ArticleNaunyn-Schmiedeberg's archives of pharmacology2025
Chlorantraniliprole (Coragen® 20% SC) exposure induced reproductive toxicity mediated by oxidative stress, apoptosis, and sperm quality deficient in male Wistar rats.
Article in Naunyn-Schmiedeberg's archives of pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Insecticides and testicular health: mechanisms of injury and protective natural products.Naunyn-Schmiedeberg's archives of pharmacology · 2025Review
- Calcium Channels and Modulators as Potential Therapeutic Targets for Contraceptives and Male Fertility: A Scoping Review.Open access journal of contraception · 2025Review
Corrections and comments
- Retracted
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pesticides can adversely affect reproduction by causing congenital abnormalities, fetal demise, and infertility. The reproductive toxicity of coragen, a modified ryanodine receptor-targeting insecticide with chlorantraniliprole concentrations of 20%, was examined in male rats. Twenty-one healthy male rats were randomly assigned to one of three groups: the control group, two orally administered with low (500 mg/kg) and high (1000 mg/kg) doses of coragen for 8 weeks. Exposure to coragen resulted in significant, dose-dependent changes in male reproductive hormones, steroidogenic enzymes, and an imbalance in the oxidant-antioxidant system. The treated groups revealed significantly higher lipid peroxidation levels than the control group. The effects were accompanied by damage to testicular tissue, modified testicular lactate dehydrogenase, reduced sperm motility and viability, and heightened sperm abnormalities. Elevated levels of pro-apoptotic proteins (caspase-3 and Bax) and decreased levels of anti-apoptotic protein (Bcl-2) provided evidence of apoptosis in both treatment groups. Moreover, coragen induced substantial DNA damage in the testicular tissue. The results indicate that the reproductive impairment caused by coragen may be ascribed to oxidative stress, hormonal disturbance, apoptosis, and damage to testicular DNA and finally might result in infertility and compromised reproductive function.
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