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Testicular toxicity of profenofos in matured male rats
Gihan Gamal Moustafa1, Zein Shaban Ibrahim, Yoshiharu Hashimoto
1Laboratory of Toxicology, Department of Environmental Veterinary Sciences, Graduate School of Veterinary Medicine, Hokkaido University, N18, W9, Kita-ku, Sapporo, 060-0818, Japan.
Abstract:
To investigate the effect of the phosphorothoate insecticide profenofos on male specific gene expression on rat testis, 16-week-old Wistar rats were orally administered at dose of 17.8 mg/kg twice weekly for 65 days. Gene expression in the testes was monitored by DNA microarray analysis and real-time RT-PCR, which revealed that genes related to steroidogenesis including cytochrome P450 17A1 (CYP17A1), steroidogenic acute regulatory protein (StAR) and CYP11A1 were significantly increased. Besides the testes were histopathologicaly examined, which revealed testicular destruction and degeneration represented by a layer of columnar epithelium, oedematous changes surrounding the seminiferous tubules besides vacuolated spermatogonial cells and more elongated Leydig cells. These data suggest that profenofos considered as one of the male reproductive toxicants. Furthermore, we propose that the above three steroidogenic-related genes and the gene of acrosomal reaction as potential biomarkers of testicular toxicity.
Insights
The insecticide profenofos significantly increased male-specific steroidogenesis genes in rat testes, causing testicular damage. These genes, along with the acrosomal reaction gene, may serve as biomarkers for profenofos-induced testicular toxicity.
Area of Science:
- Toxicology
- Reproductive Biology
- Molecular Biology
Background:
- Organophosphate insecticides like profenofos are widely used in agriculture.
- Exposure to environmental toxicants can disrupt male reproductive health.
- Understanding the molecular mechanisms of insecticide toxicity is crucial for risk assessment.
Purpose of the Study:
- To investigate the impact of profenofos exposure on male rat reproductive gene expression.
- To identify potential molecular biomarkers for profenofos-induced testicular toxicity.
Main Methods:
- 16-week-old Wistar rats were orally administered profenofos (17.8 mg/kg) twice weekly for 65 days.
- Gene expression analysis using DNA microarray and real-time RT-PCR.
- Histopathological examination of testicular tissues.
Main Results:
- Profenofos significantly upregulated genes involved in steroidogenesis: cytochrome P450 17A1 (CYP17A1), steroidogenic acute regulatory protein (StAR), and CYP11A1.
- Histopathology revealed testicular destruction, degeneration, vacuolated spermatogonial cells, and elongated Leydig cells.
- Increased expression of genes related to steroidogenesis and acrosomal reaction.
Conclusions:
- Profenofos acts as a male reproductive toxicant, inducing significant testicular damage.
- Upregulated steroidogenic genes (CYP17A1, StAR, CYP11A1) and the acrosomal reaction gene are proposed as potential biomarkers for testicular toxicity.
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