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1 Department of Internal Medicine VII/Sportsmedicine, University Hospital, 69115 Heidelberg; 2 Section of Vascular Medicine, Department of Medicine IV, University Hospital, 72076 Tübingen, Germany; 3 Department of Anatomy and Cell Biology III, University of Heidelberg, 69120 Heidelberg; 4 Division of Immunochemistry, German Cancer Research Institute, 69120 Heidelberg; and 5 Department of Pathology, Technical University of Dresden, 01307 Dresden, Germany
In healthy individuals, prolonged intensive
physical exercise leads to an activation of blood coagulation that
results in the formation of thrombin and fibrin. This study
investigated whether oxidative stress during intensive physical
exercise induces tissue factor (TF) via activation of the
redox-responsive transcription factor nuclear factor-
B (NF-
B).
Twelve young men performed a standardized 1-h maximal run on a
treadmill that gave rise to significant increases of markers of
thrombin and fibrin formation. The ratio of intracellular reduced to
oxidized glutathione as measured by HPLC decreased from 23.3 ± 10.7 to 14.2 ± 6.5 (P < 0.05), indicating the
generation of free radicals during exercise. Electrophoretic mobility
shift assays from nuclear extracts of peripheral blood
mononuclear cells revealed that exercise testing increased
NF-
B (p50/p65) binding activity to a NF-
B consensus sequence by
105 ± 68% (P < 0.01) but did not affect NF-
B
(p65/c-Rel) binding to a nonconsensus-
B-like site present in the TF
promoter. Consistently, there was no exercise-induced increase in TF
expression as demonstrated by TF-specific immunofluorescence staining
and ELISA. Thus selective activation of NF-
B (p50/p65) during
intensive physical exercise does not result in the expression of TF,
suggesting that the TF-dependent pathway in peripheral blood
mononuclear cells does not account for exercise-induced formation of
thrombin and fibrin.
nuclear factor-
B; glutathione; factor VII; hemostasis
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