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
Q

The voltage gated CA channel opens which open what kind of ligand gated calcium channel.

A

RYR

26
Q

What type of troponin protein does calcium bind to?

A

Troponin C

27
Q

How is calcium returned to the terminal cisternae?

A

SERCA pumps using energy from ATP

28
Q

How does the depolarisation of a cardiomyocyte differ than that of a normal skeletal muscle cell?

A

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
Q

Types of Leavers acronym

A

123 FLE

30
Q

The arrangement of muscle fibres in fascicles contribute to the muscle force and speed. How does the length and quantity differ?

A

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
Q

Agonist

A

Prime mover , major force to complete movement

32
Q

Antagonist

A

produce opposing force

aids in controlling motion

33
Q

Synergistic muscle actions

A

these types of muscles contract to
prevent unwanted movements
or aid the acton of the agonist

34
Q

Duchenne muscular dystrophy is what and due to what protein degenerated

what clinical sign is normally present

A

Muscle degeneration and weakness due to protein dystrophin that normally keeps muscle cells intact.

X linked inherited degenerative disease - Gowers sign

35
Q

what is Lambert eaton myasthenic syndrome

A

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