Related Experiment Video
Updated: Aug 11, 2026

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
Genotoxic and aneugenic properties of an imidazole derivative
M A Carballo1, A S Hick, S Soloneski
1Citogenética y Genética Toxicológica. Departamento de Bioquímica Clínica, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Argentina. macarballo2003@yahoo.com.ar
Abstract:
To contribute to a more accurate characterization of the mutagenic and aneugenic effects of thiabendazole (TBZ), a widely used antiparasitic and food preservative drug, the induction of sister chromatid exchanges (SCEs) and mitotic spindle anomalies as cytogenetic end-points were investigated. Studies were carried out in Chinese hamster ovary (CHO) cells and human peripheral blood lymphocytes. A significant dose-dependent increase in SCE frequency was observed in CHO cells with S9-Mix (P < 0.01) in the 50-100 microg ml(-1) dose-range, while in the absence of S9-Mix, an enhancement of the SCE frequency was exhibited at the highest dose (P < 0.01). In CHO-K1 cells a significant increase in mitotic spindle anomalies (P < 0.01) was observed with the highest concentration assayed reflecting the specific effect of TBZ formulation at the microtubule level. Cell proliferation kinetics (CPK) were not modified by the addition of this pharmaceutical product. In human lymphocyte cultures, exposure to 100 microg ml(-1) TBZ formulation resulted in a significant decrease of the mitotic index (MI) (P < 0.003) and changes in the replication index (RI) (P < 0.05).
Insights
Thiabendazole (TBZ) can induce genetic damage, increasing sister chromatid exchanges in hamster cells and affecting cell division in human lymphocytes. Further research is needed to fully understand its mutagenic and aneugenic potential.
Area of Science:
- Cytogenetics
- Toxicology
- Molecular Biology
Background:
- Thiabendazole (TBZ) is a widely used antiparasitic and food preservative.
- Understanding its mutagenic and aneugenic effects is crucial for public health.
- Cytogenetic endpoints provide valuable insights into genotoxicity.
Purpose of the Study:
- To investigate the mutagenic and aneugenic potential of thiabendazole (TBZ).
- To characterize the induction of sister chromatid exchanges (SCEs) and mitotic spindle anomalies.
- To assess TBZ's effects in both Chinese hamster ovary (CHO) cells and human peripheral blood lymphocytes.
Main Methods:
- Exposure of CHO cells and human lymphocytes to varying concentrations of TBZ.
- Analysis of sister chromatid exchange (SCE) frequency.
- Assessment of mitotic spindle anomalies and cell proliferation kinetics (CPK).
- Evaluation of mitotic index (MI) and replication index (RI) in human lymphocytes.
Main Results:
- A dose-dependent increase in SCE frequency was observed in CHO cells, particularly with S9-Mix.
- Significant induction of mitotic spindle anomalies was noted in CHO-K1 cells at higher TBZ concentrations.
- Human lymphocyte cultures showed a decreased mitotic index (MI) and altered replication index (RI) upon TBZ exposure.
- Cell proliferation kinetics (CPK) remained unaffected in CHO cells.
Conclusions:
- Thiabendazole (TBZ) exhibits mutagenic and aneugenic properties, evidenced by increased SCEs and spindle anomalies in vitro.
- TBZ can disrupt cell division processes in human lymphocytes.
- The findings highlight the need for careful consideration of TBZ's genotoxic potential in its applications.
Related Concept Videos
Mutagenicity and Carcinogenicity
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
Physical Properties of Amines
Teratogenicity
Chemotherapy-Induced Nausea and Vomiting: 5-HT3 Receptor Antagonists
Chemotherapy-Induced Nausea and Vomiting: Dopamine Receptor Antagonists
Phenothiazines, such as prochlorperazine...
