Abstract

Air pollution is a major risk for human health. Acetaldehyde is an environmental pollutant present in tobacco smoke, vehicle exhaust and several food products. Formation of DNA adducts has been regarded as a critical factor in the mechanisms of acetaldehyde mutagenicity and carcinogenesis. Acetaldehyde reacts with 2’-deoxyguanosine in DNA to primarily form N2-ethylidene-2'-deoxyguanosine (N2-ethylidene-dGuo). The subsequent reaction of N2-ethylidene-dGuo with another molecule of acetaldehyde gives rise to 1,N2-propano-2´-deoxyguanosine (1,N2-propanodGuo). In this study, on-line reverse-phase high-performance liquid chromatography (HPLC) separation with tandem mass spectrometry detection was utilized for the accurate quantification of 1,N2-propanodGuo and 1,N2-etheno-2'-deoxyguanosine (1,N2-edGuo) in tissues of rats exposed to 12 ppb, 33 ppb and 96 ppb acetaldehyde in atmospheric air for 50 days. A significant increase in the levels of 1,N2-propanodGuo was observed in lung tissues of rats exposed to 12 ppb (7.8/108 dGuo); 33 ppb (8.9/108 dGuo) and 96 ppb (11.6/108 dGuo) compared to controls (4.2/108 dGuo). For comparative purposes, the levels of 1,N2-etheno-2'-deoxyguanosine (1,N2-edGuo), which is produced from a,b-unsaturated aldehydes formed during the lipid peroxidation process were also measured. Elevated levels of 1,N2-edGuo were observed only in lung tissues of animals exposed to 96 ppb acetaldehyde. 1,N2-propanodGuo also differed quantitatively in liver but not in brain. The monitoring of 1,N2-propanodGuo levels in tissues provides important information on acetaldehyde genotoxicity and may contribute to the elucidation of the mechanisms associated with acetaldehyde exposure and cancer risk.Supported byFAPESP:2011/10048-5, CAPES, INCT Redoxoma:573530/2008-4,NAP Redoxoma: 2011.1.9352.1.8, CEPID Redoxoma:2013/07937-8.

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