Evaluation of the genotoxic effect of tartrazine using a metabolic activation system in human lymphocyte culture under cytokinetic block conditions

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Abstract

The expansion of the spectrum of use of food additives and, in particular, food dyes (FD), increases the risk of increasing human exposure to genotoxicants. Since in real life, not pure substances with proven genetic safety are in contact with a person, but complex mixtures of unknown composition, even minor impurities in which can become an additional source or modifier of genome instability effects. Of particular concern in this aspect are synthetic FD azo and diazo compounds which can be transformed by human intestinal microflora to some forms of genotoxicants. The purpose of the work is to evaluate the genotoxic effects of 0–2 mg/mL of Tartrazine FD (E102) purchased in a retail network in a micronucleus test on human blood cells cultured under cytokinetic block conditions in parallel in presence and without rat S9 hepatocyte metabolic activation system.

Genotoxic effects were found in cultures without metabolic activation at 0.0000256–0,00064 mg/mL and 0.4 mg/mL of tartrazine, and in the presence of S9 — at 0.0000256 mg/mL, 0,000128 mg/mL and 0.16 mg/mL of tartrazine. For the first time, a dose-dependent suppression of mitotic and proliferative activity of lymphocytes induced by the tested tartrazine sample was revealed, as well as a dose-dependent U-shaped curve in the frequency of apoptosis. The data obtained indicate the presence of genotoxic activity of the studied sample.

We discuss the necessity to create the system for evaluation the genotoxic safety of FD real mixtures from a retail network.

About the authors

Tatyana A. Nikitina

Centre for Strategic Planning and Management of Biomedical Health Risks

Author for correspondence.
Email: TNikitina@cspmz.ru
ORCID iD: 0000-0003-0866-5990
SPIN-code: 9106-5076

biologist, Department of Preventive Toxicology and Biomedical Resear

Russian Federation, Moscow

Mariya A. Konyashkina

Centre for Strategic Planning and Management of Biomedical Health Risks

Email: MKonyashkina@cspmz.ru
ORCID iD: 0000-0002-8319-1329
SPIN-code: 7559-9045
Scopus Author ID: 8142882800

Cand. Sci. (Med.), research associate of the Department of Preventive Toxicology and Biomedical Research

Russian Federation, Moscow

Faina I. Ingel

Centre for Strategic Planning and Management of Biomedical Health Risks

Email: FIngel@cspmz.ru
ORCID iD: 0000-0002-2262-6800
SPIN-code: 1013-7006
Scopus Author ID: 57205760994

Dr. Sci. (Biol.), leading research associate of the Department of Preventive Toxicology and Biomedical Research

Russian Federation, Moscow

Lyudmila V. Akhaltseva

Centre for Strategic Planning and Management of Biomedical Health Risks

Email: LAhalceva@cspmz.ru
ORCID iD: 0000-0002-3619-3858
SPIN-code: 7049-0003
Scopus Author ID: 57138478700

Cand. Sci. (Biol.), senior research associate of the Department of Preventive Toxicology and Biomedical Research

Russian Federation, Moscow

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Supplementary files

Supplementary Files
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1. JATS XML
2. Fig. 1. Total cytogenetic effect of tartrazine without and in the presence of S9. *Differences with own control are significant (χ2, р < 0,5) Частота клеток с генетическими повреждениями, %

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3. Fig. 2. Spectrum of cell populations in human blood cultures exposed to tartrazine without and in the presence of microsomal fraction S9. *Differences between cultivation methods are significant, the χ2 criterion

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4. Fig. 3. Mitotic activity of cells in human blood cultures, exposed to tartrazine in the presence and without of S9

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5. Fig. 4. Changes in the level of apoptosis under the action of tartrazine in the presence of S9 and without it

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Copyright (c) 2023 Nikitina T.A., Konyashkina M.A., Ingel F.I., Akhaltseva L.V.

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This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
 


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