ORIGINAL PAPER
Metabolism and in vitro assessment of the mutagenic activity of urinary extracts from rats after inhalation exposure to 1-methylnaphthalene
More details
Hide details
1
Nofer Institute of Occupational Medicine, Łódź, Poland
(Department of Translational Research)
2
QSAR Lab, Ltd, Gdańsk, Poland
3
Nofer Institute of Occupational Medicine, Łódź, Poland
(Department of Biological and Environmental Monitoring)
Online publication date: 2022-09-27
Corresponding author
Radosław Świercz
Nofer Institute of Occupational Medicine, Department of Translational Research, św. Teresy 8, 91-348 Łódź, Poland
Int J Occup Med Environ Health. 2022;35(6):731-46
KEYWORDS
TOPICS
ABSTRACT
Objectives: 1-Methylnaphthalene (1-MN) is composed of 2 benzene rings and belongs to polycyclic aromatic hydrocarbons. The metabolism of
1-MN in laboratory animals and bacteria leads to the formation of 1-naphthoic acid (1-NA). Material and Methods: In this study the distribution of 1-NA in lung, liver, spleen, kidney and urinary excretion of 1-NA in rats after single and repeated inhalation exposure to 1-MN vapors were investigated.
The activity of alanine aminotransferase (ALT), aspartate aminotransferase (AST) and cytochrome were measured of the rats. Genotoxic
effects were evaluated with the in vitro micronucleus test on V79 hamster fibroblasts. Results: The concentrations of 1-NA in the tissues of rats after
single and repeated exposure to 1-MN were dependent on the exposure dose. High levels of 1-NA were found in kidneys of animals after the single
and repeated exposure to 1-MN. With an increase of 1-MN dose, an increase in the activity of cytochrome P450 (CYP1A1 and CYP1A2) was observed
in the liver of rats. Compared to control animals, significantly higher ALT activity was noted in serum of rats exposed to 1-MN. The micronuclei
frequency in V79 cells exposed to 1-MN (in the range of analyzable concentrations; i.e., 5–25 μg/ml) did not differ significantly from the vehicle
control, whereas urine extracts from rats exposed to 1-MN induced a significant increase in the frequency of micronuclei compared to urine extracts
from the group of control animals. Conclusions: Metabolism of 1-MN in rats after the inhalation exposure leading to 1-NA was mainly observed
during the first day after the end of exposure. It is likely that 1-MN metabolites present in rat urine can induce the increased micronuclei frequency
as was shown in V79 cells. Int J Occup Med Environ Health. 2022;35(6):731–46