Elevated plasma levels of F2(α) isoprostane in cystic fibrosis

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Abstract

Cystic fibrosis (CF) is associated with chronic lung infection, inflammation, and elevated indices of oxidative stress. Recently, isoprostanes were shown to be a reliable in vivo marker of oxidant injury with 8-iso-PGF2(α), shown to cause airflow obstruction and plasma exudation in guinea pig lung. The present study was designed to examine the relationship between 8-iso-PGF2(α) levels, plasma antioxidants, and clinical status in CF. We hypothesized that plasma 8-iso-PGF2(α) levels would be higher in subjects with CF compared to healthy controls. Plasma 8- iso-PGF2(α) levels were prospectively measured in 22 subjects with CF and nine healthy controls using an 8-isoprostane enzyme immunoassay kit along with plasma vitamins A, E, and β-carotene. Plasma 8-iso-PGF2(α) levels were shown to be significantly elevated in the CF subjects compared to controls (319.6 ± 52.6 vs. 145.0 ± 21.0 pg/mL, P = 0.005). Plasma levels of antioxidants were significantly lower for the CF subjects compared to the controls (vitamin A, P < 0.003; vitamin E, P < 0.001; and β-carotene, P < 0.01). This study confirms significantly elevated lipid peroxidation in CF using 8-iso-PGF2(α) levels.

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Collins, C. E., Quaggiotto, P., Wood, L., O’Loughlin, E. V., Henry, R. L., & Garg, M. L. (1999). Elevated plasma levels of F2(α) isoprostane in cystic fibrosis. Lipids, 34(6), 551–556. https://doi.org/10.1007/s11745-999-0397-1

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