Graduate Program in Pharmaceutical Sciences, Federal University of Espirito Santo - UFES, Avenida Marechal Campos 1468, 29047-105 Vitória, ES, Brazil.
Graduate Program in Pharmaceutical Sciences, Federal University of Espirito Santo - UFES, Avenida Marechal Campos 1468, 29047-105 Vitória, ES, Brazil; Department of Pharmaceutical Sciences, Federal University of Espirito Santo - UFES, Avenida Marechal Campos 1468, 29047-105 Vitória, ES, Brazil.
Biomed Pharmacother. 2018 Nov;107:1160-1165. doi: 10.1016/j.biopha.2018.08.098. Epub 2018 Aug 28.
The naphthopyranones paepalantine and 5-methoxy-3,4-dehydroxanthomegnin isolated from Paepalanthus sp, showed in previous studies antioxidant, anti-inflammatory, antitumour and antimicrobial potential, such as anti-Helicobacter pylori activity. H. pylori infection is one of the main causes of gastric cancer, causing an excessive inflammatory response through the neutrophils and macrophages infiltration, increasing the release of reactive species and thus inducing the production of pro-inflammatory mediators. In the present study, immunomodulatory activity of naphthopyranones in LPS-stimulated macrophages and cytotoxic action in gastric adenocarcinoma cell lines was evaluated. The potential of interaction of these substances in the iNOS binding site was investigated by molecular docking. Cytotoxic activity in gastric adenocarcinoma cells (AGS) was evaluated by the MTT assay. The results evidenced immunomodulatory potential by inhibiting the pro-inflammatory cytokines and nitric oxide produced by LPS-stimulated macrophages. Cytotoxic activity in AGS cell line was also reported. The results indicated that the studied naphthopyranones are viable alternatives in the treatment and prevention of H. pylori infection as well as the diseases related to this infection, especially gastric cancer.
从 Paepalanthus 属植物中分离得到的萘并吡喃酮 Paepalantine 和 5-甲氧基-3,4-脱氢黄烷镁,在先前的研究中显示出抗氧化、抗炎、抗肿瘤和抗菌等潜在作用,如抗幽门螺杆菌活性。幽门螺杆菌感染是胃癌的主要原因之一,它通过中性粒细胞和巨噬细胞浸润引起过度的炎症反应,增加活性物质的释放,从而诱导促炎介质的产生。在本研究中,评估了萘并吡喃酮对 LPS 刺激的巨噬细胞的免疫调节活性和对胃腺癌细胞系的细胞毒性作用。通过分子对接研究了这些物质在 iNOS 结合位点相互作用的潜力。通过 MTT 测定评估了这些物质对胃腺癌细胞(AGS)的细胞毒性作用。结果表明,这些萘并吡喃酮通过抑制 LPS 刺激的巨噬细胞产生的促炎细胞因子和一氧化氮,具有免疫调节潜力。对 AGS 细胞系的细胞毒性作用也进行了报道。结果表明,所研究的萘并吡喃酮是治疗和预防幽门螺杆菌感染以及与该感染相关疾病(尤其是胃癌)的可行选择。