Document Type
Original Article
Abstract
Background: Cyclophosphamide is anticancer chemotherapeutic drug and immunosuppressive agent for organ transplantation. After its administration, a broad range of negative impacts, involving reproductive toxicity, were observed. The purpose of this research is to evaluate the impact of royal jelly and L-Carnitine on improving the histological and immunohistochemical changes in adult male albino rats that have been exposed to cyclophosphamide-induced testicular cytotoxicity. Material and Methods: Control group 1 (ten rats) and treated group 2 (thirty rats) were separated into three identical subgroups from forty adult male albino rats (a, b, and c). Ten cyclophosphamide-treated rats made up subgroup (a). Ten rats were administered royal jelly with cyclophosphamide in subgroup (b). Subgroup (c): L-carnitine and cyclophosphamide were given to ten rats. The testes were removed and stained with H&E and Masson's trichrome stains, as well as immunohistochemically for detecting bcl-2 proteins, for light microscopic examination. Results: Seminiferous deformed and shrank, with a significant decrease in germinal epithelium thickness that appeared detached from the irregular thick basement membrane and a wide empty lumen devoid of spermatozoa, an increased amount of interstitial tissue, congested blood vessels, and covered by thick tunica albuginea. Royal jelly and L-Carnitine were found to have a significant protective impact against testicular toxicity. Conclusions: Cyclophosphamide produced marked alterations in the royal jelly's histological structure and L-Carnitine had a strong protective impact against the toxicity.
Keywords
cyclophosphamide; royal jelly; L-carnitine; Bcl-2
How to Cite This Article
Swidan, Khalifa; Al-Gharabawi, Gamal; and Abu Emara, Tamer
(2022)
"Impact of royal jelly and L-Carnitine on improving the histological changes of Cyclophosphamide-induced Testicular cytotoxicity in adult male albino rats,"
Al-Azhar International Medical Journal: Vol. 3:
Iss.
7, Article 2.
DOI: https://doi.org/10.21608/aimj.2022.115985.1791