Abstracts
Five nitro musk compounds are widely used as fragrance ingredients in perfumes, lotions and detergents; as food additives in cigarettes and fish baits, and in such technical products as herbicide formulations and explosives. Several studies identified nitro musk compounds in aquatic environment samples, human milk and fat samples as highly lipophilic and persistent bioaccumulating environmental pollutants. To examine the compounds for genotoxic activity, musk xylene (1-tert.-butyl-3, 5-dimethyl-2, 4, 6-trinitrobenzene), musk ketone (4-tert.-butyl-3, 5-dinitro-2, 6-dimethylacetophenone), musk ambrette (l-tert.-butyl-4-methyl-6-methoxy-3, 5-dinitrobenzene), musk moskene (l, 1, 3, 3, 5-pemamethyl-4, 6-di-nitroindane) and musk tibetene (1-tert.-butyl-3, 4, 5-trimethyl-2, 6-dinitrobenzene) were tested for SOS inducing potency in the SOS chromotest with E. coli PQ37 and for sister-chromatid exchange inducing activities in human lymphocytes in vitro both in the presence and absence of an exogenous metabolizing system from rat liver S9-Mix. Nitro musks revealed no genotoxicity either in the SOS chromotest with E. coli PQ37 or in the sister-chromatid exchange test with human lymphocytes.
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References
Opdyke, D.L.: Musk ambrette. Food Cosm. Toxicol. 13 (1975) 875–876
Opdyke, D.L.: Musk ketone. Food Cosm. Toxicol. 13 (1975) 877–878
Opdyke, D.L.: Musk tibetene. Food Cosm. Toxicol. 13 (1975) 879
Opdyke, D.L.: Musk xylene. Food Cosm. Toxicol. 13 (1975) 881
Opdyke, D.L.: l, l, 3, 3, 5-Pentamethyl-4, 6-dinitroindane. Food Cosm. Toxicol. 13 (1975) 885
Yamagishi, T.;Miyazaki, T.;Horii, S.;Akiyama, K.: Synthetic musk residues in Biota and water from Tama River and Tokyo Bay (Japan). Arch. Environ. Contam. Toxicol. 12 (1983) 83–89
Liebl, B.;Ehrensdorfer, S.: Nitromoschusverbindungen in der Frauenmilch. Gesundh.- Wes. 55 (1993) 527–532
Rimkus, G.;Wolf, M.: Nachweis von Nitromoschusverbindungen in Frauenmilch und Humanfett. Deut. Lebensm.-Rdschau. 89. Jahrg. 4 (1993) 103–107
Rimkus, G.;Wolf, M.: Rückstände und Verunreinigungen in Fischen aus Aquakultur. Deut. Lebensm. -Rdschau. 89. Jahrg. 6 (1993) 171–175
Quillardet, P.;Hofnung, M.: The SOS chromotest, a colorimetric bacterial assay for genotoxins: procedures. Mutat. Res. 147 (1985) 65–78
Hofnung, M.;Quillardet, P.: The SOS chromotest, a colorimetric assay on the primary cellular responses to genotoxic agents. Ann. NY Acad. Sci. 534 (1989) 817–825
Hofnung, M.;Quillardet, P.;Görlich, O.;Touati, E.: SOS chromotest and the use of bacteria for the detection and diagnosis of genotoxic agents. In:Jolles, G.;Cordier, A. New trends in genetic risk assessment. Academic Press, London, (1989) 125–136
Mersch-Sundermann, V.;Kevekordes, S.;Mochayedi, S.: Sources of variability on the Escherichia coli PQ37 genotoxicity assay. Mutat. Res. 252 (1991) 51–60
Mersch-Sundermann, V.;Mochayedi, S.;Kevekordes, S.: Genotoxicity of polycyclic aromatic hydrocarbons inEscherichia coli PQ37. Mutat. Res. 278 (1992) 1–9
Mersch-Sundermann, V.;Wintermann, F.;Kern, S.: Influence of S9-mix composition on the SOS response inEscherichia coli PQ37. Mutat. Res. 291 (1993) 53–60
Mersch-Sundermann, V.;Mochayedi, S.;Kevekordes, S.;Kern, S.;Wintermann, F.: The Genotoxicity of unsubstituted and nitrated polycyclic aromatic hydrocarbons. Anticancer Res 13 (1993) 2037–2044
Mersch-Sundermann, V.;Hofmeister, A.;Müller, G.;Hof, H.: Untersuchungen zur Mutagenität organischer Mikrokontaminationen in der Umwelt, III. Mitteilung: Die Mutagenität ausgewählter Herbizide und Insektizide im SOS chromotest (Makroverfahren). Zbl. Bakt. Hyg., I. Abt. Orig. B 189/2 (1989) 135–146
Mersch-Sundermann, V.;Müller, G.;Hofmeister, A.: Untersuchungen zur Mutagenität organischer Mikrokontaminationen in der Umwelt, IV. Mitteilung: Die Mutagenität leichtflüchtiger Organohalogene im SOS chromotest (Makroverfahren). Zbl. Bakt. Hyg., I. Abt. Orig. B 189 (1989) 266–271
Perry, P.;Wolff, S.: New giemsa method for the differential straining of sister chromatids. Nature 251 (1974) 156
Zakharov, A.F.;Egolina, N.A.: Differential spiralization along mammalian mitotic chromosomes I. BRDU-revealed differentiation in Chinese hamster chromosomes. Chromosoma 38 (1972) 341
Latt, S.A.: Microfluorometric detection of desoxyribonucleid acid replication in human metaphase chromosomes. Proc. Natl. Acad. Sci. 70 (1973) 3395
Lamberti, L.;Brigatti Ponzetto, P.;Ardito, G.: Cell kinetics and sister-chromatid exchange frequency in human lymphocytes. Mutat. Res. 102 (1983) 193
Emig, M.;Reinhardt, A.;Mersch-Sundermann, V.: A comparative study of five nitro musk compounds for genotoxicity in the SOS chromotest and Salmonella mutagenicity. Toxicology Letters 85 (1996)151–156
Mersch-Sundermann, V.;Reinhardt, A.;Emig, M.: Untersuchungen zur Mutagenität, Genotoxicität und Kogenotoxicität umweltrelevanter Nitromoschusverbindungen. Zbl. Hyg. 198 (1996) 429–442
Wild, D.;King, M.T.;Gocke, E.;Eckhardt, K.: Study of artificial flavouring substances for mutagenicity in theSalmonella/Microsome, Basic and Micronucleus Tests. Fd. Chem. Toxic. Vol. 21 (1983) 6: 707–719
Nair, J.;Ohshima, H.;Malaveille, C.;Friesen, M.;O’Neill, K.;Hautefeulle, A.;Bartsch, H.: Identification, occurrence and mutagenicity inSalmonella typhimurium of two synthetic nitroarenes, musk ambrette and musk xylene, in indian chewing tobacco and betel quid. Fd. Chem. Toxic. Vol 24 (1986) 1: 27–31
Quillardet, P.;Hofnung, M.: The SOS chromotest: a review. Mutat. Res. 297 (1993) 235–279
Mersch-Sundermann, V.;Schneider, U.;Klopman, G.;Rosenkranz, H.S.: SOS induction inEscherichia coli and Salmonella mutagenicity: a comparison using 330 compounds. Mutagenesis, vol. 9, no. 2 (1994) 205–224
Mersch-Sundermann, V.;Klopman, G.;Rosenkranz, H.S.: Chemical structure and genotoxicity: studies of the SOS chrootest. Mutat. Res. 340 (1996) 81–91
Mersch-Sundermann, V.;Emig, M.;Reinhardt, A.;Kevekordes, S.: DNA damages, micronucleus formation and P450 enzyme induction by nitro musks. Anticancer Res. 15/5A (1995) 1653–1654
Iwata, N.;Suzuki, K.;Minegishi, K.;Kawanishi, T.;Hara, S.;Endo, T.;Takahashi, A.: Induction of cytochrome P450 1A2 by musk analogues and other inducing agents in rat liver. Eur. J. Pharmacol. 248 (1993)243–250
Lehman-McKeeman, L.D.;Caudill, D.;Young, J.A.;Dierckman, T.A.: Musk xylene induces and inhibits mouse hepatic cytochrome P450 2B enzymes. Biochem. Biophys. Res. Commun., Vol. 206 (1995) 3: 975–980
Maekawa, A.;Matsushima, Y.;Onodera, H.;Shibutani, M.;Ogasawara, H.;Kodama, Y.;Kurokawa, Y.;Hayashi, Y.: Longterm toxicity/carcinogenicity of musk xylol in B6C3F1 mice. Fd. Chem. Toxic. Vol. 28 (1990) 8: 581–586
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Kevekordes, S., Grahl, K., Zaulig, A. et al. Nitro musk compounds genotoxic activity. Environ. Sci. & Pollut. Res. 3, 189–192 (1996). https://doi.org/10.1007/BF02986953
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DOI: https://doi.org/10.1007/BF02986953