EPO Flashcards

1
Q

What is EPO?

A
  • Erythropoietin - produced in the kidneys to stimulate RBC production
  • EPO injection elevate Hb and Hct
  • Hypoxic conditions creates EPO - produced during big bleed as loss of RBC creates hypoxic conditions
  • We can artificially administer EPO
  • Traditionally, athletes will take blood and freeze it, liver detects drop in RBC and therefore creates more EPO. Infuse the blood back into the body and there is extra EPO
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2
Q

EPO in the muscle tissue:

Vitro
Rodent
Human

A

Vitro
- EPO improves JAK2, AKT, STATS (signalling proteins)

Rodent
- Unsure about JAK2, improves AKT, doesn’t improve STATS

Human
- JAK2 not studied, doesn’t improve AKT or STATS

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3
Q

Birkland et al (2000)

A
  • Injected EPO for 30 days, 3x per week vs control

Haematocrit:

  • Rise in Hct to 50% (International Cycling Union Upper Limit)
  • 2 subjects stopped as Hct level got too high
  • RBC has short half lift, returned to baseline when injections stopped

Haemoglobin
- Increased to about 10%

  • Increased Vo2max and TTE with EPO - falls back to baselines after administration
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4
Q

Thomson et al (2007)

A
  • Injections aimed to peak Hct levels at 50%
  • Less injections over longer duration (harder to detect)
  • Increased level of arterial levels of oxygen
  • Sig increase in Watt max vs CON at 4 and 11 weeks
  • Vo2max sig increased at 4 and 11 weeks
  • Increased TTE at same absolute but not relative intensity in week 11 compared to week 1
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5
Q

Durussell et al (2013)

A

Runners vs non-runners - EPO administered for 4 weeks

Vo2max:
- Increased in runners and non-runners after 4 weeks

  • Increased in non-runners but not runners after 8 weeks

TT - 3k:

  • 6% improvement after 4 weeks
  • 3% improvement after 8 weeks
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6
Q

Ekholm et al (1991)

A
  • Increased max aerobic power when taking EPO

- Max aerobic power returned to baseline after 4-weeks of administration

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7
Q

Nordsborg et al (2014)

A
  • Injection given every other day for 2 weeks, followed by 1 week for the remainder of the trial
  • Measured pre/post 15min steady state before ramp test to exhaustion
  • Post group had 2 hour break before haemodilation
  • No difference in potassium and hydrogen ion accumulation pre/post
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8
Q

Guadalupe-Gau et al (2015)

A
  • 6 males given EPO to get to 50% Hct

- EPO increase mitochondrial fat oxidation (9%) but not systemic fat oxidation

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9
Q

Wilkerson et al (2015)

A
  • 15 subjects, EPO and CON, weekly injections for 4 weeks
  • No difference in oxygen uptake kinetics with/without EPO
  • EPO group increase TTE and intensity of exercise nut not oxygen uptake kinetics
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10
Q

Health risks of EPO

A
  • Increased risk of blood clotting
  • Elevations in systolic blood pressure
  • Compromised thermoregulatory system
  • Dehydration
  • Fall in iron indicated by fall in ferritin (Birkland et al, 2000)
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