Department of Biological Sciences, Al-Hikmah University, Ilorin, Nigeria.
Antioxidants, Redox Biology and Toxicology Research Laboratory, Department of Medical Biochemistry, College of Health Sciences, Nile University of Nigeria, Abuja, Nigeria.
Drug Chem Toxicol. 2020 Nov;43(6):567-573. doi: 10.1080/01480545.2018.1523187. Epub 2018 Dec 26.
Menadione (Vitamin K) is an over-the-counter (OTC) drug used in the treatment of abdominal cramps, colitis, diarrhea, hay fever, hemorrahage, hypoprothrombinemia, and joint pains. In this study, we evaluated the protective influence of protocatechuic acid on menadione-induced hepatotoxicity in rats. Rats were randomized into five groups (A-E) of five rats each. Control rats orally received 1% dimethyl sulfoxide (DMSO) in distilled water (the vehicle for protocatechuic administration) for 7 days. In addition, control rats intraperioneally received olive oil (vehicle for menadione administration) on the 7th day. Groups B, D, and E received single dose of 100 mg/kg body weight menadione on day 7. Furthermore, groups C-E were pretreated with protocatechuic acid for 7 days. Pretreatment of rats with protocatechuic acid significantly halted menadione mediated-alterations in serum alkaline phosphatase, alanine and aspartate aminotransferases, albumin, and total bilirubin. Furthermore, menadione-mediated increase in superoxide ion and hydrogen peroxide with concomitant decrease in the activities of superoxide dismutase and catalase were significantly reversed by protocatechuic acid. Protocatechuic acid annulled menadione-mediated decrease in glutathione S-transferase and NADH: quinone oxidoreductase-1 through nuclear erythroid related factor-2 (Nrf-2). In addition, the decreased glutathione and increased glutathione disulfide, caspase-3, fragmented DNA, malondialdehyde and protein carbonyl were reversed. Results of this study show that protocatechuic acid protects against menadione-induced oxidative stress in rats by enhancing the antioxidant and phase II enzymes through Nrf-2.
甲萘醌(维生素 K)是一种非处方(OTC)药物,用于治疗腹痛、结肠炎、腹泻、花粉热、出血、低凝血酶原血症和关节疼痛。在这项研究中,我们评估了原儿茶酸对大鼠甲萘醌诱导的肝毒性的保护作用。大鼠随机分为五组(A-E),每组 5 只。对照组大鼠口服 1%二甲基亚砜(DMSO)在蒸馏水中(原儿茶酸给药的载体)7 天。此外,对照组大鼠在第 7 天腹膜内注射橄榄油(甲萘醌给药的载体)。第 7 天,B、D 和 E 组大鼠给予 100mg/kg 体重的甲萘醌单剂量。此外,C-E 组大鼠用原儿茶酸预处理 7 天。用原儿茶酸预处理大鼠可显著阻止甲萘醌介导的血清碱性磷酸酶、丙氨酸和天冬氨酸转氨酶、白蛋白和总胆红素的变化。此外,原儿茶酸显著逆转了甲萘醌介导的超氧阴离子和过氧化氢的增加,以及超氧化物歧化酶和过氧化氢酶活性的降低。原儿茶酸通过核红细胞相关因子 2(Nrf-2)消除了甲萘醌介导的谷胱甘肽 S-转移酶和 NADH:醌氧化还原酶-1 的减少。此外,还逆转了谷胱甘肽的减少和谷胱甘肽二硫化物、半胱天冬酶-3、片段化 DNA、丙二醛和蛋白质羰基的增加。这项研究的结果表明,原儿茶酸通过增强抗氧化和 II 相酶通过 Nrf-2 来保护大鼠免受甲萘醌诱导的氧化应激。