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DNA Adduct Formation of the Food-Derived Mutagen 2-Amino-3-methylimidazo[4,5-f]quinoline in Nonhuman Primates Undergoing Carcinogen Bioassay

Authors :
Turesky, R. J.
Gremaud, E.
Markovic, J.
Snyderwine, E. G.
Source :
Chemical Research in Toxicology; February 29, 1996, Vol. 9 Issue: 2 p403-408, 6p
Publication Year :
1996

Abstract

DNA adduct formation of 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) was investigated in cynomolgus monkeys. The pattern and distribution of DNA adducts examined by <SUP>32</SUP>P-postlabeling were similar in all tissues 24 h after a single oral dose of IQ (20 mg/kg). The highest DNA adduct levels were found in the liver (3.67−11.19 adducts per 10<SUP>7</SUP> bases), followed by kidney (0.53−1.16 adducts per 10<SUP>7</SUP> bases), with comparable adduct levels detected in colon, heart, and pancreas (0.15−0.40 adducts per 10<SUP>7</SUP> bases). Two 2‘-deoxyguanosine (dG) adducts accounted for approximately 90% of the observed lesions in all tissues. N-(Deoxyguanosin-8-yl)-2-amino-3-methylimidazo[4,5-f]quinoline (dG-C8-IQ) was the major adduct and accounted for approximately 50−80% of the adducts, followed by 5-(deoxyguanosin-N<SUP>2</SUP>-yl)-amino-3-methylimidazo[4,5-f]quinoline (dG-N<SUP>2</SUP>-IQ) which accounted for 20−40% of the adducts. DNA adduct formation was also investigated in animals undergoing carcinogen bioassay with IQ administered at 10 or 20 mg/kg, 5 days per week for up to 9.2 years. In chronically treated animals, the DNA adduct levels in pancreas, kidney, and heart increased on average by 40- to 90-fold over those observed in animals given a single dose, while only 3- to 10-fold increases in adducts were observed in colon and liver. A sharp increase in the contribution of dG-N<SUP>2</SUP>-IQ to total DNA adducts occurred in all slowly dividing tissues during chronic treatment, and dG-N<SUP>2</SUP>-IQ became the predominant lesion. There was no preferential accumulation of dG-N<SUP>2</SUP>-IQ in the colon, a tissue with a high rate of cell division, and dG-C8-IQ remained the predominant lesion. These findings point to a preferential removal of the dG-C8-IQ adduct by enzyme repair system(s) in slowly dividing tissues. The respective roles of dG-N<SUP>2</SUP>-IQ and dG-C8-IQ, and the involvement of adduct repair in the potent hepatocarcinogenicity of IQ, merit further investigation.

Details

Language :
English
ISSN :
0893228X and 15205010
Volume :
9
Issue :
2
Database :
Supplemental Index
Journal :
Chemical Research in Toxicology
Publication Type :
Periodical
Accession number :
ejs1061031