fast and slow muscles & muscle disorders Flashcards

1
Q

what is a motor unit?

A

consists of a motor neuron and all of the muscle fibres that it innervates

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2
Q

what kind of muscles have large vs small motor units?

A
  • postural muscles - large MU
  • muscles requiring precise control - extraocular and hand muscles
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3
Q

by what 2 ways can the force of muscle contraction be increased?

A
  1. recruitment - activating more MU’s
  2. increasing stimulus freq to cause summation or tetanus
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4
Q

how can the electrical activity be recorded on skeletal muscle?

A

by electromyography

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5
Q

what kind of muscle disorder and pathologies can be diagnosed or ruled out by an electromyography?

A
  • muscular dystrophy - muscle disorder - hereditary condition
  • myasthenia gravis - autoimmune disorder - decreasing no of Ach receptors
  • amyotrophic lateral sclerosis/ motor neuron disease
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6
Q

why would a clinician order an electromyography?

A

to detect a nerve or muscle disorder

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7
Q

what are slow muscles adapted for?

A

slow sustained and fatigue resistant contractions
eg postural muscles

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8
Q

what are fast muscles adapted for?

A
  • rapid, intense and easily fatigued contractions
  • eg gastrocnemius muscle
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9
Q

what 2 things are the 3 types of muscle fibres characterised on?

A
  • speed of contraction
  • ATP production
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10
Q

what are the 3 types of muscle fibres?

A
  • Type I - slow oxidative
  • Type IIA- fast oxidative
  • Fast IIb- fast - glycolytic
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11
Q

do the fast or slow muscle fibres have a higher myosin ATPase?

A
  • fast muscle fibres
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12
Q

by what method do type iib fibres generate atp?

A

by anaerobic glycolysis

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13
Q

why are slow muscles red?

A
  • mitochondria
  • myoglobin
  • high level of vascularity
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14
Q

why are fast muscles white?

A

due to lack of mitochondria, myoglobin and vascularity

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15
Q

what is the function of myosin ATPase?

A
  • catalyses the reaction that breaks down ATP into ADP and phosphate
  • ie ATP hydrolysis
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16
Q

do whole muscles consist of both fast and slow muscle fibres?

A

yes they consist of both slow oxidative and fast oxidative and glycolytic fibres

17
Q

what type of muscle fibres are usually recruited first?

A

slow oxidative fibres

18
Q

what can training change in a muscle fiber?

A
  • can imporve oxidative capacity - ie increase number of mitochondria
  • change muscle diameter - ie hypertrophy or increase in muscle size
19
Q

what is atrophy?

A

decrease in muscle mass / muscle wasting

20
Q

what can happen as a result of a lower motor neuron lesion (lesion in peripheral nerve)?

A
  • flaccid paralysis
  • hyporeflexia
  • atrophy
21
Q

what is flaccid paralysis?

A
  • neurological condition characterised by weakness or paralysis and reduced muscle tone
  • may be caused by disease or trauma affecting the nerves
22
Q

what is muscle fasciculation characterised by?

A
  • visible twitching caused by release of ACH from degenerating motorneurons
23
Q

what can a failure to regenerate the nerves result in?

A

type 1 and 11 fibre atrophy

24
Q

what conditions and situations lead to type I and II atrophy?

A
  • peripheral neuropathies
  • disuse - eg bedrest, immobilisation
  • myasthenia gravis
  • muscular dystrophy
  • ageing - sarcopenia - age related loss of muscle
25
Q

what is a junctionopathy?

A

pathology affecting the NMJ eg myasthenia gravis

26
Q

what is myopathy?

A

disease affecting the muscle eg muscular dystrophies