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Erythropoiesis and Performance after Two Weeks of Living High and Training Low in Well Trained Triathletes
Abstract The purpose of our study was to evaluate hematologic acclimatization during 2 weeks of intensive normoxic training with regeneration at moderate altitude (living high-training low, LHTL) and its effects on sea-level performance in well trained athletes compared to another group of equally t...
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Published in: | International journal of sports medicine 2002-11, Vol.23 (8), p.561-566 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Abstract
The purpose of our study was to evaluate hematologic acclimatization
during 2 weeks of intensive normoxic training with regeneration at moderate
altitude (living high-training low, LHTL) and its effects on sea-level
performance in well trained athletes compared to another group of equally
trained athletes under control conditions (living low - training low,
CONTROL). Twenty-one triathletes were ascribed either to LHTL
(n = 11; age: 23.0 ± 4.3 yrs;
V˙O
2
max: 62.5 ± 9.7
[ml × min
-1
× kg
-1
])
living at 1956 m of altitude or to CONTROL (n = 10;
age: 18.7 ± 5.6 yrs; V˙O
2
max:
60.5 ± 6.7 ml × min
-1
× kg
-1
)
living at 800 m. Both groups perfomed an equal training schedule at
800 m. V˙O
2
max, endurance performance, erythropoietin in
serum, hemoglobin mass (Hb
tot
, CO-rebreathing method) and
hematological quantities were measured. A tendency to improved performance in
LHTL after the camp was not significant (p < 0.07).
Erythropoietin concentration increased temporarily in LHTL
(Δ 14.3 ± 8.7 mU × ml
-1
;
p < 0.012). Hb
tot
remained unchanged in LHTL
whereas was slightly decreased from 12.5 ± 1.3 to
11.9 ± 1.3g × kg
-1
in
CONTROL (p < 0.01). As the reticulocyte number tended to
higher values in LHTL than in CONTROL, it seems that a moderate stimulation of
erythropoiesis during regeneration at altitude served as a compensation for an
exercise-induced destruction of red cells. |
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ISSN: | 0172-4622 1439-3964 |
DOI: | 10.1055/s-2002-35533 |