Campili Mendes, Jéssica Raquel Borges Monteiro, Rodrigo de Almeida Romagna, Aliny Rodrigues de Jesus da Conceição, Pedro Henrique Tregnano, Amanda Eiriz Feu, Rita de Cássia Ribeiro Gonçalves, Warley de Souza Borges, Ricardo Machado Kuster, Rodrigo Rezende Kitagawa
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引用次数: 0
Abstract
Medicinal plants and their phytocompounds are valuable shortcuts for discovering new, safer biologically active compounds or herbal medicines with reduced adverse effects. In this study, medicinal plant species were initially selected from Brazilian traditional medicine using database from in silico and in vitro studies. Virtual screening study was carried out with a phytochemical database previously reported in the literature. The biological activity was evaluated in silico by PASS Online and molecular docking, then validated by in vitro anti-Helicobacter pylori assay. The chemical profile of the species was obtained by ESI(±)FT-ICR MS and LC-MS-DAD analysis. Vernonia condensata, Bauhinia forficata, Jatropha gossypiifolia, and Sonalum paniculatum were selected based on a survey of the literature for use of gastric diseases and anti-Helicobacter pylori potential. After PASS analysis, Jatropha gossypiifolia was selected for in vitro study because its compounds showed anti-H. pylori activity potential, inhibiting fumarate reductase enzyme. J. gossypiifolia extracted showed MIC of 64 µg/mL and MBC of 128 µg/mL in the in vitro anti-H. pylori assay. ESI(±)FT-ICR MS and LC-MS-DAD analysis showed compounds as luteolin (1: ), isovitexin (2: ), luteolin-7-O-glucoside (3: ), isoorientin (4: ), and 3-genistein-8-C-glucoside (5: ). Molecular docking analysis showed a potential interaction of compounds in the enzyme active site such as hydrogen bonds with Arg404 and a similar interaction to fumaric acid, except for isoorientin (3: ). J. gossypiifolia showed promising activity and may represent a future alternative to treat H. pylori infections and their deleterious effects, reinforcing the therapeutic potential of this plant.
药用植物及其植物化合物是发现新的、更安全的生物活性化合物或副作用更小的草药的宝贵捷径。在这项研究中,药用植物物种最初从巴西传统医学中通过计算机和体外研究数据库选择。虚拟筛选研究是利用文献中先前报道的植物化学数据库进行的。通过PASS Online和分子对接对其生物活性进行了计算机评价,并通过体外抗幽门螺杆菌实验对其进行了验证。通过ESI(±)FT-ICR MS和LC-MS-DAD分析获得了该物种的化学特征。在查阅文献的基础上,筛选出水杨、紫荆花、麻疯树和细叶索纳姆,研究其在胃病中的应用和抗幽门螺杆菌的潜力。通过PASS分析,选择麻疯树进行体外研究,因为其化合物具有抗h。幽门螺杆菌活性电位,抑制富马酸还原酶。棉叶提取物抗h的MIC为64µg/mL, MBC为128µg/mL。螺杆菌化验。ESI(±)FT-ICR MS和LC-MS-DAD分析显示化合物为木犀草素(1∶)、异牡荆素(2∶)、木犀草素-7- o -葡萄糖苷(3∶)、异荭草苷(4∶)和3-染料木素-8- c -葡萄糖苷(5∶)。分子对接分析显示,除了异荭草苷外,该酶活性位点上的化合物可能与Arg404存在氢键等相互作用,与富马酸也存在类似的相互作用(3:)。棉叶棉显示出良好的活性,可能是治疗幽门螺杆菌感染及其有害影响的未来选择,增强了该植物的治疗潜力。
期刊介绍:
Planta Medica is one of the leading international journals in the field of natural products – including marine organisms, fungi as well as micro-organisms – and medicinal plants. Planta Medica accepts original research papers, reviews, minireviews and perspectives from researchers worldwide. The journal publishes 18 issues per year.
The following areas of medicinal plants and natural product research are covered:
-Biological and Pharmacological Activities
-Natural Product Chemistry & Analytical Studies
-Pharmacokinetic Investigations
-Formulation and Delivery Systems of Natural Products.
The journal explicitly encourages the submission of chemically characterized extracts.