Literature DB >> 16807077

In vitro genotoxicity of para-phenylenediamine and its N-monoacetyl or N,N'-diacetyl metabolites.

Jean-Luc Garrigue1, Mark Ballantyne, Tirukalikundram Kumaravel, Mel Lloyd, Gerhard J Nohynek, David Kirkland, Hervé Toutain.   

Abstract

para-Phenylenediamine (PPD), a widely used ingredient of oxidative hair dyes, is converted by human hepatocytes and in the human epidermis, or after topical application to rats, to its N-monoacetylated (MAPPD) and/or N,N'-diacetylated (DAPPD) derivatives. We investigated in vitro genotoxic properties of PPD, MAPPD and DAPPD in the Ames test, the micronucleus test (MNT) in human lymphocytes and the mouse lymphoma assay (Hprt locus, PPD only). Given that MAPPD and DAPPD are actual human skin and hepatic metabolites of PPD and represent the substances to which humans are systemically exposed, they were tested in the absence of metabolic activation. In the Ames test, PPD was slightly mutagenic in Salmonella typhimurium strain TA98 in the presence of a rat liver metabolic activation system (S-9), whereas MAPPD and DAPPD were negative in all strains. When tested up to toxic doses, PPD did not induce mutation at the Hprt locus of L5178Y mouse lymphoma cells in two independent experiments, either in the absence or presence of S-9, suggesting that PPD is non-mutagenic in mammalian cells. In the in vitro micronucleus test, PPD induced micronuclei (MN) in cultured human peripheral blood lymphocytes (HL) in the presence of S-9, when tested following 24-h PHA stimulation. No increases in MN frequency were observed in the absence of S-9, when tested following 24-h PHA stimulation. However, PPD induced MN both in the absence and presence of metabolic activation, when tested following 48-h PHA stimulation. In contrast, MAPPD and DAPPD did not induce MN in HL when tested up to 10mM concentrations or to their limit of solubility, respectively, after either 24- or 48-h stimulation. In conclusion, the results of the Ames and MN tests confirm that PPD has a slight genotoxic potential in vitro, although it was non-mutagenic in mammalian cells. Given that MAPPD and DAPPD were negative in the Ames and the MN tests, these acetylated conversion products are considered to be detoxified metabolites that are biologically less reactive than the parent molecule PPD.

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Year:  2006        PMID: 16807077     DOI: 10.1016/j.mrgentox.2006.05.001

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  10 in total

1.  Hair dye use and risk of bladder cancer in the New England bladder cancer study.

Authors:  Stella Koutros; Debra T Silverman; Dalsu Baris; Shelia Hoar Zahm; Lindsay M Morton; Joanne S Colt; David W Hein; Lee E Moore; Alison Johnson; Molly Schwenn; Sai Cherala; Alan Schned; Mark A Doll; Nathaniel Rothman; Margaret R Karagas
Journal:  Int J Cancer       Date:  2011-08-12       Impact factor: 7.396

Review 2.  Xenobiotica-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models.

Authors:  F Oesch; E Fabian; Robert Landsiedel
Journal:  Arch Toxicol       Date:  2018-06-18       Impact factor: 5.153

3.  Effects of Orange II and Sudan III azo dyes and their metabolites on Staphylococcus aureus.

Authors:  Hongmiao Pan; Jinhui Feng; Carl E Cerniglia; Huizhong Chen
Journal:  J Ind Microbiol Biotechnol       Date:  2011-03-31       Impact factor: 3.346

Review 4.  Xenobiotic-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models.

Authors:  F Oesch; E Fabian; K Guth; R Landsiedel
Journal:  Arch Toxicol       Date:  2014-11-05       Impact factor: 5.153

5.  Is there a true concern regarding the use of hair dye and malignancy development?: a review of the epidemiological evidence relating personal hair dye use to the risk of malignancy.

Authors:  Peter Saitta; Christopher E Cook; Jane L Messina; Ronald Brancaccio; Benedict C Wu; Steven K Grekin; Jean Holland
Journal:  J Clin Aesthet Dermatol       Date:  2013-01

Review 6.  Toxicological significance of azo dye metabolism by human intestinal microbiota.

Authors:  Jinhui Feng; Carl E Cerniglia; Huizhong Chen
Journal:  Front Biosci (Elite Ed)       Date:  2012-01-01

7.  Synthetic nickel-containing superoxide dismutase attenuates para-phenylenediamine-induced bladder dysfunction in rats.

Authors:  Bing-Juin Chiang; Tien-Wen Chen; Shiu-Dong Chung; Way-Zen Lee; Chiang-Ting Chien
Journal:  Oncotarget       Date:  2017-11-11

8.  Unveiling the Metabolic Changes on Muscle Cell Metabolism Underlying p-Phenylenediamine Toxicity.

Authors:  Igor Marín de Mas; Silvia Marín; Gisela Pachón; Juan C Rodríguez-Prados; Pedro Vizán; Josep J Centelles; Romà Tauler; Amaya Azqueta; Vitaly Selivanov; Adela López de Ceraín; Marta Cascante
Journal:  Front Mol Biosci       Date:  2017-03-06

9.  Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond.

Authors:  Lidiya Luzhna; Palak Kathiria; Olga Kovalchuk
Journal:  Front Genet       Date:  2013-07-11       Impact factor: 4.599

10.  Determination of phenylenediamines in hair colors derivatizated with 5-(4, 6-dichlorotriazinyl)aminofluorescein via micellar electrokinetic chromatography.

Authors:  Hung-Yu Ko; Yi-Hui Lin; Chi-Jen Shih; Yen-Ling Chen
Journal:  J Food Drug Anal       Date:  2019-03-21       Impact factor: 6.157

  10 in total

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