Selenium Could Alleviate Potassium Dichromate-Induced Epididymal, Prostatic and Seminal Vesicle Changes in Adult Rats: Potential Role of Inhibiting NF-κB Pathway | ||||
Egyptian Society of Clinical Toxicology Journal | ||||
Volume 11, Issue 1, June 2023, Page 87-106 PDF (1013.57 K) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/esctj.2023.184880.1025 | ||||
View on SCiNiTO | ||||
Authors | ||||
Manal Mohammad Morsy1; Heba A. Hassan2; Nadia Alabassery3; Rania Saad Ramadan 1 | ||||
1Human Anatomy and Embryology Department, Faculty of Medicine, Zagazig University | ||||
2Clinical Pharmacology Department, Faculty of Medicine, Zagazig Univesity | ||||
3Human Anatomy and Embryology Department, Faculty of Medicine, Zagazig Univesity | ||||
Abstract | ||||
Background: Chromium is generated as a waste product from different industries. Its reproductive toxicity has been addressed in many studies that considered oxidative stress the main contributing factor for such toxicity. Selenium is essential for male reproductive health and crucially involved in regulation of cellular redox status. Aim: To elucidate the potential impacts of potassium dichromate (PDC) on the structure of the epididymis, prostate and seminal vesicles and to investigate the efficacy of selenium on counteracting these impacts. Methods: Thirty-six adult male rats were assigned into four groups: control, selenium, PDC, and PDC+selenium. The animals were subjected for a treatment period of four weeks. At the end of experimental period, blood and semen samples, epididymides, prostates and seminal vesicles were collected and processed for biochemical, morphological and immunohistochemical analyses. Results: PDC administration significantly deteriorated sperm parameters and triggered alteration of cellular redox homeostasis, evidenced by increased serum malonaldehyde levels with decreased enzymatic activity of the antioxidants: superoxide dismutase and catalase. Furthermore, PDC significantly unregulated the expression of the serum inflammatory markers; nuclear factor-kappa B (NF-κB), tumor necrosis factor-alpha and interleuken-1beta. Microscopically, all the examined tissues of PDC-treated rats displayed deteriorated microarchitecture as well as elevated 8-hydroxy-2-deoxyguanosine and microtubule-associated protein light chain3 immunoexpression, indicating increased oxidative DNA damage and autophagy activity. Selenium supplements to PDC-treated rats effectively alleviated all the tested parameters. Conclusion: Selenium supplements could effectively mitigate PDC-induced damage of the epididymis, prostate and seminal vesicles through counteracting oxidative stress, and reducing NF-κB activation and excessive autophagy evoked by PDC. | ||||
Keywords | ||||
Selenium; Chromium; Reprotoxicity; NFκB; Autophagy | ||||
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