Mitigating effect of gallic acid on zinc oxide nanoparticles and arsenic trioxide-induced spermatogenesis suppression, testicular injury, hormonal imbalance, and immunohistochemical changes in rats

• Published in: Naunyn-Schmiedeberg's archives of pharmacology 2024-12, Vol.397 (12), p.9859-9875
• Main Authors: Behairy, Amany, Hashem, Mohamed M. M., Abo-EL-Sooud, Khaled, El-Metwally, Abeer E., Soliman, Ahmed M., Mouneir, Samar M., Hassan, Bayan A., Abd-Elhakim, Yasmina M.
• Format: Article
• Language: English
• Subjects: 17β-Estradiol; Animals; Antioxidants - pharmacology; Arsenic; Arsenic trioxide; Arsenic Trioxide - toxicity; Biomedical and Life Sciences; Biomedicine; Follicle Stimulating Hormone - blood; Gallic acid; Gallic Acid - pharmacology; Glutathione peroxidase; Luteinizing hormone; Luteinizing Hormone - blood; Male; Nanoparticles; Neurosciences; Nitric Oxide Synthase Type II - metabolism; Nitric-oxide synthase; Oxidants; Oxidative stress; Oxidative Stress - drug effects; Pharmacology/Toxicology; Proliferating cell nuclear antigen; Proliferating Cell Nuclear Antigen - metabolism; Prostate; Rats; Rats, Sprague-Dawley; Seminal vesicle; Serum levels; Spermatogenesis; Spermatogenesis - drug effects; Testes; Testis - drug effects; Testis - metabolism; Testis - pathology; Testosterone; Testosterone - blood; Zinc oxide; Zinc Oxide - toxicity; Zinc oxides
• ISSN: 0028-1298; 1432-1912; 1432-1912
• DOI: 10.1007/s00210-024-03228-y

The current study compared the effects of incorporated exposure to arsenic trioxide (As) and zinc oxide nanoparticles (ZnONPs) on male reproductive hormones, oxidative stress, and inflammatory biomarkers in adult rats to each metal alone. A defensive trial with gallic acid (GA) has also been studied. A total of 60 adult male Sprague Dawley rats were categorized into six groups: control, GA (20 mg/kg), ZnONPs (100 mg/kg), As (8 mg/kg), ZnONPs with As, and GA concurrently with ZnONPs and As at the same previous doses. The regimens were applied for 60 days in sequence. Current findings showed significant weight loss in all study groups, with testicular weights significantly decreased in the As and combined groups. Testosterone, follicular stimulating hormone, and luteinizing hormone serum levels were also considerably reduced, while serum levels of estradiol increased. Inducible nitric oxide synthase (iNOS) immunoexpression was significantly upregulated while proliferating cell nuclear antigen (PCNA) was downregulated. Moreover, there was a significant elevation of testicular malondialdehyde, reduction of testicular superoxide dismutase, and glutathione peroxidase with disruptive testes, prostate glands, and seminal vesicle alterations in all experimental groups with marked changes in the combined group. Additionally, the present results revealed the protective effects of GA on ZnONPs and As adverse alterations in rats. GA enhanced sperm picture, oxidant status, and hormonal profile. Also, it modulates iNOS and PCNA immunoexpression and recovers the histoarchitecture of the testes, prostate glands, and seminal vesicles. Ultimately, GA may be a promising safeguarding agent against ZnONPs and As-induced disturbances to reproductive parameters .