces an IPSP (decreases towards E of Cl- around -85mV).