Mitochondrial DNA alterations in blood of the humans exposed to N, N-dimethylformamide

• Published in: Chemico-biological interactions Vol. 165; no. 3; pp. 211 - 219
• Main Authors: Shieh, Dar-Bin, Chen, Chia-Chun, Shih, Tung-Sheng, Tai, Huo-Mu, Wei, Yau-Hui, Chang, Ho-Yuan
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier Ireland Ltd 20.02.2007
• Subjects: Acetylcysteine - analogs & derivatives; Acetylcysteine - urine; Adult; Biomarker; Biomarkers; Dimethylformamide; DNA Damage - drug effects; DNA, Mitochondrial - blood; DNA, Mitochondrial - chemistry; Formamides - metabolism; Formamides - toxicity; Humans; Male; Mitochondrial DNA common deletion; mtDNA copy number; N, N-Dimethylformamide; Occupational Exposure; N, N-Dimethylformamide; Biomarker; mtDNA copy number; Mitochondrial DNA common deletion
• ISSN: 0009-2797; 1872-7786
• DOI: 10.1016/j.cbi.2006.12.008

N, N-Dimethylformamide (DMF) has been widely used in industries because of its extensive miscibility with water and solvents. Its health effects include hepatotoxicity and male reproductoxicity, possibly linked with mitochondrial DNA (mtDNA) alterations including mtDNA common deletion (ΔmtDNA 4977) and mtDNA copy number. The relationship between DMF exposure and mtDNA alterations, however, has not been postulated yet. The purposes of this study were to investigate whether the DMF exposure is associated with ΔmtDNA 4977 and mtDNA copy number and to evaluate the DMF-derived mtDNA alterations are more associated with exposure to the airborne DMF concentrations or to the levels of two urinary DMF biomarkers of N-methylformamide (NMF) and N-acetyl- S-( N-methylcarbamoryl) cysteine(AMCC). Thirteen DMF-exposed workers and 13 age and seniority-matched control workers in a synthetic leather factory were monitored on their airborne DMF, NMF and AMCC in the urine as well as ΔmtDNA 4977 and mtDNA copy number in blood cells. We found that the frequencies of relative ΔmtDNA 4977 in DMF-exposed group were significantly higher than those in the control group. Moreover, elevation in the proportion of ΔmtDNA 4977 of individuals with high urine AMCC (U-AMCC) and airborne DMF levels were significantly higher than those without. We conclude that long-term exposure to DMF is highly associated with the alterations of mtDNA in urine and blood cells. The ΔmtDNA 4977 was more significantly related to repeated exposure to DMF and mtDNA copy number was more closely related to short-term DMF exposure. We also confirmed that U-AMCC is more appropriate to serve as a toxicity biomarker for DMF exposure than U-NMF. Further study with a larger number of subjects is warranted.