UPTAKE AND METABOLISM OF CARCINOGENIC LEVELS OF TOBACCO-SPECIFIC NITROSAMINES BY SUDANESE SNUFF DIPPERS

Citation
Se. Murphy et al., UPTAKE AND METABOLISM OF CARCINOGENIC LEVELS OF TOBACCO-SPECIFIC NITROSAMINES BY SUDANESE SNUFF DIPPERS, Cancer epidemiology, biomarkers & prevention, 3(5), 1994, pp. 423-428
Citations number
33
Categorie Soggetti
Public, Environmental & Occupation Heath
ISSN journal
10559965
Volume
3
Issue
5
Year of publication
1994
Pages
423 - 428
Database
ISI
SICI code
1055-9965(1994)3:5<423:UAMOCL>2.0.ZU;2-R
Abstract
It was recently reported that toombak, a type of snuff used in the Sud an, contained unusually high levels of tobacco-specific nitrosamines. To estimate the internal dose of 4-(methylnitrosamino)-1-(3-pyridyl)-1 -butanone (NNK) received by individuals who use this type of tobacco, urine from a group of users was analyzed for 2 metabolites of NNK, 4-( methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) and its O-glucuronid e, NNAL-Gluc. NNK is a strong lung carcinogen believed to contribute t o human lung cancer. NNAL is also a lung carcinogen. NNAL and NNAL-Glu c were analyzed by gas chromatography with a nitrosamine selective det ector. The average levels detected were 0.39 +/- 0.14 (SD) nmol/ml uri ne (n = 7) and 0.88 +/- 0.50 nmol/ml urine (n = 7), respectively. In a 24-h period, these individuals would excrete from 0.12 to 0.44 mg of these two metabolites (expressed per mg NNAL). Therefore, assuming chr onic toombak use, the minimum daily dose of NNK to which these users w ere exposed was 0.12-0.44 mg. This is the highest documented uptake of a nonoccupational carcinogen. Two diastereomers of NNAL-Gluc were pre sent in all urine samples analyzed. Previously, these two diastereomer s were identified in the urine of an NNK-treated patas monkey but only one was detected in the urine of NNK-treated rats. The level of the 4 -hydroxy-1-(3-pyridyl)-1-butanone releasing hemoglobin adduct was also quantified in these individuals. This adduct is believed to be a meas ure of NNK activation. The levels ranged from 68 to 323 fmol/g hemoglo bin [mean, 148 +/- 104 (SD)]. The wide range of adduct levels which we re observed suggests that despite similar levels of NNK exposure, ther e are significant differences in the ability of individuals in this po pulation to activate NNK, as well as potential differences in their ca ncer risk.