Aug 2026· IAA Journal of Biological Sciences· 0 citations
TL;DR
S. aethiopicum leaf extract protected against potassium bromate-induced hepatic dysfunction and inflammatory disturbances, supporting its potential as a natural hepatoprotective and immunomodulatory agent.
Abstract
Potassium bromate (KBr) is a potent oxidizing agent that induces oxidative stress, inflammation, and hepatic injury. This study evaluated the protective effects of Solanum aethiopicum leaf extract against KBr-induced alterations in liver function and inflammatory cytokines in Wistar rats. Thirty Wistar rats (140–150 g) were randomly assigned to five groups (n = 6): normal control, KBr (50 mg/kg), KBr + S. aethiopicum extract (300 mg/kg), KBr + S. aethiopicum extract (600 mg/kg), and KBr + vitamin C (100 mg/kg). Potassium bromate was administered for two weeks before treatment with the extract or vitamin C. Serum liver function indices (total protein, albumin, globulin, ALT, AST, ALP, and total bilirubin) and inflammatory biomarkers (IL-1β and TNF-α) were determined using standard spectrophotometric methods. Data were analyzed using one-way ANOVA followed by Tukey’s post hoc test. Potassium bromate significantly disrupted liver function parameters and reduced (P < 0.05) IL-1β levels compared with the control, indicating hepatic dysfunction and impaired inflammatory homeostasis. Treatment with S. aethiopicum extract significantly restored IL-1β concentrations while maintaining TNF-α levels comparable to the control. The extract also ameliorated KBr-induced alterations in serum proteins and bilirubin. In conclusion, S. aethiopicum leaf extract protected against potassium bromate-induced hepatic dysfunction and inflammatory disturbances, supporting its potential as a natural hepatoprotective and immunomodulatory agent. Further studies are recommended to elucidate its underlying mechanisms of action.
Keywords: inflammation, interleukin-1β, tumor necrosis factor-α, potassium bromate, Solanum aethiopicum.
Potassium bromate (KBrO₃) is a potent oxidizing agent that induces oxidative stress and hepatic injury. This study investigated the protective effects of flavonoids extracted from Solanum aethiopicum leaves against KBrO₃-induced alterations in liver function, antioxidant status, and lipid profile in Wistar rats. Thirty rats were randomly assigned to six groups (n = 5): normal control, S. aethiopicum flavonoids (500 mg/kg), KBrO₃ (50 mg/kg), KBrO₃ + flavonoids (250 mg/kg), and KBrO₃ + flavonoids (500 mg/kg). At the end of the treatment period, serum liver function indices, antioxidant enzymes were determined using standard biochemical methods. Potassium bromate significantly (P < 0.05) reduced serum total protein, albumin, globulin, glutathione peroxidase (GPx), superoxide dismutase (SOD), and catalase (CAT), while significantly increasing alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), total bilirubin, malondialdehyde (MDA). Administration of S. aethiopicum flavonoids significantly reversed these alterations in a dose-dependent manner, with the 500 mg/kg dose showing greater protective effects than the 250 mg/kg dose. The flavonoid extract restored antioxidant enzyme activities, improved liver synthetic and excretory functions. These findings demonstrate that flavonoids extracted from Solanum aethiopicum leaves possess significant hepatoprotective, antioxidant properties against potassium bromate-induced toxicity. The observed protective effects are likely mediated through free radical scavenging, preservation of hepatocyte membrane integrity, and enhancement of endogenous antioxidant defenses. Solanum aethiopicum flavonoids therefore represent a promising natural therapeutic candidate for the prevention and management of oxidative stress-mediated liver dysfunction and associated metabolic disturbances.
Keywords: Hepatoprotective, antioxidants, flavonoids, Solanum aethiopicum, potassium bromate.
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