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Acute toxic effects of oxamyl in the rat
1Department of Environmental Toxicology, University of California, Davis 95616.
Abstract:
The effects of single acute oral doses of 1, 2.1, and 3.5 mg/kg oxamyl (a carbamate insecticide) on selected biochemical parameters in male Sprague-Dawley rats were investigated. The animals exhibited significantly decreased weight gain when compared to control animals. The compound inhibited brain and blood acetylcholinesterase significantly in the first few hours of exposure. Liver glucose-6-phosphatase was inhibited substantially after 7 and 4 days at the levels of 2.1 and 3.5 mg/kg, respectively. Maximum inhibition of liver succinic acid dehydrogenase was noted after 1 day at the level of 1 mg/kg and after 6 hr at the level of 2.1 and 3.5 mg/kg. Significant changes in serum total lipids and glucose were observed when oxamyl was given at 2.1 and 3.5 mg/kg, but serum protein was not affected at any dose level. However, the absence of statistically significant effects between Days 7 and 14 in most of the investigated parameters is indicative of an overall moderate degree of toxicity of oxamyl following acute oral administration of the selected doses.
Insights
Acute oral exposure to oxamyl, a carbamate insecticide, caused reduced weight gain and inhibited key enzymes like acetylcholinesterase in rats. Biochemical changes were observed, but most effects lessened by day 14, suggesting moderate toxicity.
Area of Science:
- Toxicology
- Biochemistry
- Environmental Health
Background:
- Oxamyl is a carbamate insecticide widely used in agriculture.
- Carbamates are known to inhibit acetylcholinesterase, an enzyme crucial for nerve function.
- Understanding the biochemical effects of oxamyl is essential for assessing its toxicological profile.
Purpose of the Study:
- To investigate the biochemical effects of acute oral oxamyl exposure in male Sprague-Dawley rats.
- To determine the dose-dependent toxicity and reversibility of oxamyl's effects.
- To evaluate the impact on key enzymes and metabolic parameters.
Main Methods:
- Male Sprague-Dawley rats were administered single acute oral doses of oxamyl (1, 2.1, and 3.5 mg/kg).
- Biochemical parameters including weight gain, acetylcholinesterase, glucose-6-phosphatase, and succinic acid dehydrogenase were measured.
- Serum total lipids, glucose, and protein levels were analyzed at various time points.
Main Results:
- Oxamyl significantly decreased weight gain in exposed rats.
- Inhibition of brain and blood acetylcholinesterase was observed within hours of exposure.
- Dose-dependent inhibition of liver enzymes (glucose-6-phosphatase, succinic acid dehydrogenase) occurred.
- Changes in serum lipids and glucose were noted at higher doses, while serum protein remained unaffected.
- Most biochemical effects showed reduced significance between days 7 and 14.
Conclusions:
- Acute oral oxamyl administration leads to significant biochemical alterations in rats, including enzyme inhibition and changes in metabolic parameters.
- The observed effects, particularly the reduction in enzyme inhibition over time, suggest a moderate overall toxicity of oxamyl at the tested doses.
- These findings contribute to the understanding of oxamyl's toxicological impact and inform risk assessment for potential human or environmental exposure.
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