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. Author manuscript; available in PMC: 2016 Apr 1.
Published in final edited form as: Toxicol Lett. 2014 Aug 2;230(1):57–61. doi: 10.1016/j.toxlet.2014.07.029

TABLE 1.

Direct assay measurement of substrate hydrolysis by human serum PON1. Activities are expressed as micromoles of substrate hydrolyzed per minute per liter of serum, means ± SD, n=10. [Data on paraoxon and diazoxon were calculated for this subset of subjects only, but were collected for and methods were described in the Coombes et al. (2011) study.] Values within a substrate with the same superscript letter are not statistically different (p≤0.05).

Substrate High RR Low RR High QQ Low QQ
Chlorpyrifos-oxon 11,023 ± 722A 9,467 ± 798B 8,809 ± 672B 6,030 ± 1015C
Paraoxon 720 ± 40A 530 ± 53B 259 ± 53C 139 ± 21D
Diazoxon 9,255 ± 1,040A 5,699 ± 669B 13,250 ± 381C 6,892 ± 620D