酒精引起的氧化应激是肝病发展的关键因素,草药替代品是改善肝毒性作用的重要手段。该研究旨在评估番荔枝(Artabotrys odoratissimus)的保肝潜力,这是番荔枝科的一种重要药用灌木。使用 RP-HPLC 检测树皮乙醇提取物 (BEE) 中的酚类化合物。通过细胞活力测定、线粒体膜电位 (MMP) 测定、活性氧 (ROS) 测定、双染测定和蛋白质印迹,研究了 HepG2 细胞对乙醇诱导损伤的体外保肝活性。体内小鼠模型用于通过肝功能酶、脂质谱和组织病理学评估酒精诱导的应激。用 HPLC 检测到的所有 13 种酚类化合物都与天冬氨酸氨基转移酶 (AST)、碱性磷酸酶 (ALP) 和诱导型一氧化氮合酶 (NO) 等蛋白质靶标对接。RP-HPLC 检测到各种酚类物质的存在,包括芦丁、绿原酸和儿茶素等。BEE 与乙醇的共同给药减轻了细胞死亡,与阴性对照相比,HepG2 细胞中的 ROS 和 MMP。该提取物还调节了 MAP 激酶/caspase-3 通路,从而在 HepG2 细胞中显示出保护作用。此外,在单次中毒剂量(5 克/千克体重)之前,用提取物对小鼠模型进行 14 天的预处理,通过使肝功能酶、脂质谱和胆红素水平接近正常来减少肝损伤。计算机分析表明,芦丁与研究中的所有目标蛋白都表现出最佳的结合亲和力。这些结果证明 BEE 在肝细胞和体内模型中对乙醇诱导的氧化应激具有显着的保肝作用,并通过计算机分析进一步验证了这一点。从而显示出对 HepG2 细胞的保护作用。此外,在单次中毒剂量(5 克/千克体重)之前,用提取物对小鼠模型进行 14 天的预处理,通过使肝功能酶、脂质谱和胆红素水平接近正常来减少肝损伤。计算机分析表明,芦丁与研究中的所有目标蛋白都表现出最佳的结合亲和力。这些结果证明 BEE 在肝细胞和体内模型中对乙醇诱导的氧化应激具有显着的保肝作用,并通过计算机分析进一步验证了这一点。从而显示出对 HepG2 细胞的保护作用。此外,在单次中毒剂量(5 克/千克体重)之前,用提取物对小鼠模型进行 14 天的预处理,通过使肝功能酶、脂质谱和胆红素水平接近正常来减少肝损伤。计算机分析表明,芦丁与研究中的所有目标蛋白都表现出最佳的结合亲和力。这些结果证明 BEE 在肝细胞和体内模型中对乙醇诱导的氧化应激具有显着的保肝作用,并通过计算机分析进一步验证了这一点。血脂和胆红素接近正常。计算机分析表明,芦丁与研究中的所有目标蛋白都表现出最佳的结合亲和力。这些结果证明 BEE 在肝细胞和体内模型中对乙醇诱导的氧化应激具有显着的保肝作用,并通过计算机分析进一步验证了这一点。血脂和胆红素接近正常。计算机分析表明,芦丁与研究中的所有目标蛋白都表现出最佳的结合亲和力。这些结果证明 BEE 在肝细胞和体内模型中对乙醇诱导的氧化应激具有显着的保肝作用,并通过计算机分析进一步验证了这一点。
"点击查看英文标题和摘要"
Artabotrys odoratissimus Bark Extract Restores Ethanol Induced Redox Imbalance and Toxicity in Hepatocytes and In Vivo Model
Alcohol-induced oxidative stress is a key player in the development of liver diseases, and herbal alternatives are important means of ameliorating the hepatotoxic effects. The study aimed to evaluate the hepatoprotective potentiality of Artabotrys odoratissimus, an important medicinal shrub from the family Annonaceae. The phenolic compounds from bark ethanol extract (BEE) were detected using RP-HPLC. The in vitro hepatoprotective activity against ethanol-induced damage was studied in HepG2 cells with cell viability assays, mitochondrial membrane potential (MMP) assay, reactive oxygen species (ROS) assay, double staining assay and western blotting. The in vivo mice model was used to evaluate the alcohol-induced stress with liver function enzymes, lipid profile and histopathology. All the thirteen phenolic compounds detected with HPLC were docked onto protein targets such as aspartate amino transferase (AST), alkaline phosphatase (ALP) and inducible nitric oxide synthase (NO). The RP-HPLC detected the presence of various phenolics including rutin, chlorogenic acid and catechin, amongst others. Co-administration of BEE with ethanol alleviated cell death, ROS and MMP in HepG2 cells compared to the negative control. The extract also modulated the MAP kinase/caspase-3 pathway, thereby showing protective effects in HepG2 cells. Also, pre-treatment for 14 days with the extract in the mice model before a single toxic dose (5 g/kg body weight) reduced the liver injury by bringing the levels of liver function enzymes, lipid profile and bilirubin to near normal. In silico analysis revealed that rutin showed the best binding affinity with all the target proteins in the study. These results provide evidence that BEE possesses significant hepatoprotective effects against ethanol-induced oxidative stress in hepatic cells and in vivo models, which is further validated with in silico analysis.