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Investigation of the cumulative tissue doses of naphthoquinones in human serum using protein adducts as biomarker of exposure
Authors:Po-Hsiung Lin  Dar-Ren Chen  Chia-Hua Lin
Affiliation:a Department of Environmental Engineering, National Chung Hsing University, Taichung 402, Taiwan
b Comprehensive Breast Cancer Center, Changhua Christian Hospital, Changhua, Taiwan
Abstract:
Both 1,2-naphthoquinone (1,2-NPQ) and 1,4-naphthoquinone (1,4-NPQ) are reactive metabolites of naphthalene that are thought to be responsible for the naphthalene-induced cytotoxicity and genotoxicity. The aim of this study was to investigate the cumulative tissue dose of 1,2-NPQ and 1,4-NPQ in human serum derived from blood donors in Taiwan via measurements of albumin adducts by a methodology, which employs trifluoroacetic acid anhydride and methanesulfonic acid to selectively cleave cysteinyl adducts on proteins. Both 1,2-NPQ and 1,4-NPQ adducts were detected in all male and female subjects (n = 22). The median levels of 1,2-NPQ adduct in human subjects were estimated to be 268 (range 139-857) and 203 (range 128-1352) (pmol/g) in male (n = 11) and female (n = 11) subjects, respectively. In contrast, the median levels of 1,4-NPQ adduct were estimated to be 45.0 (range 22.0-117) and 38.9 (range 21.5-172) (pmol/g) in male and female subjects, respectively. We noticed that levels of 1,2-NPQ adduct were significantly correlated with those of 1,4-NPQ adduct (correlation coefficient r = 0.643, p < 0.01). Results from in vitro experiments confirmed that the production of naphthoquinones-derived adducts on serum albumin increased with increased concentration of naphthoquinones (0-100 μM). Linear relationships were observed over the range of concentration. Time-course experiments suggested that both 1,2-NPQ and 1,4-NPQ-derived adducts rapidly reached maximum values at 10 min mark and remained constant thereafter. The reaction rate constant analyses indicated that the second-order rate constants, representing in vitro reactions between naphthoquinones and cysteine residues of serum albumin, were estimated to be 0.0044/0.0002 L(g protein)−1 h−1, respectively. Overall, the cumulative tissue doses of 1,4-NPQ (217-316 nM h) in male and female subjects were ∼3-fold greater than those of 1,2-NPQ (76-98 nM h) in the study population. The initial concentrations of serum 1,2-NPQ and 1,4-NPQ in the study population were estimated to be between 145-188 and 807-1175 nM, respectively. We conclude that the relatively large amounts of naphthoquinones present in human serum may point to toxicological consequences.
Keywords:1,2-NPQ, 1,2-naphthoquinone   1,2-NPQ-Alb and 1,4-NPQ-Alb, adducts resulting from reaction of 1,2- and 1,4-NPQ with cysteinyl residues in Alb   1,2-NPQ-NAC and 1,4-NPQ-NAC, reaction products of 1,2- and 1,4-NPQ with N-acetyl-l-cysteine   1,2-NPQ-S-TFA, trifluoroacetyl derivative of 1,2-NPQ adduct after the MT assay   1,4-NPQ, 1,4-naphthoquinone   1,4-NPQ-S-TFA, trifluoroacetyl derivatives of 1,4-NPQ adduct after the MT assay   Alb, albumin   EI, electron impact   GC-MS, gas chromatograph and mass spectrometer   GSH, glutathione   Hb, hemoglobin   HPLC, high performance liquid chromatography   MSA, methanesulfonic acid   MT assay, methanesulfonic acid and trifluoroacetic acid anhydride assay   NAC, N-acetyl-l-cysteine   NICI, negative ion chemical ionization   NPO1-Alb and NPO2-Alb, adducts resulting from reaction of NPO with cysteinyl residues in Alb   PAHs, polycyclic aromatic hydrocarbons   SD, standard deviation   TFA, trifluoroacetyl   TFAA, trifluoroacetic acid anhydride
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