Peripheral Fatigue Flashcards

1
Q

Physiological definition of fatigue

A

Failure to maintain the required or expected force or power

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2
Q

Definition of weakness

A

Failure to generate the required or expected force or power

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3
Q

Marks of fatigue

A

Can’t reach the same force level
Shape of tetanus curve changes - takes longer to reach the plateau and also takes longer for the muscle to relax

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4
Q

Excitation-contracting coupling

A

ATP dependent processes
Myosin head force development
3Na out, 2K in results in resting potential
Calcium pump

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5
Q

Excitation-contraction coupling in fatigue/energy crisis

A

If there is little energy, these systems can be a source of fatigue because the pumps in these systems need ATP to work

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6
Q

Which type of muscle fibres are ‘unfatigueable’

A

Type II because they have mitochondria

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7
Q

What does caffeine do?

A

Facilitates the opening of ryanodine receptors in the sarcoplasmic reticulum

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8
Q

Inhibitory effects of calcium release

A

High AMP
High ADP
Very low ATP
Mg concentration doubles at fatigue because ADP, AMP and IMP have lower affinity for Mg than ATP

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9
Q

Calcium re-uptake

A

Evidence in amphibians (none in mammalian muscle) that calcium re-uptake is the cause for slower relaxation
The quicker the calcium is taken up, the quicker the muscle can relax

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10
Q

Potassium gradients during fatigue

A

Accumulation of K in extracellular space because T-tubular membrane has a large SA and the T-tubular network has a small volume.
More difficult to induce action potentials

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11
Q

Inorganic phosphate inducing fatigue

A

Phosphocreatine level go down (hydrolysed into inorganic phosphate and creatine).
Ph also drops a lot in fatigue which causes an increase in protons.
Inorganic phosphate bind to the calcium in the cell - calcium can’t help with muscle contraction = fatigue

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12
Q

ATP Depletion

A

Studies show that ATP in a cell does not drop below 60% f resting levels (whole muscle)
Isolation fibre: down to 20%
Localised ATP depletion possible in the space between T-tubule and sarcoplasmic reticulum (Triad junction)

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13
Q

What is compartmentalisation?

A

where metabolite vary within different compartments of the cell

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14
Q

What is compartmentalisation used to explain?

A

ADP tightly regulated and does not acculumate
ATP average levels do not fall enough to affect cross-bridge function
H+ plays a minor role in physiological condition (PH, temperature)

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15
Q

Metabolism for runners

A

The better trained you are, the better your fat metabolism
It is advantageous for a runner to have a higher metabolism because it slows down fatigue

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16
Q

Glycogen as a fuel

A

No fuel = no power
Glycogen is an essential substrate

17
Q

Glycogen depletion

A

During work, the muscle glycogen falls successively to values approaching 0, the working capacity decreases when the glycogen store is depleted

18
Q

CHO Feeding

A

Maintains CHO oxidation - little glycogen used from muscle
Doesn’t prevent exhaustion, it just takes longer to take place

19
Q

Restoring glucose after fatigue

A

Force and calcium drop at some point in the repetitive movement
When glucose has been restored (feeding) after fatigue, calcium levels increase again

20
Q

Not restoring glucose after fatigue

A

If you don’t feed, calcium levels don’t recover and the second set of activity is much shorter = short time to exhaustion