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Methyl-thiophanate increases reactive oxygen species production and induces genotoxicity in rat peripheral blood
Ibtissem Ben Amara1, Hajer Ben Saad, Boutheina Cherif
1Animal Physiology Laboratory, Faculty of Sciences, University of Sfax , Tunisia .
Abstract:
Methylthiophanate is one of the widely used fungicides to control important fungal diseases of crops. The aim of this study was to elucidate the short-term hematoxicity and genotoxicity effects of methylthiophanate administered by intraperitoneal way at three doses (300, 500 and 700 mg/kg of body weight) after 24, 48 and 72 h. Our results showed, 24 h after methylthiophanate injection, a hematological perturbation such as red blood cells (p < 0.05, p < 0.05 and p < 0.01) and hemoglobin content (p < 0.05), respectively, and a noticeable genotoxic effect in WBC evidenced by a significant increase in the frequency of the micronuclei and a decrease in cell viability. An increase in erythrocyte osmotic fragility was also noted after 24 and 48 h of methylthiophanate treatment at graded doses. A significant increase in hydrogen peroxide, advanced oxidation of protein products and malondialdehyde levels, in erythrocytes of methylthiophanate-treated rats with 300, 500 and 700 mg/kg of body weight, was also observed after 24 h of treatment (p < 0.05, p < 0.01 and p < 0.001, respectively), suggesting the implication of oxidative stress in its toxicity. Antioxidants activities of superoxide dismutase and glutathione peroxidase in erythrocytes significantly increased (p < 0.001) 24 h after the highest dose injected. While all these parameters were improved after 72 h of methylthiophanate injection (300, 500 and 700 mg/kg body weight). In conclusion, these data showed that the exposure of adult rats to methylthiophanate resulted in oxidative stress leading to hematotoxicity and the impairment of defence system, confirming the pro-oxidant and genotoxic effects of this fungicide.
Insights
Methylthiophanate fungicide causes short-term hematotoxicity and genotoxicity in rats, indicated by blood cell damage and oxidative stress. These adverse effects, including increased oxidative stress markers, were observed 24 hours post-injection but showed improvement after 72 hours.
Area of Science:
- Toxicology
- Environmental Science
- Biochemistry
Background:
- Methylthiophanate is a widely used fungicide for crop disease control.
- Understanding its toxicological profile is crucial for assessing environmental and health risks.
Purpose of the Study:
- To investigate the short-term hematotoxicity and genotoxicity of methylthiophanate in adult rats.
- To elucidate the role of oxidative stress in methylthiophanate-induced toxicity.
Main Methods:
- Adult rats were administered intraperitoneal injections of methylthiophanate at doses of 300, 500, and 700 mg/kg body weight.
- Hematological parameters, erythrocyte osmotic fragility, oxidative stress markers (hydrogen peroxide, advanced oxidation of protein products, malondialdehyde), and antioxidant enzyme activities (superoxide dismutase, glutathione peroxidase) were assessed at 24, 48, and 72 hours post-injection.
- Genotoxicity was evaluated by assessing micronuclei frequency and cell viability in white blood cells (WBC).
Main Results:
- Methylthiophanate administration led to significant hematological perturbations, including decreased red blood cells and hemoglobin content, and increased erythrocyte osmotic fragility at 24 and 48 hours.
- Genotoxic effects were observed in WBC, characterized by increased micronuclei frequency and decreased cell viability.
- Elevated levels of oxidative stress markers and increased antioxidant enzyme activities were noted 24 hours post-treatment, suggesting the involvement of oxidative stress.
- All assessed parameters showed improvement by 72 hours post-injection.
Conclusions:
- Short-term exposure to methylthiophanate induces hematotoxicity and genotoxicity in rats.
- Oxidative stress plays a significant role in the toxic effects of methylthiophanate.
- The fungicide exhibits pro-oxidant and genotoxic properties, impacting the defense system, though recovery is observed within 72 hours.
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