Sami AHMED, Saeb ABDUL-RAHMAN, Abdullah ABDULMAJEED, Khalid SULTAN
The present study aimed to investigate the antioxidant role of estrogen and its potential protective effect against hydrogen peroxide (H₂O₂)-induced oxidative stress, as well as to evaluate the effects of testosterone on the antioxidant status of liver tissue in male rabbits. Seventy-two adult male rabbits were randomly divided into twelve groups (six animals per group): intact, Intact-H₂O₂, castrated, Castrated-H₂O₂, Intact-H₂O₂-testosterone, Castrated-H₂O₂-testosterone, Intact-H₂O₂-estrogen, Castrated-H₂O₂-estrogen, intact-testosterone, castrated-testosterone, intact-estrogen, and castrated-estrogen. Treatment lasted four weeks. Oxidative stress was induced by adding 0.5% of H2O2 to drinking water. Testosterone (10mg/kg) and estrogen (0.5mg/kg) were injected intramuscularly every other day (3 times/ week). Histopathological examination showed that H₂O₂ exposure caused marked vacuolar degeneration of hepatocytes, congestion of the portal vein, and infiltration of inflammatory cells. Castration partially reduced these alterations by decreasing inflammatory responses. Testosterone administration in H₂O₂-treated rabbits resulted in severe hepatocyte necrosis, degeneration, fibrosis, and increased inflammatory infiltration. In contrast, estrogen treatment significantly reduced hepatocyte necrosis, fibrosis, and inflammatory cell infiltration.