Somatic nervous system and muscle contraction Flashcards

1
Q

Cardiac muscles

A
  • Striated
  • Lines walls of the heart
  • Under involuntary control
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2
Q

Smooth muscle

A
  • Lines the visceral organs
  • Have a spiral like structure
  • Under involuntary control
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3
Q

Skeletal muscle

A
  • Allows us to move
  • Striated
  • Under voluntary control
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4
Q

How many muscle fibres are present in fasciculi?

A

Consist of 150 muscle fibres in bundles known as fasciculi

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5
Q

What is sarcolemma?

A

Muscle fibre membrane

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6
Q

What are present within the sarcoplasm?

A
  • Glycogen
  • Fat
  • Enzymes
  • Mitochondria
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7
Q

What is the sarcoplasmic reticulum?

A

SR is where Ca2+ is stored and released from

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8
Q

What are the thick filaments known as?

A

Known as myosin

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9
Q

What are the thin filaments known as?

A

Known as actin

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10
Q

Steps involved in calcium stimulated muscle contraction

A
  1. Myosin head hydrolyses ATP into ADP and inorganic phosphate. The energy released
  2. Ca2+ binds to troponin, which causes the tropomyosin to shift and exposes the myosin head binding site
  3. Myosin head binds into the myosin head binding site forming a cross bridge
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11
Q

What is required in order to break actin-myosin bonds?

A

ATP is required to break actin-myosin bonds

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12
Q

What does the somatic nervous system provide?

A

Provides voluntary control over skeletal muscle

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13
Q

What are efferent neurons?

A

Efferent neurons are that which innervate muscle i.e motor neurons

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14
Q

What is a motor unit?

A

A motor unit is a single motor neuron and all the muscle fibres it controls

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15
Q

What do single fibres do?

A

They contract completely or not at all

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16
Q

How can motor units regulate strength of muscle contraction?

A

Can regulate strength of muscle contraction by varying how many activated motor units there are

17
Q

Action potentials along neuromuscular junctions

A
  1. Action potential arrives along motor neuron
  2. This causes depolarisation and moves along the membrane and move down T-tubules which enter the muscle
  3. This causes depolarisation of the sarcoplasmic reticulum and this causes Ca2+ to be released
  4. The Ca2+ is released to the cytosol and causes contraction of the muscle
18
Q

What are the 2 types of cholinergic receptors?

A
  • Muscarinic(Primarily in CNS, GCPR and are slow)

- Nicotinic(In neurons/NMJs, and are fast)

19
Q

What happens when Ach binds to a nAchR?

A
  • 2 molecules of Ach bind to nicotinic AchR causing a conformational change
    • Opens ion pore
  • Opening of ion pore results in rapid increase in Na+/Ca2+ and membrane depolarisation leading to muscle contraction
20
Q

What is a tetanus contraction?

A

Its when the rate of action potential is so high that muscle doesn’t release between stimuli.

21
Q

Why does duchenne muscular dystrophy occur?

A

Occurs due to mutated gene dystrophin

22
Q

What does dystrophin do?

A

Dystrophin connects actin filaments to the sarcolemma, required for mechanical stability

23
Q

What does a lack of dystrophin do and what does this cause?

A

Lack of dystrophin causes dysfunction of sarcolemma stretch
-This causes ion pores to open and there’s increased
intracellular Ca2+

24
Q

What happens in Duchenne muscular dystrophy?

A

Degradation of structural proteins and CK is lost from cell into blood. CK is required for ATP

25
Q

What is ALS?

A

Its a neuron disease affecting motor neurons

26
Q

What is myasthenia gravis?

A

Chronic autoimmune NMD

27
Q

What does myasthenia gravis cause?

A

Causes skeletal muscle weakness and fatigue

28
Q

What happens in myasthenia gravis?

A
  • Body makes antibodies against AchR’s at NMJ’s

- Blocks AchR’s, increasing AchR degradation and causes impaired signal transduction

29
Q

What treatment is there for myasthenia gravis?

A

Treatment with acetyl cholinesterase inhibitors or immunosuppressants