Neuromuscular Junction Lecture Flashcards

1
Q

What is the neuromuscular junction?

A

It is the site of regulation of skeletal muscle by the nervous system

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2
Q

How many neuromuscular junctions are generally on a skeletal muscle cell?

A

Just one

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3
Q

Give me the sequence of events from an action potential in a motor neuron to an action potential in the sarcomolemma of a muscle cell.

A
  1. AP travels along the motor neuron axon
  2. AP invades the presynaptic terminal
  3. Ca++ influx occurs in the presynaptic terminal
  4. Vesicles carrying ACh are released into the synaptic cleft
  5. ACh diffuses across the cleft
  6. ACh binds to its receptors in the postsynaptic membrane
  7. Na+ and K+ channels open and there is an influx of Na+ and an efflux of K+ across the motor endplate
  8. An endplate potential is generated
  9. Voltage gated Na+ channels in the sarcolemma open and an action potential is initiated in the sarcolemma.
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4
Q

T/F the end plate potential is an all or none amplitude?

A

False- they are graded, don’t propagate, and can undergo summation

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5
Q

When do end plate potentials occur?

A

After an action potential in a motor neuron

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6
Q

What are mini endplate potentials? (MEPPs)

A

They are spontaneous end plate potentials that are really small- 1-2 mV

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7
Q

If acetylcholinesterase wasn’t present in the motor endplate membrane and the basal lamina of the muscle cell, what would happen?

A

Well, the muscle would undergo continuous contraction. AChesterase serves to break down the ACh in the synaptic cleft so that stimulation occurs only at the proper time

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8
Q

Pharmacology- what does curare do to the NMJ?

A

It binds to ACh receptors so that ACh can’t bind. No action potentials can occur

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9
Q

Pharmacology- what does Botulinum toxin do to the NMJ?

A

This blocks ACh release

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10
Q

Pharmacology- what do organophosphates do to the NMJ?

A

These block the action of AChEsterase so that it won’t be hydrolyzed

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11
Q

How is skeletal muscle organized, from smallest component to largest?

A

Protein–> filaments–>sarcomere–>myofibril–>muscle fiber (cell)–>fascicle–> whole muscle

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12
Q

Each strand tropomyosin is composed of what?

A

a dimer of tropomyosin

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13
Q

Tropomyosin sits where?

A

In the grooves of the actin filaments

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14
Q

Troponin has how many subunits? What is each responsible for?

A

3
TnC- calcium binding
TnI- inhibitory role
TnT- tropomyosin binding - anchors the whole molecule

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15
Q

Tell me about the myosin filament/molecules.

A

Well, the myosin filament is thick and has many cross bridges on it. The head of the cross bridge has two parts due to two heavy chains. There is a head and neck and tail region of the filament. There are two heavy chains and two pairs of light chains. The actin and ATP binding sites are on the heavy chains, but the light chains modulate the activity thereafter.

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16
Q

What are protein isoforms?

A

It’s the same protein with a similar function, but with a slightly different amino acid sequence

17
Q

Know all the parts of the sarcomere, all the different bands, which ones move and which ones don’t

A

You got it. Here I come youtube.

18
Q

What is a nebulin?

A

It is a thin filament protein- possibly a molecular ruler to determine thin filament length

19
Q

What is excitation-contraction coupling?

A

It is the mechanism by which an AP in the sarcolemma initiates muscle contraction- it is a rapid and very large increase in the free Ca++ concentration

20
Q

T/F- When there is high enough cytosolic calcium, it can bind to the troponin complex which allows for cross bridge binding to actin and force is generated.

A

True

21
Q

The ATP concentration inside muscle cells is buffered by what?

A

Phosphocreatine (PCr) and creatine kinase

22
Q

Creatine kinase is found in high concentrations where on the sarcomere?

A

Right on the M line

23
Q

What are three sources of ATP production?

A

Creatine phosphate
Glycolysis
Oxidative phosphorylation

24
Q

T/F ATP is consumed during both contraction and relaxation?

A

True!