Edo Great Iruoghene, Onoharigho Favour Ogheneoruese, Jikah Agatha Ngukuran, Agbo Joy Johnson
Department of Chemistry, Faculty of Science, Delta State University of Science & Technology, Ozoro, Nigeria.
Department of Biochemistry, Faculty of Science, Elizade University, Ilara-Mokin, Nigeria.
Drug Chem Toxicol. 2025 Jan;48(1):98-106. doi: 10.1080/01480545.2024.2362891. Epub 2024 Jun 5.
Plants are a rich source of antioxidants that are produced naturally. Therefore, this study was aimed to evaluate the effect of the plant in the attenuation of paracetamol (PCM) hepatotoxicity in Wistar rats. Twenty-four male albino Wistar rats weighing between 200 and 250 g were divided into four groups, with six rats each. Group 1 served as the control group, receiving just distilled water. Groups 2 and 3 received orally 250 mg/kg bwt/day PCM and 300 mg/kg bwt/day methanol extract of leaves for two weeks, respectively. For group 4, the leaf extract was pre-administered for 1 week before receiving 300 mg/kg bwt/day leaves extract and 250 mg/kg bwt/day PCM for 2 weeks. As a marker of liver damage, serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were measured. Liver tissue reduced glutathione (GSH) concentration, superoxide dismutase (SOD), glutathione-S-transferase (GST), and catalase activities were utilized to determine antioxidant state, while malondialdehyde (MDA) concentration was employed as a lipid peroxidation indicator. When compared to the control group, the activities of serum AST, ALT, SOD, and MDA levels were considerably ( < 0.05) higher in the PCM group, although GSH level and GST and catalase activities were significantly lower. In comparison to the PCM group, co-administration of PCM with extract decreased serum AST and ALT activities. This study shows that the leaf extracts of protects Wistar rats' livers from PCM-induced oxidative stress by increasing antioxidant enzymes.
植物是天然产生的抗氧化剂的丰富来源。因此,本研究旨在评估该植物对Wistar大鼠扑热息痛(PCM)肝毒性的减轻作用。将24只体重在200至250克之间的雄性白化Wistar大鼠分为四组,每组六只。第1组作为对照组,仅接受蒸馏水。第2组和第3组分别口服250毫克/千克体重/天的PCM和300毫克/千克体重/天的叶甲醇提取物,持续两周。对于第4组,在接受300毫克/千克体重/天的叶提取物和250毫克/千克体重/天的PCM两周之前,先给予叶提取物1周。作为肝损伤的标志物,测量了血清天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)。利用肝组织还原型谷胱甘肽(GSH)浓度、超氧化物歧化酶(SOD)、谷胱甘肽-S-转移酶(GST)和过氧化氢酶活性来确定抗氧化状态,同时将丙二醛(MDA)浓度用作脂质过氧化指标。与对照组相比,PCM组血清AST、ALT、SOD和MDA水平的活性显著(P<0.05)更高,尽管GSH水平以及GST和过氧化氢酶活性显著更低。与PCM组相比,PCM与提取物联合给药降低了血清AST和ALT活性。本研究表明,该植物的叶提取物通过增加抗氧化酶来保护Wistar大鼠的肝脏免受PCM诱导的氧化应激。