Boateng Anthony O, Patel Vinood B, Bligh S W Annie
School of Science, Faculty of Engineering & Science, University of Greenwich, Central Avenue, Chatham, Kent ME4 4TB, UK.
School of Life Science, College of Liberal Arts and Science, University of Westminster, 115 New Cavendish Street, London W1W 6UW, UK.
Biomolecules. 2025 May 16;15(5):726. doi: 10.3390/biom15050726.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is a metabolic disease characterised by the accumulation of fat in the liver. It is estimated that 30-38% of the world's adult population have MASLD, making it the most prevalent global chronic liver disease. Due to a lack of a therapy for MASLD, treatment has been mainly focussed on managing the conditions associated with the disease such as obesity, diabetes mellitus, and hyperlipidaemia. This study aimed to investigate the role played by phytochemicals including the following: gentiopicroside, sweroside, and swertiamarin, in promoting hepatocyte protection against the cytotoxic effects of fatty acids. species such as lutea, macrophylla, rigescens, and scabra are known to protect and enhance hepatocyte viability via their antioxidant, anti-inflammatory, and bitter components including the following: amarogentin gentianine, iso-orientin, swertiamarin, gentiopicroside, and sweroside. In this study, HepG2 cells pre-treated with phytochemicals gentiopicroside, sweroside, swertiamarin, and silymarin followed by an exposure to arachidonic acid (10, 30, 50 and 80 µM) were assessed for cell viability via MTT, mitochondrial function via seahorse assay, ROS levels via DCF assay, and annexin V-FITC for apoptosis. THLE-2 cells were also assayed for validation. The phytochemicals tested improved ATP production notably gentiopicroside, which improved ATP production by over 60% compared to untreated hepatocytes. Significant hepatocyte protection against lipotoxicity leading to apoptosis was also observed in gentiopicroside in the presence of 30 µM arachidonic acid with apoptosis reduced by over 50%. ROS production was reduced up to 60% by the pre-treatment of HepG2 cells with 20 µM, gentiopicroside, sweroside, swertiamarin, and silymarin, with the highest reduction observed in swertiamarin. It was concluded that phytochemicals gentiopicroside, sweroside, and swertiamarin play key roles in the hepatocyte protection against the cytotoxic effects of fatty acids. This protection is conferred by enhancing mitochondrial function in terms of increasing the maximal respiratory capacity in response to a high influx of fatty acids, promoting ATP production as well as scavenging ROS produced as a result of high fatty acid influx and increased mitochondrial respiration. Highlights: Gentiopicroside may minimise lipotoxicity leading to apoptosis and necrosis in hepatocytes in the presence of arachidonic acid. A pre-treatment of hepatocytes with phytochemicals, namely gentiopicroside, sweroside, and silymarin provides a degree of protection which may be attributed to the enhancement of mitochondrial function. Sweroside, silymarin, and swertiamarin may protect HepG2 and THLE-2 cells by scavenging ROS produced by arachidonic acid and the mitochondrial electron transport chain.
代谢功能障碍相关脂肪性肝病(MASLD)是一种以肝脏脂肪堆积为特征的代谢性疾病。据估计,全球30%-38%的成年人口患有MASLD,使其成为全球最普遍的慢性肝病。由于缺乏针对MASLD的治疗方法,治疗主要集中在管理与该疾病相关的病症,如肥胖、糖尿病和高脂血症。本研究旨在调查包括以下成分的植物化学物质:龙胆苦苷、獐牙菜苷和獐牙菜苦素,在促进肝细胞抵抗脂肪酸细胞毒性作用方面所起的作用。已知如淡黄、大叶、坚龙胆和糙叶龙胆等物种通过其抗氧化、抗炎和苦味成分(包括以下成分:苦味质、龙胆宁碱、异荭草素、獐牙菜苦素、龙胆苦苷和獐牙菜苷)来保护和提高肝细胞活力。在本研究中,用植物化学物质龙胆苦苷、獐牙菜苷、獐牙菜苦素和水飞蓟宾预处理HepG2细胞,然后暴露于花生四烯酸(分别为10、30、50和80 μM),通过MTT法评估细胞活力,通过海马分析评估线粒体功能,通过DCF分析评估ROS水平,并通过膜联蛋白V-FITC检测凋亡情况。还对THLE-2细胞进行检测以作验证。所测试的植物化学物质显著改善了ATP生成,尤其是龙胆苦苷,与未处理的肝细胞相比,其ATP生成提高了60%以上。在存在30 μM花生四烯酸的情况下,龙胆苦苷对导致凋亡的脂毒性也有显著的肝细胞保护作用,凋亡减少了50%以上。用20 μM龙胆苦苷、獐牙菜苷、獐牙菜苦素和水飞蓟宾预处理HepG2细胞可使ROS生成减少多达60%,其中獐牙菜苦素的减少幅度最大。得出的结论是,植物化学物质龙胆苦苷、獐牙菜苷和獐牙菜苦素在肝细胞抵抗脂肪酸细胞毒性作用中起关键作用。这种保护作用是通过增强线粒体功能实现的,即增加对大量脂肪酸流入的最大呼吸能力,促进ATP生成,并清除因大量脂肪酸流入和线粒体呼吸增加而产生的ROS。要点:在存在花生四烯酸的情况下,龙胆苦苷可能使肝细胞中导致凋亡和坏死的脂毒性降至最低。用植物化学物质,即龙胆苦苷、獐牙菜苷和水飞蓟宾对肝细胞进行预处理可提供一定程度的保护,这可能归因于线粒体功能的增强。獐牙菜苷、水飞蓟宾和獐牙菜苦素可能通过清除花生四烯酸和线粒体电子传递链产生的ROS来保护HepG2和THLE-2细胞。