Experimental Pharmacology and Toxicology, Faculty of Pharmaceutical Sciences, University of Port Harcourt, Choba, PMB 5323 Port Harcourt, Rivers State, Nigeria.
Medical Laboratory Sciences, Faculty of Basic Medical Sciences, College of Health Sciences, Niger Delta University, Amassoma, PMB 071 Yenegoa, Bayelsa State, Nigeria.
J Integr Med. 2019 Jan;17(1):46-56. doi: 10.1016/j.joim.2018.11.008. Epub 2018 Dec 1.
Drug-induced liver injury complicates antituberculosis drug treatment and is a leading cause of death worldwide. The aim of this study is to establish the ethnomedicinal claim of hepatoprotective effects of fruit pulp extract of Telfairia occidentalis against rifampicin (RIF) and isoniazid (INH)-induced oxidative stress in rats.
T. occidentalis pulp extract (TOPE) (125-500 mg/kg) and silymarin (50 mg/kg) were evaluated in an induced hepatotoxicity model of oxidative stress in Wistar rats by intoxication with RIF and INH (100 mg/kg each) orally for 60 d. Markers indicating oxidative stress and hepatic damage such as alanine aminotransferase (ALT), aspartate aminotransferase (AST) and alkaline phosphatase (ALP) were assessed. Biomarkers of antioxidant status, including catalase, glutathione reductase, glutathione peroxidase and superoxide dismutase, and marker of lipid peroxidation, malondialdehyde (MDA), were assayed using standard procedures. The hematological profile, lipid profile, serum markers for kidney function and histopathological examination were also assessed.
Intoxication with RIF and INH markedly reduced the hematological indices and elevated the biochemical enzyme markers (AST, ALT and ALP, P < 0.001) and lipid profile (P < 0.001), while antioxidant biomarkers were significantly (P < 0.01) depressed and MDA was elevated. However, pretreatment with TOPE significantly (P < 0.001) alleviated this alteration and sustained the antioxidant potentials. The histopathological morphology supports the biochemical evidence of hepatoprotection.
Current study is indicative of potential antioxidant activity, hepatoprotective effects and plausible therapeutic alleviation of RIF-INH-induced hepatotoxicity of TOPE in laboratory animals.
药物性肝损伤会使抗结核药物治疗复杂化,是全球范围内导致死亡的主要原因。本研究旨在证实非洲吊灯果的果肉提取物对利福平(RIF)和异烟肼(INH)诱导的大鼠氧化应激的肝保护作用的民族医学主张。
通过用 RIF 和 INH(各 100mg/kg)口服灌胃 60d 诱导氧化应激性肝毒性模型,评价非洲吊灯果果肉提取物(TOPE)(125-500mg/kg)和水飞蓟素(50mg/kg)。评估丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)和碱性磷酸酶(ALP)等表明氧化应激和肝损伤的标志物。采用标准程序测定抗氧化状态的生物标志物,包括过氧化氢酶、谷胱甘肽还原酶、谷胱甘肽过氧化物酶和超氧化物歧化酶,以及脂质过氧化标志物丙二醛(MDA)。还评估了血液学特征、脂质谱、血清肾功能标志物和组织病理学检查。
用 RIF 和 INH 灌胃,使血液学指标显著降低,并使生化酶标志物(AST、ALT 和 ALP,P<0.001)和脂质谱(P<0.001)升高,而抗氧化生物标志物显著(P<0.01)降低,MDA 升高。然而,TOPE 预处理显著(P<0.001)减轻了这种变化,维持了抗氧化潜力。组织病理学形态支持了生化证据的肝保护作用。
本研究表明,TOPE 具有潜在的抗氧化活性、肝保护作用,并可能缓解 RIF-INH 诱导的实验动物肝毒性。