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. Author manuscript; available in PMC: 2016 Dec 20.
Published in final edited form as: Chem Res Toxicol. 2015 Dec 18;29(1):87–95. doi: 10.1021/acs.chemrestox.5b00425

Table 3.

O6-POB-dGuo levels in (A) esophageal mucosa and (B) oral mucosa. Adduct levels are expressed as mean ± standard deviation (fmol/mg DNA).

Dosagea (R)-NNN (S)-NNN Rac-NNN Additiveb Synergyc p-valued
A. Esophageal mucosa
Low 2.4 ±1.0 4.5 ±1.7 11.2 ±1.6 6.9 ±2.0 61% 0.004
Median 5.5 ±1.2 8.5 ±1.3 18.4 ±3.3 14.0 ±1.7 31% 0.041
High 14.7 ±3.3 16.7 ±4.9 26.4 ±10.8 31.5 ±5.9 −16% 0.469
B. Oral mucosa
Low 0.8 ±0.3 2.2 ±0.7 3.5 ±1.0 3.0 ±0.8 15% 0.525
Median 2.0 ±0.6 3.3 ±0.6 5.2 ±0.1 5.3 ±0.8 −1% 0.936
High 3.9 ±1.0 5.1 ±0.8 8.6 ±1.5 9.0 ±1.3 −4% 0.744
a

Low dosage level: 7 ppm (R)-NNN, 7 ppm (S)-NNN and 14 ppm Rac-NNN; Median dosage level: 14 ppm (R)-NNN, 14 ppm (S)-NNN and 28 ppm Rac-NNN; High dosage level: 28 ppm (R)-NNN, 28 ppm (S)-NNN and 56 ppm Rac-NNN.

b

The additive sum was calculated from the corresponding enantiomers.

c

Synergy was defined by the percentage difference between the racemic NNN group and the additive sum.

d

p-values were calculated for comparison of the adduct level from racemic NNN group and the additive sum of corresponding enantiomers at each dosage level. A p-value less than 0.05 was considered statistically significant.