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Updated: Sep 21, 2026

Transgenic Rodent Assay for Quantifying Male Germ Cell Mutant Frequency
Published on: August 6, 2014
Cytogenetic effects of malathion insecticide on somatic and germ cells of mice
D M Salvadori1, L R Ribeiro, C A Pereira
1Serviço de Genética, Instituto Butantan, São Paulo, Brasil.
Abstract:
Male mice dermally exposed to single or multiple treatment (5 days/2 weeks) showed that the ability of malathion to induce chromosome aberrations in somatic (bone marrow) and germ cells (primary spermatocytes) was related to the type of treatment and dose used. Statistically significant increases of chromosome aberrations in bone marrow cells occurred after single treatment (500 and 2000 mg/kg body wt) when chromatid gaps were included and after multiple treatment (250 and 500 mg/kg) when they were excluded. No dose-response relationships were observed for either treatment. In germ cells, malathion induced a significant increase of univalents in both types of treatment but structural chromosome aberrations were induced only by multiple treatment. Malathion induced a significant decrease of the mitotic indices in the bone marrow.
Insights
Malathion exposure caused chromosome damage in male mice, affecting both somatic and germ cells. The extent of damage depended on the treatment type and dosage, with no clear dose-response observed.
Area of Science:
- Toxicology
- Genetics
- Environmental Health
Background:
- Malathion is a widely used organophosphate insecticide.
- Pesticides can pose risks to non-target organisms, including humans.
- Understanding the genotoxic potential of malathion is crucial for risk assessment.
Purpose of the Study:
- To investigate the genotoxicity of malathion in male mice.
- To evaluate chromosome aberrations in somatic and germ cells following dermal exposure.
- To determine the influence of single versus multiple exposure regimens on malathion's effects.
Main Methods:
- Male mice were dermally exposed to malathion at various doses.
- Chromosomal aberrations in bone marrow cells (somatic) and primary spermatocytes (germ cells) were analyzed.
- Mitotic indices in bone marrow were assessed.
Main Results:
- Malathion induced significant chromosome aberrations in bone marrow cells, particularly with single high-dose or multiple lower-dose treatments.
- Germ cell analysis revealed increased univalents with both treatment types and structural aberrations with multiple treatments.
- A significant decrease in mitotic indices was observed in bone marrow cells.
Conclusions:
- Dermal exposure to malathion can induce genotoxic effects in male mice.
- The type of exposure (single vs. multiple) and dose influence the observed chromosomal damage.
- Malathion's genotoxicity warrants further investigation, especially concerning reproductive health.
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