Fast and Slow Muscle Flashcards

(36 cards)

1
Q

small motor units

A

less than 10 muscle fibres

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2
Q

large motor units

A

more than 100 muscle fibres

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3
Q

The force of muscle contraction is increased mainly by two

means:

A

• By activating more motor units i.e. recruitment
• By activating motor units more i.e. by increasing stimulus
frequency to cause summation or tetanus of individual motor
units

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4
Q

electromyography -EMG

A

The electrical activity of skeletal muscle can be recorded (electromyogram or EMG) using electrodes in or near the muscle

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5
Q

When will a clinician order an EMG

A

if a patient has signs or symptoms that may indicate a nerve or muscle disorder.

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6
Q

importance of EMG

A

often necessary to help diagnose or rule out a number of conditions such as:

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7
Q

myasthenia gravis

A

Diseases affecting the connection between the nerve and the muscle,

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8
Q

examples of disorders that affect motor units in brain or spinal cord

A

amyotrophic lateral sclerosis or polio

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9
Q

what are slow muscles adapted for

A

slow, sustained, tonic,

fatigue-resistant contractions e.g. postural muscles

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10
Q

fast muscles are adapted for

A

rapid, intense, phasic,

easily fatigued contractions e.g. gastrocnemius

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11
Q

muscle fibres are characterised based on

A

speed of contraction and ATP production

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12
Q

3 types of muscle fibres

A

– Type I: Slow-oxidative (small diameter)
– Type IIa: Fast-oxidative (intermediate diameter)
– Type IIb: Fast-glycolytic (large diameter)

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13
Q

fast muscle ATP production

A

= higher Myosin ATPase activity

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14
Q

oxidative

A

ATP produced by oxidative phosphorylation (Red Fibres)

– Much more efficient than glycolysis – more resistant to fatigue

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15
Q

glycolytic

A

generate ATP via anaerobic glycolysis (White Fibres)

– Inefficient method which also produces lactic acid

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16
Q

fast twitch speed

17
Q

slow twitch speed

18
Q

difference between cells and muscles

A

individual cells are either fast or slow
whole muscles have fast AND slow cells
whole muscle is seen as fast or slow depending on the majority of fast or slow cells

19
Q

size of motor neurons in slow fibres in comparison to fast fibres

A

motor neurons in slow fibres are smaller than fast fibres

20
Q

when will small cell bodies be recruited

A

Their cell bodies are more excitable and are the first

to be recruited during moderate contractions.

21
Q

when will fast cell bodies be recruited

A

during more intense contractions

22
Q

does training have an effect on fast and slow fibre numbers

A

Training has little effect on fast and slow fibre numbers
• Training regimens cannot alter fiber type or the
expression of myosin isoforms.
• Elite sprinters have high numbers of fast fibres

23
Q

training can

A

Improve oxidative capacity (more resistant to fatigue)
• Increase blood supply/number of mitochondria
– Change muscle fibre diameter - hypertrophy - in short high intensity anaerobic exercise

24
Q

atrophy

A

Muscle decreases in mass if not routinely used

25
lesion of motor nerves in skeletal muscle causes
A lesion of the motor nerves to skeletal muscle (lower motor neuron lesion) causes flaccid paralysis
26
Fasciculations
Visible twitching caused by release of Ach from | degenerating motoneurons
27
where does Type I and type II atrophy occur
peripheral neuropathies, disuse (bedrest, | spaceflight, immobilization), myasthenia gravis etc
28
where does type II atrophy mainly occur
with Duchenne muscular dystrophy and ageing | sarcopaenia
29
Type II hypertrophy occurs
with weight training
30
psuedohypertrophy
in calf muscles in Duchenne muscular dystrophy ("false | enlargement," because the muscle tissue is abnormal.)
31
neuropathy
(disease affecting nerves) in the central or | peripheral nervous system or both (peripheral nerves,
32
example of neuropathy
multiple sclerosis
33
junctionopathy
disease affecting (Neuromuscular junctions,
34
example of junctionopathy
myasthenia gravis
35
myopathy
(disease affecting muscle,
36
examples of myopathy
muscular | dystrophies