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Physical exercise increases urinary excretion of lipoxin A4 and related compounds
1 Department of Human Pathology, and 5 Experimental and Clinical Department of Medicine and Pharmacology, University of Messina, 98125 Messina; 2 Center of Excellence on Aging, and Departments of 3 Biomedical Science and 4 Medicine and Aging, University "G. D'Annunzio," 66013 Chi...
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Published in: | Journal of applied physiology (1985) 2003-06, Vol.94 (6), p.2237-2240 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | 1 Department of Human Pathology, and
5 Experimental and Clinical Department of Medicine and
Pharmacology, University of Messina, 98125 Messina;
2 Center of Excellence on Aging, and Departments of
3 Biomedical Science and 4 Medicine and
Aging, University "G. D'Annunzio," 66013 Chieti,
Italy
Lipoxins (LX) are
lipoxygenase-derived eicosanoids with potent anti-inflammatory
activities and vascular bed-dependent vasodilatory actions. LX can be
formed in vitro and in vivo in a number of conditions, and we have
reported that immunoreactive LXA 4 (iLXA 4 ) is
physiologically excreted with human urine. Using a recently developed
LX extraction method coupled to an ELISA, we examined whether
iLXA 4 excretion was modified by strenuous exercise, which is known to trigger potential LX-forming events. Maximal exertion significantly increased iLXA 4 urinary excretion in nine
healthy volunteers (0.061 ± 0.023 vs. 0.113 ± 0.057 ng/mg
creatinine; P = 0.028). iLXA 4 levels
returned to baseline after 6 h and increased, although at a
smaller extent, after 24 h. A significant correlation ( r = 0.988) was denoted between iLXA 4 ELISA
measurements and reversed-phase high-performance liquid chromatography
quantitation of a previously described urinary tetraene, confirming its
LXA 4 -related nature. These findings show for the first time
that an increase in excretion of LXA 4 -related compounds can
be observed in response to strenuous exercise. This may be the
reflection of an enhanced LX biosynthesis, which may represent a
safeguard mechanism that keeps the inflammatory reaction triggered by
physical stress under control.
arachidonic acid; lipoxygenase; inflammation; metabolism |
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ISSN: | 8750-7587 1522-1601 |
DOI: | 10.1152/japplphysiol.01004.2002 |