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Communication via Synapses Communication via Synapses

Communication via Synapses - PowerPoint Presentation

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Communication via Synapses - PPT Presentation

Synapses are a fundamental part of neural pathways as they regulate decisionmaking in terms of exciting or inhibiting the postsynaptic neurons Review Action potentials AP reach terminal bud of the presynaptic neuron ID: 261329

post synaptic nts dopamine synaptic post dopamine nts neuron action excitatory inhibitory potential axon depolarisation threshold neurotransmitters propagated cocaine

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Slide1
Slide2

Communication via Synapses

Synapses are a fundamental part of neural pathways as they regulate decision-making in terms of exciting or inhibiting the post-synaptic neurons.

Review:

Action potentials (AP) reach terminal bud of the pre-synaptic neuron.

Neurotransmitters (NT), chemical messengers, diffuse across the synapse to bind with receptors on the post-synaptic membrane.

Neurotransmitters

are:

Excitatory

, which means they excite the post-synaptic neuron (contributing to

depolarisation

and propagation of the AP.

OR:

Inhibitory

,

hyperpolarising

the post-synaptic neuron and preventing AP. Slide3

Neurotransmitters

can be

excitatory

or

inhibitory

Neurotransmitters

(NT) are proteins

diffuse across the synaptic cleftbind with a receptor on the post-synaptic neuron.Whether or not the post-synaptic neuron propagates the action potential depends on: Which NT diffuses acrossWhich receptors they bind toWhich ions flow in/out of the post-synaptic neuronWhether or not depolarisation reaches threshold

-70mv

0mv

time

threshold

resting

depolarisation

hyperpolarisation

Excitatory NTs cause

depolarisation

e.g.

ACh

, dopamine

NT binds, Na+ channels open, Na+ rushes in

Membrane potential

depolarises

, AP propagated

Inhibitory NTs cause

hyperpolarisation

e.g. GABA, dopamine (on different pathways)

NT binds to receptor

K+ channels open, K+ rushes out

OR

Cl

- channels open,

Cl

- rushes in

Membrane potential become more negative

Action potential is prevented from propagatingSlide4

This is a useful example of an inhibitory neurotransmitter.

http://

www.youtube.com

/

watch?v

=-pfG6yHAQ5USlide5

Decision-making in the Central Nervous System (CNS)

axon

synapse

axon hillock

action potential

The axons of

many

pre-synaptic neurons feed into the dendrites of one post-synaptic neurons via synapses.

The ‘decision’ whether or not to propagate

the action potential along the axon of the

post-synaptic neuron takes place

in a region of the cell body

called the

axon hillock

.

This is achieved through

summation

of the incoming impulses. If the total

impulse reaches

threshold

,

the post-synaptic neuron

depolarises

and

the action potential is propagated.

If the sum does not reach threshold, the AP is not propagated.

There are two main methods of summation:

temporal

and

spatial

.

Slide6

Decision-making in the Central Nervous System (CNS)

Temporal summation

Action potentials arrive in rapid succession

Depolarisation

in the axon hillock is summative

If it reaches threshold before

repolarisation

, the AP is propagated.

Spatial summation

Action potentials arrive simultaneously from multiple sources

Some neurotransmitters are excitatory (increasing

depolarisation)

Other NTs are inhibitory (hyperpolarising). Summation in the axon hillock is summative.

If it reaches threshold the AP is propagated. Slide7

How do psychoactive drugs affect the brain?

Before thinking about how drugs affect the synapses, be sure you understand how they work and are reset.

Some NTs have a normal excitatory function

Other NTs have a normal inhibitory function

In general, psychoactive drugs can:

Increase or

decrease the release of NTs (e.g. THC – cannabis)

Breakdown re-uptake proteins which are responsible for returned used components of NTs to the pre-synaptic neuron (ready to use again)Block re-uptake proteins (e.g.cocaine)Mimic or block NTs, binding to the receptors on post-synaptic membranesInhibit production of new NTsSlide8
Slide9

Excitatory drugs

increase post-synaptic transmission

Examples:

Nicotine, amphetamines,

cocaine

What is the effect of cocaine?

Normal:

Dopamine acts as excitatory NTDopamine is re-uptaken by pumps on the pre-synaptic membrane. With Cocaine:Cocaine blocks re-uptake pumpsDopamine remains in synaptic cleft

More dopamine continues to be releasedSummative increase in post-synaptic transmissionEffects on mood:

Dopamine is involved in reward pathways, enhancing feelings of pleasureLonger-lasting feelings as dopamine is not re-uptaken

Effects on behaviour:

feelings of euphoriaincreased energy and alertnesshighly addictive

association with depression as body reduces production of own dopamine over timeSlide10

Inhibitory drugs

decrease

post-synaptic transmission

Examples:

Alcohol,

benzodiazapines

, THCWhat is the effect of tetrahydrocannibol (THC)? Normal: Dopamine release is moderated (inhibited) by GABAWith THC:THC mimics cannabinoids and inhibits

GABA release by binding to cannabinoid receptorsGABA cannot inhibit dopamine releaseMore dopamine is released

Effects on mood: Dopamine is involved in reward pathways, enhancing feelings of pleasure

Not as extreme release of dopamine as with cocaine, but still higher than normalEffects on behaviour

:intoxicationhunger

memory impairmentpotential dependencySlide11
Slide12

http://

www.youtube.com

/

watch?v

=bCChf2WHNE4Slide13
Slide14
Slide15
Slide16