Anggreini Putri, Kuncoro Hadi, Sumiwi Sri Adi, Levita Jutti
Faculty of Pharmacy, Padjadjaran University, Sumedang, 46363, Indonesia.
Faculty of Pharmacy, Mulawarman University, Samarinda, 75119, Indonesia.
J Exp Pharmacol. 2023 Dec 22;15:513-527. doi: 10.2147/JEP.S438435. eCollection 2023.
is a fern plant with various pharmacological activities, and phytosterols were reported contained in the n-hexane and ethyl acetate extract of this plant. Phytosterols are known to inhibit steatosis, oxidative stress, and inflammation. Sirtuin 1 (SIRT1) and adenosine monophosphate-activated protein kinase (AMPK) are the key proteins that control lipogenesis. However, information about on SIRT1 and AMPK is still lacking.
This study aims to investigate the binding mode of phytosterols in extract towards AMPK and SIRT1, and the toxicity of the extract against brine shrimp () larvae, and to determine the phenols and sterols levels in the extract.
The molecular docking was performed towards SIRT1 and AMPK using AutoDock v4.2.6, the toxicity of the extract was assayed against brine shrimp () larvae, and the phytosterols were analyzed by employing a thin layer chromatography densitometry, and the total phenols were by spectrophotometry.
The molecular docking study revealed that β-sitosterol and stigmasterol could occupy the active allosteric-binding site of SIRT1 and AMPK by binding to important residues similar to the protein's activators. The cold extraction of the plant yields 15.86% w/w. Phytochemical screening revealed the presence of phenols, steroids, flavonoids, alkaloids, and saponins. The total phenols are equivalent to 126 mg gallic acid (GAE)/g dry extract, the total sterols are 954.04 µg/g, and the β-sitosterol level is 283.55 µg/g. The LC value of the extract towards larvae is 203.704 ppm.
extract may have the potential to be further explored for its pharmacology activities, particularly in the discovery of plant-based anti-dyslipidemic drug candidates. However, further studies are needed to confirm their roles in alleviating lipid disorders.
[植物名称]是一种具有多种药理活性的蕨类植物,据报道该植物的正己烷和乙酸乙酯提取物中含有植物甾醇。已知植物甾醇可抑制脂肪变性、氧化应激和炎症。沉默调节蛋白1(SIRT1)和腺苷单磷酸活化蛋白激酶(AMPK)是控制脂肪生成的关键蛋白。然而,关于[植物名称]中SIRT1和AMPK的信息仍然缺乏。
本研究旨在研究[植物名称]提取物中植物甾醇与AMPK和SIRT1的结合模式,以及该提取物对卤虫幼虫的毒性,并测定提取物中的酚类和甾醇含量。
使用AutoDock v4.2.6对SIRT1和AMPK进行分子对接,测定提取物对卤虫幼虫的毒性,采用薄层色谱密度法分析植物甾醇,用分光光度法测定总酚含量。
分子对接研究表明,β-谷甾醇和豆甾醇可通过与类似于蛋白质激活剂的重要残基结合,占据SIRT1和AMPK的活性变构结合位点。该植物的冷提取物得率为15.86% w/w。植物化学筛选显示存在酚类、甾体、黄酮类、生物碱和皂苷。总酚相当于126 mg没食子酸(GAE)/g干提取物,总甾醇为954.04 µg/g,β-谷甾醇含量为283.55 µg/g。提取物对卤虫幼虫的LC值为203.704 ppm。
[植物名称]提取物可能有进一步探索其药理活性的潜力,特别是在发现基于植物的抗血脂异常候选药物方面。然而,需要进一步研究来证实它们在缓解脂质紊乱中的作用。