NMJ Flashcards

1
Q

The resting membrane potential in a neurone is maintained predominantly

A

Leak of potassium ions out of the cell

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2
Q

What is Ach broken down into

A

Acetate and choline

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3
Q

What moves calcium back into the sarcoplasmic retinaculum

A

SERCA pumps

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4
Q

3 types of fibres

A
Slow oxidative - fatigue resistant 
fast oxidative (type A ii) 
fast glycolytic fibres ( type B)
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5
Q

what is Myasthenia gravis

A

an autoimmune disease that destroy the nAchR

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6
Q

Clinical signs of myasthenia gravis

does it get better as the day goes on ?

A

Ptosis, , Gower sign(struggle getting up) , diplopia(double vision) , slurred speech and facial paralysis

normal gets better as day goes on too

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7
Q

Treatment for Myasthenia Gravis

A

Pyridogostigmine - this inhibits AchE so there is enough Ach to bind to remaining receptors

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8
Q

What are the problems with Organophosphate poisoning - farmer

A

Inhibits AchE

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9
Q

Signs and symptoms of organophosphate poisoning

A

Increase saliva and tear production. Miosis, sweating, tremors and confusion and vomit

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10
Q

Treatment of OP poisoning

A

Atropine - blocks and bind to receptors so less Ach can bind

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11
Q

Function of Botulinum toxin

A

inhibits Ach to be released from the synaptic cleft

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12
Q

Signs and symptoms of botulinum toxin

A

Muscle paralysis, respiratory and heart failure , Dysphagia

medical uses for migraines

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13
Q

What do depolarising neuromuscular blockers do ?

A

Ach receptor agonists so bind to Each receptors and generate AP so prolonged and cannot depolarise

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14
Q

What do non-depolarising neuromuscular blockers do?

how is it treated

A

competitive antagonists so don’t let ion channels open so Ach cannot bind

treated via inhibition of AchE

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15
Q

What is a motor unit?

A

Group of muscle fibres and a single motor neurone that supplies it

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16
Q

What is the Epimysium?

and where does it come from

A

Outer layer of connective tissue that surrounds the muscle. Comes from the tendon.

17
Q

What is the Function of the Epimysium? -2

A

it allows the muscle to contract more powerfully whilst still maintaining structural integrity.
It separates muscles from other tissues allowing them to act independently.

18
Q

What are fascicles?

A

They are made up of bundles of muscle fibres(cells) - next subdivision within the muscle

19
Q

What is the connective tissue layer around the Fascicles?

And what is its function?

A

Perimysium surrounds muscle fibres

plays role in transmitting lateral contractile movements.

20
Q

What is the connective tissue around each muscle fibre? and its function( what does it contain)

A

Endomysium - this contains all the capillaries and nerves

21
Q

By what process do myoblasts differentiate into Muscle fibres

A

Myogenesis

22
Q

What are myofibrils?(actin and myosin)

A

These are fibrous proteins that make of muscle cells and they are made of thick and thin filaments

23
Q

Triad system to T tubules consist of

A

Two terminal cisternae ( release CA2+ ) and central T tubule

24
Q

When the wave of depolarisation travels along the sarcolemma what type of calcium channels are opened?

A

Voltage gated L type channels or DHPR for drugs

25
The voltage gated CA channel opens which open what kind of ligand gated calcium channel.
RYR
26
What type of troponin protein does calcium bind to?
Troponin C
27
How is calcium returned to the terminal cisternae?
SERCA pumps using energy from ATP
28
How does the depolarisation of a cardiomyocyte differ than that of a normal skeletal muscle cell?
Darker part of the cell are the intercalated discs T tubule and terminal cisternae of sarcoplasmic reticulum is shorter and forms a diad. T tubule found at level of 2 discs compared to skeletal being at A-I junction
29
Types of Leavers acronym
123 FLE
30
The arrangement of muscle fibres in fascicles contribute to the muscle force and speed. How does the length and quantity differ?
Longer and more parallel fibre arrangement = more muscle shortening ( less powerful as less fibres) e.g. sartorial Greater number of muscle fibres = greater power e.g. rectus femoris
31
Agonist
Prime mover , major force to complete movement
32
Antagonist
produce opposing force aids in controlling motion
33
Synergistic muscle actions
these types of muscles contract to prevent unwanted movements or aid the acton of the agonist
34
Duchenne muscular dystrophy is what and due to what protein degenerated what clinical sign is normally present
Muscle degeneration and weakness due to protein dystrophin that normally keeps muscle cells intact. X linked inherited degenerative disease - Gowers sign
35
what is Lambert eaton myasthenic syndrome
rare that affects the signals sent from the nerves to the muscles - muscles are unable to tighten - lung cancer autoimmune constiatipation, swallowing , dizziness and dry mouth and erectile dysfunction