Related Experiment Video
Updated: Mar 6, 2026

A Microplate Assay to Assess Chemical Effects on RBL-2H3 Mast Cell Degranulation: Effects of Triclosan without Use of an Organic Solvent
Published on: November 1, 2013
Effects of tartrazine on proliferation and genetic damage in human lymphocytes
Zülal Atlı Şekeroğlu1, Büşra Güneş1, Seval Kontaş Yedier1
1a Department of Biology, Faculty of Science and Letters , Ordu University , Ordu , Turkey.
Abstract:
The color additive, tartrazine (TRZ), is widely used in food products, drugs and cosmetics. Genotoxicity of TRZ and its metabolites has not been investigated in detail in the presence and absence of a metabolic activator (S9 mix) in human. Therefore, the aim of this study is to investigate the cytotoxic and genotoxic effects of TRZ and its metabolites on cultured human lymphocytes by using chromosome aberration (CA) and micronucleus (MN) tests. Cultures were treated with 625, 1250 and 2500 μg/ml of TRZ in the presence and absence of S9 mix. TRZ showed cytotoxic activity at the highest concentration due to significant decrease in mitotic index (MI) in the absence of S9 mix when compared with solvent control. TRZ and metabolites significantly increased the CAs and aberrant cells in the presence and absence of S9 mix at the higher concentrations. Increased MN values in cultures with and without S9 mix were found to significantly at the highest concentration when tested. Our results indicated that while both TRZ and its metabolites have genotoxic potential on human lymphocyte cultures with and without S9 mix, TRZ can induce cytotoxicity at the highest concentration in culture without S9 mix under the experimental conditions.
Insights
The food additive tartrazine (TRZ) and its metabolites show genotoxic potential in human cells. TRZ also demonstrated cytotoxicity at high concentrations without metabolic activation.
Area of Science:
- Toxicology
- Genetics
- Food Science
Background:
- Tartrazine (TRZ) is a widely used color additive in food, drugs, and cosmetics.
- The genotoxicity of TRZ and its metabolites, particularly in human systems with metabolic activation, requires further investigation.
Purpose of the Study:
- To assess the cytotoxic and genotoxic effects of TRZ and its metabolites on cultured human lymphocytes.
- To evaluate these effects in the presence and absence of a metabolic activator (S9 mix).
Main Methods:
- Cultured human lymphocytes were treated with varying concentrations of TRZ (625, 1250, 2500 μg/ml).
- Tests included chromosome aberration (CA) and micronucleus (MN) assays.
- Experiments were conducted both with and without the addition of S9 mix.
Main Results:
- TRZ exhibited cytotoxic activity at the highest concentration (2500 μg/ml) by decreasing the mitotic index (MI) in the absence of S9 mix.
- Both TRZ and its metabolites significantly increased chromosome aberrations (CAs) and aberrant cells at higher concentrations, with or without S9 mix.
- Elevated micronucleus (MN) values were observed at the highest TRZ concentration in both conditions.
Conclusions:
- Tartrazine and its metabolites possess genotoxic potential in human lymphocyte cultures.
- TRZ can induce cytotoxicity at high concentrations, especially without metabolic activation (S9 mix).
- Further research into the safety of TRZ is warranted.
More Related Videos
05:27Gap Junctional Intercellular Communication: A Functional Biomarker to Assess Adverse Effects of Toxicants and Toxins, and Health Benefits of Natural Products
Published on: December 25, 2016
06:25Chromosomics: Detection of Numerical and Structural Alterations in All 24 Human Chromosomes Simultaneously Using a Novel OctoChrome FISH Assay
Published on: February 6, 2012
Related Concept Videos
Mutagenicity and Carcinogenicity
Toxicity Testing in Animals