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Toxicity of Secalonic acid D
Journal of Toxicology and Environmental Health
|November 1, 1979
Summary
Secalonic acid D exhibits significant toxicity across different mouse strains and rat models, with varying lethal doses (LD50) depending on administration route and species. Repeated exposure demonstrates cumulative toxicity, leading to mortality and organ damage.
Area of Science:
- Toxicology
- Pharmacology
- Mycotoxin Research
Background:
- Secalonic acid D is a mycotoxin produced by fungi, with potential health implications.
- Understanding its toxicity is crucial for risk assessment and public health.
Purpose of the Study:
- To comprehensively evaluate the toxicity of secalonic acid D using various endpoints.
- To determine lethal dose 50 (LD50) values across different administration routes and animal models.
- To investigate histopathological effects and cumulative toxicity.
Main Methods:
- Determined intraperitoneal (ip) and intravenous (iv) LD50 values in CD-1 mice and Sprague-Dawley rats.
- Assessed oral LD50 values in mice and rats.
- Monitored growth retardation and performed histopathological examinations of affected organs.
- Investigated cumulative toxicity through repeated sublethal dosing.
Main Results:
- IP LD50 values ranged from 27-37 mg/kg in mice and 52 mg/kg in female CD-1 mice.
- IV LD50 was 25 mg/kg in male CD-1 mice; oral LD50 was 400 mg/kg in male CD-1 mice and varied in rats.
- IP administration caused pulmonary atelectasis, peritonitis, and hepatic necrosis; IV administration led to hepatic portal necrosis.
- Cumulative toxicity was observed with repeated sublethal IP doses, with an LD50 of 11.5 mg/kg.
Conclusions:
- Secalonic acid D is acutely toxic, with significant variations in LD50 based on administration route and animal model.
- Histopathological findings indicate multi-organ effects, including pulmonary and hepatic damage.
- Cumulative toxicity highlights the risk associated with repeated exposure to even sublethal doses.