In silico, in vitro: antioxidant and antihepatotoxic activity of gnetol from Gnetum ula Brongn

Preetham Jinadatta, Sharath Rajshekarappa, Kiran Sundera Raja Rao, Sujan Ganapathy Pasura Subbaiah, Sudhesh L Shastri
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引用次数: 7

Abstract

Introduction: Gnetum ula is a notable medicinal plant used to cure various ailments. The stem part of the plant is used traditionally to treat jaundice and other disorders. The present work is to investigate the in vitro hepatoprotective and antioxidant activity of ethanol extract of stem of G. ula (GUE) and its isolated compound gnetol. Methods: Column chromatography was carried out for GUE and various column fractions were obtained. DPPH and reducing power assays were performed for GUE and column fractions. The potent fraction was characterized, interpreted and tested for in vitro hepatoprotective activity on the BRL3A cell line. In silico docking studies of gnetol compound on the protein TGF-β (transforming growth factor – β) and Peroxisome proliferator-activated receptor α (PPARα) was carried out. Results: DPPH scavenging and reducing power assay showed that the fourth column fraction has antioxidant potential than other fractions. The fourth column fraction was characterized to obtain gnetol compound. BRL3A cell line was used for the toxicity study of GUE and gnetol. Both, the extract and the isolated compound were found to be nontoxic with CTC50 value more than 1000 µg/mL. At the concentration of 200 µg/mL, GUE and gnetol offered cell protection of 50.2% and 54.3%, however, silymarin showed 77.15% protection at 200 µg/mL concentration against CCl4 treated BRL3A cell line. The docking results of the ligand molecule TGF-β showed that gnetol has the binding affinity of -7.0 and standard silymarin being -6.8. TGF-β showed good hydrophobic interactions and formed two hydrogen bonds with the amino acids. For PPARα protein, gnetol showed the binding affinity of -8.4 and silymarin with -6.5. Hydrogen bonding and good hydrophobic interactions against the amino acid molecules in relation to the PPARα protein are shown. Conclusion: Gnetum ula stem extract and its isolated compound are safe and offered significant hepatoprotection against CCl4 induced toxicity. Isolated compound gnetol exhibited a potent antioxidant activity offering protection to liver damage. However, in vivo studies need to be carried out to validate the traditional use of G. ula .
体外实验:根草甘露醇的抗氧化和抗肝毒活性
木耳是一种著名的药用植物,用于治疗各种疾病。传统上,这种植物的茎部分被用来治疗黄疸和其他疾病。本研究旨在研究乌拉茎乙醇提取物(GUE)及其分离化合物gnetol的体外保肝和抗氧化活性。方法:采用柱层析法对GUE进行色谱分析,得到不同的柱馏分。DPPH和还原功率测定GUE和柱分数。对该有效组分进行了表征、解释并检测了其对BRL3A细胞系的体外肝保护活性。在硅对接研究中,糖醇化合物对TGF-β(转化生长因子-β)蛋白和过氧化物酶体增殖激活受体α (PPARα)的作用进行了研究。结果:四柱提取物对DPPH的清除和还原能力试验表明,四柱提取物具有较强的抗氧化能力。对第四柱馏分进行表征,得到糖醇类化合物。采用BRL3A细胞系进行GUE和gnetol的毒性研究。提取物和分离物均无毒,CTC50值均大于1000µg/mL。在200µg/mL浓度下,GUE和gnetol对CCl4处理的BRL3A细胞株的保护作用分别为50.2%和54.3%,而水飞蓟素在200µg/mL浓度下对CCl4处理的BRL3A细胞株的保护作用为77.15%。配体分子TGF-β的对接结果表明,糖醇的结合亲和力为-7.0,标准水飞蓟素的结合亲和力为-6.8。TGF-β表现出良好的疏水相互作用,与氨基酸形成两个氢键。对于PPARα蛋白,糖醇的结合亲和力为-8.4,水飞蓟素的结合亲和力为-6.5。显示了与PPARα蛋白相关的氨基酸分子的氢键和良好的疏水相互作用。结论:木耳提取物及其分离物是安全的,对CCl4毒性具有明显的肝保护作用。分离化合物糖醇具有抗氧化活性,对肝损伤具有保护作用。然而,需要进行体内研究来验证G. ula的传统使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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