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J Appl Physiol (February 14, 2003). doi:10.1152/japplphysiol.01004.2002
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Submitted on October 29, 2002
Accepted on January 30, 2003

Physical exercise increases urinary excretion of lipoxin A4 and related compounds

Sebastiano Gangemi1, Graziella Luciotti2, Etrusca D'Urbano3, Agostino Mallamace4, Domenico Santoro4, Guido Bellinghieri4, Giovanni Davi3, and Mario Romano2*

1 Department of Human pathology, University of Messina, Messina, Italy
2 Center of Excellence on Aging, University of Chieti, Chieti, Italy; Department of Biomedical Sciences, University of Chieti, Chieti, Italy
3 Center of Excellence on Aging, University of Chieti, Chieti, Italy; Department of Medicine and Aging, University of Chieti, Chieti, Italy
4 Experimental and Clinical Department of Medicine and Pharmacology, University of Messina, Messina, Italy

* To whom correspondence should be addressed. E-mail: mromano{at}unich.it.

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 (i)LXA4 is physiologically excreted with human urine. Using a recently developed LX extraction method coupled to an enzyme-linked immunosorbent assay (ELISA), we examined whether iLXA4 excretion was modified by strenuous exercise, which is known to trigger potential LX-forming events. Maximal exertion significantly increased iLXA4 urinary excretion in nine healthy volunteers (0.061 ± 0.023 versus 0.113 ± 0.057 ng/mg creatinine; P = 0.028). iLXA4 levels returned to baseline after 6 h to increase, although at a smaller extent, after 24 h. A significant correlation (r = 0.988) was denoted between iLXA4 ELISA measurements and RP-HPLC quantitation of a previously described urinary tetraene, confirming its LXA4-related nature. These findings show for the first time that an increase in excretion of LXA4-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 under control the inflammatory reaction triggered by physical stress.




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Proc. Natl. Acad. Sci. USAHome page
N. Chiang, E. A. Bermudez, P. M. Ridker, S. Hurwitz, and C. N. Serhan
Aspirin triggers antiinflammatory 15-epi-lipoxin A4 and inhibits thromboxane in a randomized human trial
PNAS, October 19, 2004; 101(42): 15178 - 15183.
[Abstract] [Full Text] [PDF]




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