Mostafa-Hedeab Gomaa, Behairy Amany, Abd-Elhakim Yasmina M, Mohamed Amany Abdel-Rahman, Noreldin Ahmed E, Dahran Naief, Gaber Rasha A, Alqahtani Leena S, Essawi Walaa M, Eskandrani Areej A, El-Shetry Eman S
Pharmacology Department & Health Research Unit, Medical College, Jouf University, Sakaka 72446, Saudi Arabia.
Department of Physiology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44511, Egypt.
Antioxidants (Basel). 2023 Feb 2;12(2):361. doi: 10.3390/antiox12020361.
This study assessed the possible protective role of green synthesized zinc oxide nanoparticles using leaf extract (MO-ZNPs) in acrylamide (ACR)-induced reproductive dysfunctions in male rats. ACR (20 mg/kg b.wt/day) and/or MO-ZNPs (10 mg/kg b.wt/day) were given orally by gastric gavage for 60 days. Then, sperm parameters; testicular enzymes; oxidative stress markers; reproductive hormones including testosterone, luteinizing hormone (LH)-estradiol, and follicle-stimulating hormone (FSH) concentration; testis histology; steroidogenesis-related gene expression; and apoptotic markers were examined. The findings revealed that MO-ZNPs significantly ameliorated the ACR-induced decline in the gonadosomatic index and altered the pituitary-gonadal axis, reflected by decreased serum testosterone and FSH with increased estradiol and LH, and sperm analysis disruption. Furthermore, a notable restoration of the tissue content of antioxidants (catalase and reduced glutathione) but depletion of malondialdehyde was evident in MO-ZNPs+ACR-treated rats compared to ACR-exposed ones. In addition, MO-ZNPs oral dosing markedly rescued the histopathological changes and apoptotic caspase-3 reactions in the testis resulting from ACR exposure. Furthermore, in MO-ZNPs+ACR-treated rats, ACR-induced downregulation of testicular steroidogenesis genes and proliferating cell nuclear antigen (PCNA) immune-expression were reversed. Conclusively, MO-ZNPs protected male rats from ACR-induced reproductive toxicity by suppressing oxidative injury and apoptosis while boosting steroidogenesis and sex hormones.
本研究评估了使用叶提取物绿色合成的氧化锌纳米颗粒(MO-ZNPs)对丙烯酰胺(ACR)诱导的雄性大鼠生殖功能障碍可能具有的保护作用。通过胃管饲法口服给予ACR(2毫克/千克体重/天)和/或MO-ZNPs(10毫克/千克体重/天),持续60天。然后,检测精子参数、睾丸酶、氧化应激标志物、包括睾酮、黄体生成素(LH)-雌二醇和促卵泡激素(FSH)浓度在内的生殖激素、睾丸组织学、类固醇生成相关基因表达以及凋亡标志物。研究结果显示,MO-ZNPs显著改善了ACR诱导的性腺指数下降,并改变了垂体-性腺轴,表现为血清睾酮和FSH降低,雌二醇和LH升高,以及精子分析结果异常。此外,与仅暴露于ACR的大鼠相比,在MO-ZNPs+ACR处理的大鼠中,抗氧化剂(过氧化氢酶和还原型谷胱甘肽)的组织含量显著恢复,但丙二醛含量减少。另外,口服MO-ZNPs明显挽救了ACR暴露导致的睾丸组织病理学变化和凋亡性半胱天冬酶-3反应。此外,在MO-ZNPs+ACR处理的大鼠中,ACR诱导的睾丸类固醇生成基因下调和增殖细胞核抗原(PCNA)免疫表达得到逆转。总之,MO-ZNPs通过抑制氧化损伤和细胞凋亡,同时促进类固醇生成和性激素分泌,保护雄性大鼠免受ACR诱导的生殖毒性。