Affiliation
a All-Russian Scientific Research Institute of Canning Technology, Vidnoe, Russia
b Lomonosov Moscow State University, Moscow, Russia
Copyright ©Samoylov et al. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0. (
http://creativecommons.org/licenses/by/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license.
Received 19 June, 2019 |
Accepted in revised form 02 September, 2019 |
Published 25 February, 2020
Abstract
Negative physiological and biochemical effects of chronic and subchronic doses of benzoates and sorbates may pose a certain risk to human health. Identifying new biomarkers responsible for the body’s response to these compounds could provide significant details in determining the mechanism of their toxicity. To assess comparatively physiological, cytological, cytogenetic, and biochemical parameters in onion roots cells we used an Allium test. The roots were previously treated with sorbic and benzoic acids. The study recorded the dose-dependent toxic effect of these preservatives on the root mass growth. The EC
50 values obtained for benzoic and sorbic acids (10 mg/L and 110 mg/L respectively) were significantly lower than the regulated concentrations prescribed by the standards for their content in certain types of food products. With an increase in concentrations of these acids, the mitotic index of meristematic cells decreased in experimental groups compared to control groups. The data obtained confirmed the necessity of estimating the mitotic index when choosing onion for the Allium test. The necessity resulted from the fact that low proliferative activity could cause false positive results. Sorbic and benzoic acids in concentrations below the corresponding EC
50 increased the frequency of chromosomal aberrations in apical meristematic cells of the roots compared to control. Thus, benzoic and sorbic acids had reliable mitodepressive and genotoxic effects on the dividing cells of onion roots. The study explored the dynamics of lipid oxidation biomarker accumulation (malon dialdehyde, MDA) after exposure to benzoic and sorbic acids. The toxic effect of benzoic acid appeared not to be associated with oxidative damage to root cell lipids, whereas sorbic acid in concentrations from 20 to 200 mg/L resulted in a multiple increase in MDA concentration in the test samples compared to control. At the same time, lipid peroxidation showed a higher level of sensitivity compared to other indicators of this test. Further, the data obtained on the toxic influence of sorbic and benzoic acids can be used in express methods to assess food and ecological security of these acids.
Keywords
Food preservatives,
Allium cepa,
biotesting,
lipid peroxidation toxicity,
cytogenetic analysis,
biomarkers
FUNDING
The materials were prepared as part of the government assignment to V.M. Gorbatov Federal Scientific Center for Food
Systems.
REFERENCES
- Petrov AN, Galstyan AG, Radaeva IA, Turovskaya SN, Illarionova EE, Semipyatniy VK, et al. Indicators of quality of canned milk: Russian and international priorities. Foods and Raw Materials. 2017;5(2):151–161. DOI: https://doi.org/10.21179/2308-4057-2017-2-151-161.
- Strizhko M, Kuznetsova A, Galstyan A, Semipyatniy V, Petrov A, Prosekov A. Development of osmotically active compositions for milk-based products with intermediate humidity. Bulletin of the International Dairy Federation. 2014;35–40.
- Petrov AN, Khanferyan RA, Galstyan AG. Current aspects of counteraction of foodstuff’s falsification. Problems of Nutrition. 2016;85(5):86–92. (In Russ.)
- Prosekov AYu. Fundamentalʹnye osnovy tekhnologii produktov pitaniya [Fundamentals of food technology]. Kemerovo: Kemerovo State University; 2019. 498 p. (In Russ.).
- Prosekov AYu, Ivanova SA. Food security: The challenge of the present. Geoforum. 2018;91:73–77. DOI: https://doi.org/10.1016/j.geoforum.2018.02.030.
- Shu Y, Yu B, He J, Yu J, Zheng P, Yuan ZC, et al. Excess of dietary benzoic acid supplementation leads to growth retardation, hematological abnormality and organ injury of piglets. Livestock Science. 2016;190:94–103.
- Monanu MO, Uwakwe AA, Onwubiko D. In vitro effects of sodium benzoate on the activities of aspartate and alanine amino transferases, and alkaline phosphatase from human erythrocytes of different genotypes. Biokemistri. 2005;17(1):33–38.
- Lok KYW, Chan RSM, Lee VWY, Leung PW, Leung C, Leung J, et al. Food additives and behavior in 8-to 9-yearold children in Hong Kong: A randomized, double-blind, placebo-controlled trial. Journal of Developmental and Behavioral Pediatrics. 2013;34(9):642–650. DOI: https://doi.org/10.1097/DBP.0000000000000005.
- Noorafshan A, Erfanizadeh M, Karbalay-Doust S. Sodium benzoate, a food preservative, induces anxiety and motor impairment in rats. Neurosciences. 2014;19(1):24–28.
- Shahmohammadi M, Javadi M, Nassiri-Asl M. An overview on the effects of sodium benzoate as a preservative in food products. Biotechnology and Health Sciences. 2016;3(3). DOI: https://doi.org/10.17795/bhs-35084.
- Winkler C, Frick B, Schroecksnadel K, Schennach H, Fuchs D. Food preservatives sodium sulfite and sorbic acid suppress mitogen-stimulated peripheral blood mononuclear cells. Food and Chemical Toxicology. 2006;44(12):2003–2007. DOI: https://doi.org/10.1016/j.fct.2006.06.019.
- Blaauboer BJ, Boobis AR, Bradford B, Cockburn A, Constable A, Daneshian M, et al. Considering new methodologies in strategies for safety assessment of foods and food ingredients. Food and Chemical Toxicology. 2016;91:19–35. DOI: https://doi.org/10.1016/j.fct.2016.02.019.
- Wiklund AKE, Adolfsson-Erici M, Liewenborg B, Gorokhova E. Sucralose induces biochemical responses in daphnia magna. PLOS ONE. 2014;9(4).
- Camparoto ML, Teixeira RD, Mantovani MS, Vicentini PVE. Effects of Maytenus ilicifolia Mart. and Bauhinia candicans Benth infusions on onion root-tip and rat bone-marrow cells. Genetics and Molecular Biology. 2002;25(1):85–89. DOI: https://doi.org/10.1590/s1415-47572002000100016.
- Renjana PK, Thoppil JE. Toxicological evaluation of root methanolic extract of Strobilanthes heyneanus nees using Allium test. International Journal of Pharmaceutical Sciences and Drug Research. 2013;5(3):125–128.
- Samoilov AV, Suraeva NM, Zaitseva MV, Kurbanova MN, Stolbova VV. Somparative assessment of artificial sweeteners toxicity via express biotest. Health Risk Analysis. 2019;(2):83–90. (In Russ.). DOI: https://doi.org/10.21668/health.risk/2019.2.09.eng.
- Saghirzadeh M, Gharaati MR, Mohammadi S, Ghiassi-Nejad M. Evaluation of DNA damage in the root cells of Allium cepa seeds growing in soil of high background radiation areas of Ramsar – Iran. Journal of Environmental Radioactivity. 2008;99(10):1698–1702. DOI: https://doi.org/10.1016/j.jenvrad.2008.03.013.
- Hara RV, Marin-Morales MA. In vitro and in vivo investigation of the genotoxic potential of waters from rivers under the influence of a petroleum refinery (Sao Paulo State – Brazil). Chemosphere. 2017;174:321–330. DOI: https://doi.org/10.1016/j.chemosphere.2017.01.142.
- Meng Q, Zou J, Zou J, Jiang W, Liu D. Effect of Su2+ concentration on growth, antioxidant enzyme activity and malondialdehyde content in garlic (Allium sativum L.). Acta Biologica Cracoviensia. Series Botanica. 2007;49(1):95–101.
- Cavusoglu K, Yalcin E, Turkmen Z, Yapar K, Cicek F. Investigation of toxic effects of the glyphosate on Allium cepa. Tarim Bilimleri Dergisi-Journal of Agricultural Sciences. 2011;17(2):131–142.
- Kurbanova MN, Suraeva NM, Rachkova VP, Samoylov AV. Comparative study of indicators of toxic activity in the Allium-test. Agrarian Bulletin of the Urals. 2018;171(4):25–30. (In Russ.).
- Zhang H, Jiang Y, He Z, Ma M. Cadmium accumulation and oxidative burst ingarlic (Allium sativum). Journal of Plant Physiology. 2005;162(9):977–984. DOI: https://doi.org/10.1016/j.jplph.2004.10.001.
- Fiskesjo G. The Allium test as a standard in environmental monitoring. Hereditas. 1985;102(1):99–112. DOI: https://doi.org/10.1111/j.1601-5223.1985.tb00471.x.
- Wibbertmann A, Kielhorn J, Könnecker G, Mangelsdorf I, Melber C. Benzoic acid and sodium benzoate. IPCS Concise International Chemical Assessment Documents; 2000; Geneva. Geneva: World Health Organization; 2000. pp. 49.
- Olufunsho A, da Silva JAT, Akintonwa A. Mitodepressive effect of four food additives using the Allium cepa assay. The African Journal of Plant Science and Biotechnology. 2010;4(1):114–117.
- Pandey H, Kumar V, Roy BK. Assessment of genotoxicity of some common food preservatives using Allium cepa L. as a test plant. Toxicology Reports. 2014;1:300–308. DOI: https://doi.org/10.1016/j.toxrep.2014.06.002.
- Shahin SA, Elamoodi KH. Induction of numerical chromosomal-aberrations during DNA-synthesis using the fungicides nimrod and rubigan-4 in root-tips of Vicia faba L. Mutation Research. 1991;261(3):169–176. DOI: https://doi.org/10.1016/0165-1218(91)90064-s.
- Türkoglu S. Genotoxicity of five food preservatives tested on root tips of Allium cepa L. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 2007;626(1–2):4–14. DOI: https://doi.org/10.1016/j.mrgentox.2006.07.006.
- Zengin N, Yuzbasioglu D, Unal F, Yilmaz S, Aksoy H. The evaluation of the genotoxicity of two food preservatives: Sodium benzoate and potassium benzoate. Food and Chemical Toxicology. 2011;49(4):763–769. DOI: https://doi.org/10.1016/j.fct.2010.11.040.
- Banerjee TS, Giri AK. Effects of sorbic acid and sorbic acid-nitrite in vivo on bone marrow chromosomes of mice. Toxicology Letters. 1986;31(2):101–106. DOI: https://doi.org/10.1016/0378-4274(86)90002-0.
- Jung R, Cojocel C, Muller W, Bottger D, Luck E. Evaluation of the genotoxic potential of sorbic acid and potassium sorbate. Food and Chemical Toxicology. 1992;30(1):1–7. DOI: https://doi.org/10.1016/0278-6915(92)90130-d.
- Yilmaz S, Unal F, Yuzbasioglu D. The in vitro genotoxicity of benzoic acid in human peripheral blood lymphocytes. Cytotechnology. 2009;60(1–3):55–61. DOI: https://doi.org/10.1007/s10616-009-9214-z.
- Hasegawa MM, Nishi Y, Ohkawa Y, Inui N. Effects of sorbic acid and its salts on chromosome-aberrations, sister chromatid exchanges and gene-mutations in cultured chinese-hamster cells. Food and Chemical Toxicology. 1984;22(7):501–507. DOI: https://doi.org/10.1016/0278-6915(84)90219-9.
- Yadav K, Singh NB. Effects of benzoic acid and cadmium toxicity on wheat seedlings. Chilean Journal of Agricultural Research. 2013;73(2):168–174. DOI: https://doi.org/10.4067/S0718-58392013000200013.
- Chrikishvili D, Sadunishvili T, Zaalishvili G. Benzoic acid transformation via conjugation with peptides and final fate of conjugates in higher plants. Ecotoxicology and Environmental Safety. 2006;64(3):390–399. DOI: https://doi.org/10.1016/j.ecoenv.2005.04.009.
- Onyemaobi OI, Williams GO, Adekoya KO. Sytogenetic effects of two food preservatives, sodium metabisulphite and sodium benzoate on the root tips of Allium cepa linn. Ife Journal of Science. 2012;14(1):155–165.
- Iwalokun BA, Oyenuga AO, Saibu GM. Ayorinde J. Analyses of cytotoxic and genotoxic potentials of Loranthus micranthus using the Allium cepa test. Current Research Journal of Biological Sciences. 2011;3(5):459–467.
How to quote?
Samoylov AV, Suraeva NM, Zaytseva MV, Rachkova VP, Kurbanova MN, Petrov AN. Comparative assessment of sorbic and benzoic acid via express biotest. Foods and Raw Materials. 2020;8(1):125–133. DOI: http://doi.org/10.21603/2308-4057-2020-1-125-133