Edrissi Bahar, Taghizadeh Koli, Moeller Benjamin C, Yu Rui, Kracko Dean, Doyle-Eisele Melanie, Swenberg James A, Dedon Peter C
Department of Environmental Sciences and Engineering, University of North Carolina , Chapel Hill, North Carolina 27514, United States.
Lovelace Respiratory Research Institute , Albuquerque, New Mexico 87108, United States.
Chem Res Toxicol. 2017 Aug 21;30(8):1572-1576. doi: 10.1021/acs.chemrestox.7b00075. Epub 2017 Jul 27.
Exposure to both endogenous and exogenous formaldehyde has been established to be carcinogenic, likely by virtue of forming nucleic acid and proteins adducts such as N-formyllysine. To better assess N-formyllysine as a biomarker of formaldehyde exposure, we studied accumulation of N-formyllysine adducts in tissues of rats exposed by inhalation to 2 ppm [CH]-formaldehyde for 7, 14, 21, and 28 days (6 h/day) and investigated adduct loss over a 7-day postexposure period using liquid chromatography-coupled tandem mass spectrometry. Our results showed formation of exogenous adducts in nasal epithelium and to some extent in trachea but not in distant tissues of lung, bone marrow, or white blood cells, with a 2-fold increase over endogenous N-formyllysine over a 3-week exposure period. Postexposure analyses indicated a biexponential decay of N-formyllysine in proteins extracted from different cellular compartments, with half-lives of ∼25 and ∼182 h for the fast and slow phases, respectively, in cytoplasmic proteins. These results parallel the behavior of DNA adducts and DNA-protein cross-links, with protein adducts cleared faster than DNA-protein cross-links, and point to the potential utility of N-formyllysine protein adducts as biomarkers of formaldehyde.
内源性和外源性甲醛暴露均已被证实具有致癌性,可能是通过形成核酸和蛋白质加合物,如N-甲酰赖氨酸。为了更好地评估N-甲酰赖氨酸作为甲醛暴露的生物标志物,我们研究了吸入2 ppm [CH]-甲醛(每天6小时)7、14、21和28天的大鼠组织中N-甲酰赖氨酸加合物的积累情况,并使用液相色谱-串联质谱法研究了暴露后7天内加合物的损失情况。我们的结果表明,外源性加合物在鼻上皮中形成,在气管中也有一定程度的形成,但在肺、骨髓或白细胞的远处组织中未形成,在3周的暴露期内,外源性加合物比内源性N-甲酰赖氨酸增加了2倍。暴露后分析表明,从不同细胞区室提取的蛋白质中,N-甲酰赖氨酸呈双指数衰减,在细胞质蛋白质中,快速和慢速阶段的半衰期分别约为25小时和182小时。这些结果与DNA加合物和DNA-蛋白质交联的行为相似,蛋白质加合物的清除速度比DNA-蛋白质交联快,表明N-甲酰赖氨酸蛋白质加合物作为甲醛生物标志物具有潜在的实用性。