Related Experiment Video
Updated: Jul 12, 2026

06:00
Experimental Protocol for Using Drosophila As an Invertebrate Model System for Toxicity Testing in the Laboratory
Published on: July 10, 2018
Genotoxicity is modulated by ascorbic acid. Studies using the wing spot test in Drosophila
Bülent Kaya1, Amadeu Creus, Antonia Velázquez
1Department of Biology, Faculty of Arts and Sciences, Akdeniz University, 07070, Antalya, Turkey.
Mutation Research
|September 26, 2002
Summary
Ascorbic acid (Vitamin C) showed protective effects against potassium dichromate genotoxicity in Drosophila melanogaster. However, it failed to protect against 4-nitroquinoline 1-oxide and unexpectedly increased cobalt chloride genotoxicity.
Area of Science:
- Genetics and Toxicology
- Model Organism Research
Background:
- Ascorbic acid (Vitamin C) is a well-known antioxidant with potential health benefits.
- Understanding its role in modulating genotoxicity is crucial for public health and risk assessment.
- The Drosophila melanogaster wing spot assay (SMART) is a valuable tool for assessing genotoxicity.
Purpose of the Study:
- To investigate the antigenotoxic potential of ascorbic acid (Vitamin C) against three reference mutagens.
- To evaluate the effects of ascorbic acid on the genotoxicity induced by cobalt chloride, 4-nitroquinoline 1-oxide, and potassium dichromate.
Main Methods:
- The study utilized the Drosophila melanogaster wing somatic mutation and recombination test (SMART).
- Larvae were exposed to cobalt chloride (CoCl2), 4-nitroquinoline 1-oxide (4-NQO), and potassium dichromate (K2Cr2O7).
- Co-treatments with varying concentrations of ascorbic acid were performed to assess its modulatory effects.
Main Results:
- All three mutagens (CoCl2, 4-NQO, K2Cr2O7) demonstrated significant genotoxicity in the SMART assay.
- Ascorbic acid effectively reduced the genotoxicity of potassium dichromate to control levels.
- Ascorbic acid showed no antigenotoxic effect against 4-NQO and, unexpectedly, enhanced CoCl2-induced genotoxicity.
Conclusions:
- Ascorbic acid exhibits differential modulatory effects on genotoxicity, acting as a protective agent against potassium dichromate.
- The lack of protection against 4-NQO and the pro-genotoxic effect with cobalt chloride highlight complex interactions.
- Further research is needed to elucidate the mechanisms behind ascorbic acid's varied genotoxicity modulation.
Related Concept Videos
In-vitro Mutagenesis
To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
In vitro Mutagenesis
To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
Mutagenicity and Carcinogenicity
Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for Research on Cancer (IARC) classifies agents into four groups based on their carcinogenic potential. Group 1 agents are known human carcinogens; group 2A agents are probably carcinogenic to humans; group 3 agents lack data to support their role in carcinogenesis; and group 4 includes agents for which data support that they are not likely to be...

