M6 L4 : Synaptic transmission Flashcards

1
Q

What is synaptic transmission

A

the process of transferring information between neurons (through axodendritic synapse) or between neurons and muscle fibres (neuromuscular junction=endplate)

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2
Q

What are the two ways synaptic transmission occurs and where are they most likely

A

Chemical synapses (neurons in the brain as well as in endplates) and electrical synapses (via pores called gap junctions)

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3
Q

What are the three key features of chemical synapses

A
  • SPECIFICITY (specific neurotransmitters have specific effects on the post synaptic membrane.
  • COMPLEXITY: type, time course, strength, location
  • PLASTICITY : changes in synaptic structure and function associated with development aging and learning
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4
Q

Describe the stages of excitatory synaptic transmission in neuromuscular junction

A
  1. Presynaptic action potential triggers voltage gated Ca+ channels to open, Pca+ increases with Ca+ influx.
  2. Transmitter : ACh is released by exocytosis which diffuse over the synaptic cleft
  3. ACh binds to post synaptic receptors which activate ligand gated ion channels- non selective to both NA+ and K+ sometimes Ca2+
  4. This always shifts RMP from -65 to toward threshold for AP (-55mV). This is End plate potential.
  5. Once triggered AP is transmitted along muscle fibre by passive spread.
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5
Q

How long is the synaptic delay between the first AP in presynaptic neuron and second AP in postsynaptic neuron

A

half a millisecond

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6
Q

Why does the EPP always depolarise and trigger Excitatory Post Synaptic Potential (EPSP)

A

non selective cationic channel means that membrane potential will be somewhere between equilibrium potential for both (-80mV for K+ and +60 mV for Na+ ) so it will be closer to 0, definitely higher than 55

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7
Q

What are the two main types of chemical synpases in the CNS and how do they effect the Post synaptic membrane

A

Excitatory Post synaptic potentials (EPSP) which DEPOLARISE the psm and Inhibitory postsynaptic potentials (IPSP) which HYPERPOLARISE the psm.

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8
Q

What are the main neurotransmitters related to ESPS and what is the ionic mechanism

A
Glutamic acid (glutamate) in the brain or Acetylcholine. 
ionic mechanism is transient opening of Na+K+ and sometimes Ca2+ channels
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9
Q

What are the main neurotransmitters related to ISPS and what is the ionic mechanism

A

GABA (gamma-aminobutyric acid) or glycine
Ionic mechanism: transient opening of ligand gated K+ channels. This shifts RMP towards equilibrium potential of K+ (-80mV) and therefore away from threshold.

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10
Q

What are the two classifications of neurotransmitters (based on chemical structure)

A

Small molecule neurotransmitters (classical) and Neuropeptides (neuromodulators stored in presynaptic vesicles)

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11
Q

What are examples of small molecule transmitters and general speed and direction

A

Usually fast action and direct on postsynaptic receptors

Eg: Amino acids (glutamate, GABA, glycine), ACh, Biogenic Amines: (serotonin, noradenaline and dopamine)

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12
Q

What are neuropeptides, their general speed and direction as well as examples

A

Large molecule chemicals that have an indirect (metabotropic) action on post synaptic receptors or modulatory action on the effects of other neurotransmitters.
Slow (seconds to minutes) , direction is more diffusing rather than direct.
Dozens of neuropeptides identified Eg. Neuropeptide Y, Substance P, Kisspeptin, Enkephaln.

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13
Q

What are the three factors determining synaptic action relating to neurotransmitter and channel action

A
  1. the type of neurotransmitter released
  2. The type of neurotransmitter receptor/channel complex expressed in the post synaptic membrane
  3. The amount of neurotransmitter receptor present in the post synaptic membrane (synaptic plasticity : Long term potention or depression.
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14
Q

Define synaptic plasticity

A

synaptic basis for memory formation: more receptors or less for long term potention or long term depression

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15
Q

Why can one receptor initiate more than one type of response

A

many transmitters bind to more than one type of receptor (eg. Glutamate binds to AMPA, NMDA, and Kainate) and the response varies depending on the type of receptor that transmitter binds to,increasing the information handling capacity of neurons

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16
Q

What are the two types of mechanism used to gate ion channels by transmitters and which class of neurotransmitter are they related to

A

Direct gating: fast and short lasting direct binding to ion channel is for classical neurotransmitter

Indirect gating: neuropeptidestransmitter binds to receptors : GPCR that activate G protein. which bind GTP. 2nd messengers are produced which activate protein kinase which phosphorylate ion channels and this causes them to open close slower and longer lasting.

17
Q

How are neurotransmitters inactivated and why is this important

A
  1. diffusion away from the synapse (little)
  2. enzymatic degradation in the synaptic cleft (main)
  3. Re uptake and recycling which involves specific active neurotransmitter transporters in the presynaptic membrane that
18
Q

What are the enzymes that break down ACh, biogenic amines and neuropeptides

A

Acetylcholinesterase; monoamine oxidase for biogenic amines; peptidases for neuropeptides

19
Q

Why is integration of synaptic neurons needed

A

each neuron receives thousands of synapses E and I but each only produces a small 0.1mV at the axon initial segment and decay when they are passively conducted from dendrites.
In order to depolarise the intial segment ot threshold (15mV) EPSPS need to be enhanced

20
Q

What are the two types of temporal and spatial summation of post synaptic potentials at axon initial segment that result in threshold

A

2 post synaptic potentials occur at one excitatory synapse, 2nd coming before the first has finished. (temporal summation) and two coming at the same time (spatial summation) from two excitatory synapses

21
Q

What are the two types of temporal and spatial summation of post synaptic potentials at axon initial segment that result in the threshold not being reached

A

two ESPS coming in one after the other has finished and spatial summation of EPSP and IPSP which balances out the depolarisatoin with a hyperpolarisation.

22
Q

What is excitotoxicty

A

Too much glutamate release or insufficient reuptake leads to an excessive activation of neurons through the NMDA and AMPA/Kainate receptors. Large Ca2+ influx assocated with over activation of NMDA receptors causes neuron damage= excitoxicity. Seen in stroke, epilepsy, brain injury.

23
Q

What are the four types of recpetors that glutamate binds to which causes EPSP

A

3 directly gated : AMPA, NMDA and Kainate and 1 indirectly gated (Metabotropic glutamate receptor)