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Starter Questions - PowerPoint Presentation

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Starter Questions - PPT Presentation

Following a stimulus explain how the opening of sodium ion channels affects the potential difference across a neurone cell membrane Describe and explain the movement of sodium ions if the potential difference across a neurone cell membrane reaches the threshold level ID: 261323

action sodium channels neurotransmitter sodium action neurotransmitter channels potential neurone membrane ions ion synaptic acetylcholine postsynaptic summation step open threshold cleft calcium

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Slide1

Starter Questions

Following a stimulus, explain how the opening of sodium ion channels affects the potential difference across a neurone cell membrane.

Describe and explain the movement of sodium ions if the potential difference across a neurone cell membrane reaches the threshold level.

Describe the structure of a militated neurone. Slide2

Answers

Sodium ions diffuse into the neurone down the sodium ion electrochemical gradient. This makes the inside of the neurone less negative and so decreases the potential difference across the membrane.

More sodium ions diffuse into the neurone because more sodium ion channels open.

A

myelinated

neurone has a myelin sheath. The myelin sheath is made of a type of cell called a

schwann

cell. Between the

schwann

cells are tiny patches of bare membrane called the nodes of

ranvier

. Sodium ion channels are concentrated at the nodes of

ranvier

. Slide3

http://www.youtube.com/watch?v=LT3VKAr4rooSlide4

Synapses

The Basic Idea

Synapses are gaps between neurones

Information is sent between neurones by chemical transmission

Neurotransmitters pass across the synaptic cleft

A new action potential will be triggered in the post synaptic neurone Slide5

The synapse

Where two neurones meet, there is a gap, usually about 20nm wide. This is the

synaptic cleft

The end of the neurone immediately before the synaptic cleft, ends in a

presynaptic

bulb.After the synaptic cleft is the postsynaptic bulb, i.e. the start of the next neurone Together they make up the synapseSlide6

Structure of the synapseSlide7

Neurotransmitters

There are more than 40 different neurotransmitter substances.

Noradrenalin

and

acetylecholine

(ACh) are found throughout the nervous systemDopamine and glutamate are found only in the brain.Synapses releasing achetylcholine and known as cholinergic synapses Slide8

Postsynaptic Neurone

Presynaptic Neurone

Synaptic

Cleft

Synaptic

Knob

Calcium ion channel

Sodium ion channels

Membrane of postsynaptic neurone

Synaptic vesicle containing neurotransmitter

Smooth Endoplasmic Reticulum

Mitochondrion

Incoming

Action PotentialSlide9

Incoming

Action Potential

New action Potential

NeurotransmitterSlide10
Slide11

Step 1 – Calcium Channels Open

The incoming action potential causes depolarisation in the synaptic knob

This causes calcium channels to open

Calcium ions (Ca

2+

) flood into the synaptic knobSlide12

Incoming

Action Potential

Ca

2+

Ca

2+

Ca

2+

Ca

2+Slide13

Step 2 – Neurotransmitter Release

The influx of calcium ions causes synaptic vesicles to fuse with the presynaptic membrane

This releases neurotransmitter in to the cleft

So calcium ions cause the release of neurotransmitterSlide14

Incoming

Action Potential

Ca

2+

Ca

2+

Ca

2+

Ca

2+Slide15

Step 3 – Sodium Channels

Neurotransmitter (acetylcholine) is released into the synaptic cleft.

Acetylcholine binds to the receptor site on the sodium ion channels.

Sodium ion channels openSlide16

Ca

2+

Ca

2+

Ca

2+

Ca

2+

Neurotransmitter (acetlycholine) is released into the synaptic cleft. Acetlycholine binds to the receptor site on the sodium ion channels.Slide17

Sodium Channels

The sodium channels on the postsynaptic membrane are normally closed.

When the neurotransmitter binds there is a conformational change opening the channel.

This allows sodium ions to flood in and causes depolarisation.

Neurotransmitter binds and opens the channel.

Na

+Slide18

Sodium ions diffuse into the postsynaptic neurone

Depolarised

Empty Synaptic VesiclesSlide19

Step 3 – Sodium Channels

Neurotransmitter (acetylcholine) is released into the synaptic cleft.

Acetylcholine binds to the receptor site on the sodium ion channels.

Sodium ion channels open

Sodium ions diffuse in (down steep concentration gradient)

Postsynaptic neurone depolarisesSlide20

Step 4 – New Action Potential

Depolarisation inside the postsynaptic neurone must be above a threshold value

If the threshold is reached a new action potential is sent along the axon of the post synaptic neuroneSlide21

Incoming

Action Potential

New action Potential

NeurotransmitterSlide22

Questions

When do the calcium channels open and close?

Why are the calcium ions important?

What is the name of the neurotransmitter?

Explain how the neurotransmitter causes a new action potential to be generated.Slide23

The rest of the process

Step 1 Calcium channels open

Step 2 Neurotransmitter release

Step 3 Sodium Channels

Step 4 New action potential

Step 5 AcetylcholinesteraseStep 6 Remaking acetylcholineSlide24

Step 5 Acetylcholinesterase

A hydrolytic enzyme

Breaks up acetylcholine (the neurotransmitter) into acetyl (ethanoic acid) and choline.Slide25
Slide26

Acetylcholinesterase

Acetylcholinesterase is an enzyme that hydrolyses acetylcholine in to separate acetyl (ethanoic acid) and choline.

Sodium ion channels close.

The two bits diffuse back across the cleft into the presynaptic neurone.

This allows the neurotransmitter to be recycled.Slide27

Acetylcholine binds and opens Sodium channels

Acetylcholinesterase breaks up acetylcholine. Sodium channels close

DepolarisedSlide28

Why break down acetylcholine?

If the neurotransmitter is not broken down this could allow it to continuously generate new action potentials

Breaking down acetylcholine prevents thisSlide29

Questions

Name the hydrolytic enzyme and the products of the reaction.

Why must the neurotransmitter be broken down?

What happens to the remnants of the neurotransmitter?Slide30

Step 6 Remaking Acetylcholine

ATP released by mitochondria is used to recombine acetyl (ethanoic acid) and choline thus recycling the acetylcholine.

This is stored in synaptic vesicles for future use.

More acetylcholine can be made at the SER.

Sodium ion channels close in the absence of acetylcholine at their receptor sites.

The synapse is now ready to be used again.Slide31

The Whole ProcessSlide32

Incoming

Action Potential

Ca

2+

Ca

2+

Ca

2+

Ca

2+Slide33
Slide34
Slide35

Neuromuscular Junctions

A neuromuscular junction is a specialised cholinergic between a motor neurone and a muscle cell. Neuromuscular junctions use the neurotransmitter acetylcholine (Ach), which binds to cholinergic receptors called nicotinic cholinergic receptors. Slide36

Very similar to Cholinergic synapses with a few differences

Postsynaptic membrane has lots of folds that form clefts. These clefts store the enzyme that breaks down Ach (

acetylcholinesterase

)

Postsynaptic membrane has more receptors than other synapses

Motor neurone fires an action potential, it always triggers a response in a muscle cell. This isn't always the case for a synapse between two neurones. Slide37

Excitatory and Inhibitory Neurotransmitters

Excitable neurotransmitters depolarise the postsynaptic membrane.

E.g.Acetylcholine

.

Inhibitory neurotransmitters e.g. GABA is an inhibitory neurotransmitter, when it binds to its receptors it causes potassium ion channels to open on the postsynaptic membrane, hyperpolarising the neurone. Slide38

Summation

Low frequency action potentials often release insufficient amounts of neurotransmitter to exceed the threshold in the postsynaptic neurone

Summation allows action potentials to be generated

This enables a build up of neurotransmitter in the synapseSlide39

Spatial Summation

A number of different presynaptic neurones share the same synaptic cleft

Together they can release enough neurotransmitter to create an action potential

Multiple neuronesSlide40

Below the thresholdSlide41

Spatial Summation

Threshold reached action potential can be sentSlide42

Temporal Summation

A single presynaptic neurone releases neurotransmitter many times over a short period

If the total amount of neurotransmitter exceeds the threshold value an action potential is sent

1 neuroneSlide43

Temporal Summation

Low frequency action potentialsSlide44

Temporal Summation

High frequency action potentialsSlide45

Questions

What is summation?

What is the main difference between temporal summation and spatial summation?

Explain how temporal summation allows the postsynaptic membrane to reach the threshold value.

Suggest an advantage of responding to high-level stimuli but not low-level ones.Slide46

Inhibition

There are chloride ion channels on the postsynaptic membrane

If these are made to open chloride ions (

Cl

-

) flood into the postsynaptic neuroneThis hyperpolarises the neuroneThis make it harder to achieve a action potentialSlide47

Chloride ion (

Cl

-

)channel on the postsynaptic membrane

Neurotransmitter that opens calcium channelsSlide48

Chloride ions diffuse into the postsynaptic neurone

HyperpolarisedSlide49

Summation & Inhibition

Inhibitory and excitatory neurones will work antagonistically at the same synapse

Summation will occurSlide50

Exam Questions 1a

1.

(a) (

i

)

A Three marks for three of:Negatively charged proteins / large anions inside axon;Membrane more permeable to potassium ions than tosodium ions;Potassium ions diffuse* out faster than sodium ions diffuse in;Sodium / potassium pump;Sodium ions pumped* out faster than potassium ions pumpedin / 3 for 2; [3 max]* mechanism is necessary for mark Slide51

Exam Questions 1b

B

Sodium ion gates open / membrane more permeable to

sodium ions / sodium ions rush in; [1]

(ii) Two marks for two of:Membrane impermeable to sodium ions / sodium ion channels closed;Sodium ions cannot enter axon;Membrane becomes more negative than resting potential; [2 max] (b) (i) Two marks for two of:Unique shape of receptor protein / binding site; reject ‘active site’Due to (tertiary) structure of protein molecule;Concept of complementary shape / ref. to neurotransmitter ‘fitting’; [2 max]

(ii) Cause vesicles to move to

pres

ynaptic membrane /

fuse with membrane; [1]

Slide52

Exam Questions 1c

(c) (

i

)

Two marks for two of:

Impulses / action potentials from neurones A and B together /spatial summation;Cause sufficient depolarisation / open sufficient sodium ion channels;For threshold to be reached; [2 max] (ii) Two marks for two of:Impulses from A and B independent / no summation;Threshold not reached;Insufficient sodium ion channels opened; [2 max] (iii) Inhibitory;More IPSPs than EPSPs / reduces membrane potential / makes morenegative (allow hyperpolarisation) / cancels effect of action potentialfrom A; [2 max]Slide53

Exam Questions 2a

2.

(a) Initially membrane impermeable to Na+;

Sodium channels open;

allowing Na+ into axon;

reverses potential difference across membrane/ charge on either side/depolarised;membrane becomes more permeable to K+ ions/K+ leave the axon; [max. 4]Slide54

Exam Questions 2b

(

i

) All action potentials are the same size;

threshold value for action potential to occur [2]

(ii) frequency of action potentials [1] several (sub-threshold) impulses add to produce an action potential [1]Slide55

Drugs at Synapses

Drugs can affect the synaptic transmission. They can do this by various ways. E.g. Some drugs are the same shape of neurotransmitters so they mimic their action at receptors (Agonists)

Example: Nicotine mimics acetylcholine so binds to nicotinic cholinergic receptors in the brain.