Soliman Maher M, Nashed Marsail S, Hassanen Eman I, Issa Marwa Y, Prince Abdelbary M, Hussien Ahmed M, Tohamy Adel F
Department of Toxicology and Forensic Medicine, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
Department of Pathology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
Biol Res. 2025 May 6;58(1):27. doi: 10.1186/s40659-025-00605-6.
The purpose of this work was to examine the fundamental mechanisms of reproductive toxicity in rat models following exposure to Fenpropathrin (FNP). Furthermore, our study explores the novel impacts of Date palm kernel extract (DPK) on these detrimental outcomes.
Thirty male Wistar rats were used in the investigation. They were split into six groups: one group received corn oil as a control; two groups received DPK at 200 mg/kg and 400 mg/kg; a group received FNP at 4.7 mg/kg; and two combination groups received DPK and FNP at 200 mg/kg and 400 mg/kg, respectively for 60 days.
FNP caused oxidative stress, reduced sperm count, and impaired motility. FNP decreased the expression of the StAR gene and reduced serum testosterone levels. We assessed the histological alterations. In a dose-dependent way, the concurrent administration of DPK extract successfully decreased all the toxicological parameters.
When taken orally, DPK extract may protect against FNP-induced male reproductive toxicity.
本研究旨在探讨大鼠暴露于甲氰菊酯(FNP)后生殖毒性的基本机制。此外,我们的研究还探索了枣椰核提取物(DPK)对这些有害结果的新影响。
本研究使用了30只雄性Wistar大鼠。它们被分为六组:一组接受玉米油作为对照;两组分别接受200mg/kg和400mg/kg的DPK;一组接受4.7mg/kg的FNP;两组联合组分别接受200mg/kg和400mg/kg的DPK和FNP,持续60天。
FNP导致氧化应激、精子数量减少和活力受损。FNP降低了StAR基因的表达并降低了血清睾酮水平。我们评估了组织学改变。DPK提取物的同时给药以剂量依赖的方式成功降低了所有毒理学参数。
口服时,DPK提取物可能预防FNP诱导的雄性生殖毒性。