Abstract
Isoprostane assays have significant potential for use as molecular biomarkers of human oxidant stress (Morrow et al. 1999, Lawson et al. 1999). Recent studies indicate that: (a) significant amounts of F2 isoprostanes derived from systemic oxidant stress are metabolized before excretion, (b) a significant quantity of free F2 isoprostanes are produced by the kidney, so free isoprostanes detected in urine may not accurately reflect systemic oxidant stress and (c) 2,3-dinor-5,6-dihydro-15-F2tIsoprostane (F2-IsoP-M, IsoP-M), a major urinary metabolite of systemic 8-iso-PG F2Œ, has recently been identified (Figure 1). Urinary F2-IsoP-M may, therefore, prove to be an excellent marker for systemic oxidant stress. Our goal is to develop a sensitive and specific immunoassay for F2-IsoP-M, which should provide a simple non-invasive method for routine quantitative assessment of human oxidant stress.
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