Journals / Turkish Journal of Biology / 2010 / Cilt: 34 - Sayı: 1

In Vitro Genotoxic Effects of Benzoyl Peroxide in Human Peripheral Lymphocytes

Pages
15–24
Publication Date
2010-01-01
DOI
—
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

Statistically significant reductions in the proliferation index (PI) and mitotic index (MI) were only detected in cultures for the 48-h treatment period.

📌 3 Key Takeaways

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Objective & Hypothesis:The aim of the present research was to investigate the genotoxic potency of benzoyl peroxide (BPO), a whitener of flour and cheese, using in vitro sister chromatid exchange (SCE), chromosome aberration (CA), and micronucleus (MN) tests in human peripheral lymphocytes.
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Key Findings & Data:Cells were exposed to 25, 50, 75, and 100 µg/mL concentrations of BPO for 24 and 48 h.
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Conclusion & Impact:Statistically significant reductions in the proliferation index (PI) and mitotic index (MI) were only detected in cultures for the 48-h treatment period.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: Benzoyl peroxide · human lymphocytes · sister chromatid exchange

Abstract

The aim of the present research was to investigate the genotoxic potency of benzoyl peroxide (BPO), a whitener of flour and cheese, using in vitro sister chromatid exchange (SCE), chromosome aberration (CA), and micronucleus (MN) tests in human peripheral lymphocytes. Cells were exposed to 25, 50, 75, and 100 µg/mL concentrations of BPO for 24 and 48 h. BPO induced SCEs only at the highest concentration (100 µg/mL) for 48 h treatment. Furthermore, BPO induced CAs at 75 and 100 µg/mL concentrations for 24 h treatment, and at all concentrations for 48 h treatment. BPO induced CAs in a dose-dependent manner for 24 and 48 h treatment periods. Increased level of MN formation induced by BPO was only observed for the 48 h treatment period at the 2 highest concentrations (75 and 100 µg/mL). Statistically significant reductions in the proliferation index (PI) and mitotic index (MI) were only detected in cultures for the 48-h treatment period.

Özet

The aim of the present research was to investigate the genotoxic potency of benzoyl peroxide (BPO), a whitener of flour and cheese, using in vitro sister chromatid exchange (SCE), chromosome aberration (CA), and micronucleus (MN) tests in human peripheral lymphocytes. Cells were exposed to 25, 50, 75, and 100 µg/mL concentrations of BPO for 24 and 48 h. BPO induced SCEs only at the highest concentration (100 µg/mL) for 48 h treatment. Furthermore, BPO induced CAs at 75 and 100 µg/mL concentrations for 24 h treatment, and at all concentrations for 48 h treatment. BPO induced CAs in a dose-dependent manner for 24 and 48 h treatment periods. Increased level of MN formation induced by BPO was only observed for the 48 h treatment period at the 2 highest concentrations (75 and 100 µg/mL). Statistically significant reductions in the proliferation index (PI) and mitotic index (MI) were only detected in cultures for the 48-h treatment period.

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Cite This Article

YAVUZ, A., TOPAKTAŞ, M., *, -., İSTİFLİ, E. S. (2010). In Vitro Genotoxic Effects of Benzoyl Peroxide in Human Peripheral Lymphocytes. Turkish Journal of Biology, Cilt: 34 - Sayı: 1, 15–24. https://ajindex.com/articles/182449

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References (16)

  1. Binder RL, Aardema MJ, Thompson ED. Benzoyl peroxide: review of experimental carcinogenesis and human safety data. Prog Clin Biol Res 391: 245-94, 1995
  2. Ishidate M. JR, Sofuni T, Yoshikawa K et al. Primary mutagenicity screening of food additives currently used in Japan. Food Chem Toxicol 22: 623-36, 1984
  3. SIDnitial assessment report for SIAM 15; 22-25 October 2002, Boston, USA. (www.inchem.org/documents/sids/sids/ BENZOYLPER.pdf
  4. Dillon D, Combes R, Zeiger E. The effectiveness of Salmonella strains TA100, TA102 and TA104 for detecting mutagenicity of some aldehydes and peroxides. Mutagenesis 13: 19-26, 1998
  5. Epstein SS, Arnold E, Andrea J et al. Detection of chemical mutagens by the dominant lethal assay in the mouse. Toxicol Appl Pharmacol 23: 288-325, 1972
  6. Speit G, Haupter S. On the mechanism of differential giemsa staining of bromodeoxyuridine substituted chromosomes. II. Differences between the demonstration of sister chromatid differentiation replication patterns. Hum Genet 70: 126-129, 1985
  7. Mitelman F, editor. ISCN: An International System for Human Cytogenetic Nomenclature. Basel, Switzerland: S. Karger; 1995
  8. Paz-y-Miño C, Bustamante G, Sanchez ME et al. Cytogenetic monitoring in a population occupationally exposed to pesticides in Ecuador. Environ Health Perspect 110: 1077-1080, 2002
  9. Mace ML Jr, Daskal Y, Wray W. Scanning electron microscopy of chromosome aberrations. Mutat Res 52: 199-206, 1978
  10. Rothfuss A, Schutz P, Bochum S et al. Induced micronucleus frequencies in peripheral lymphocytes as a screening test for carriers of a BRCA1 mutation in breast cancer families. Cancer Res 60: 390-394, 2000
  11. Titenko-Holland N, Windham G, Kolachana P et al. Genotoxicity of malathion in human lymphocytes assessed using the micronucleus assay in vitro and in vivo: a study of malathion-exposed workers. Mutat Res 388: 85-95, 1997
  12. Fenech M, Morley AA. Measurement of micronuclei in lymphocytes. Mutat Res 147: 29-36, 1985
  13. Kaya FF, Topaktaş M. Genotoxic effects of potassium bromate on human peripheral lymphocytes in vitro. Mutat Res 626: 48- 52, 2007
  14. Tsuda H, Kushi A, Yoshida D et al. Chromosomal aberrations and sister-chromatid exchanges induced by gaseous nitrogen dioxide in cultured Chinese hamster cells. Mutat Res 89: 303-9, 1981
  15. Yadav JS, Seth N. Effect of NOx on the somatic chromosomes of goldsmiths. Environ Health Perspect 106: 643-7, 1998
  16. Fujie K, Shimazu H, Matsuda M et al. Acute cytogenetic e