ORIGINAL ARTICLE |
Background: Allium cepa has been linked to a variety of health advantages, although little is known about its hepatoprotective properties. Using biochemical, immunohistochemical, and histological markers, the current study was conducted to examine the efficacy of quercetin-rich aqueous extract of Allium cepa (AEAC) against potassium bromate-induced hepatotoxicity in Wistar rats and the probable mechanism. There are a total of 40 male Wistar rats used in this study and were equally divided into eight (8) groups. Group A: Control. Group B: potassium bromate, KBrO3 (dissolved in water), at 30 mg/kg. Group C: Quercetin as a standard (50 mg/kg). Groups D and E: AEAC, at 300 mg/kg and 150 mg/kg respectively. Groups F and G: KBrO3 plus AEAC. Group H: KBrO3 plus quercetin. On alternate days for 90 days, all administrations were done by intubation.
Results: KBrO3 generated a significant difference in the levels of oxidative stress biomarkers and DNA fragmentation compared to the control (p 0.05). Histological and immunohistochemical examinations of liver samples revealed patterns that were comparable to those seen in enzyme biomarkers. In all cases, combining KBrO3 with AEAC or pure quercetin attenuated the effects of KBrO3.
Conclusion: Therefore, potassium bromate induced hepatocellular toxicity via oxidative stress while treatment with the AEAC ameliorated its effects.
Key words: Allium cepa, Hepatocellular toxicity, Histology, Immunohistochemistry, onion, rats