Background Pyrethroids are among the most widely used pesticides worldwide and cause reproductive toxicity through oxidative stress, endocrine disruption, and testicular damage. Numerous studies have explored antioxidant-rich natural products and other bioactive compounds to mitigate the effects of pyrethroid exposure. Purpose This systematic review comprehensively evaluates the evidence on the efficacy of natural products in mitigating pyrethroid-induced reproductive toxicity in experimental models. Methods Following PRISMA guidelines, PubMed, Scopus, Web of Science, and Embase were searched from database inception to July 2025. The animal experimental studies evaluating natural products against pyrethroid-induced reproductive toxicity in adult male laboratory animals were included. Outcomes included sperm parameters, hormonal balance, oxidative stress markers, and testicular histopathology. Study quality and risk of bias were assessed using the ARRIVE guidelines and SYRCLE’s Risk of Bias tool for animal studies, respectively. Results and discussion Thirty-three animal experimental studies were included in this review. Most indicate that pyrethroid exposure consistently decreased sperm count, motility, and testosterone levels, increased oxidative stress, and disrupted the hypothalamic-pituitary-gonadal (HPG) axis. The studies show that natural products such as sage ( Salvia officinalis ), rosemary ( Salvia rosmarinus ), onion ( Allium cepa ), ginseng ( Panax ginseng ), curcumin, quercetin, and resveratrol may ameliorate these effects. Conclusion Proposed mechanisms of natural products include enhanced antioxidant defenses, hormonal regulation, DNA protection, and preservation of testicular, structure although direct evidence for these pathways remains limited and has largely been inferred from a subset of the included studies rather than established as generalizable mechanisms. Nanoparticle formulations may improve bioavailability and efficacy. Natural antioxidants show promise in reducing pyrethroid-induced reproductive toxicity in male experimental animals. Further standardized research and clinical trials are essential to establish translational potential. Systematic Review Registration https://www.crd.york.ac.uk/PROSPERO/ , identifier CRD42022348260.
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Babaei et al. (2026) studied this question.
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