Lillsunde Katja-Emilia, Festa Carmen, Adel Harshada, De Marino Simona, Lombardi Valter, Tilvi Supriya, Nawrot Dorota A, Zampella Angela, D'Souza Lisette, D'Auria Maria Valeria, Tammela Päivi
Centre for Drug Research, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, P.O. Box 56, University of Helsinki, Helsinki FI-00014, Finland.
Department of Pharmacy, University of Naples Federico II (USNF), Naples I-80131, Italy.
Mar Drugs. 2014 Jul 3;12(7):4045-68. doi: 10.3390/md12074045.
Marine organisms and their metabolites represent a unique source of potential pharmaceutical substances. In this study, we examined marine-derived substances for their bioactive properties in a cell-based Chikungunya virus (CHIKV) replicon model and for in vitro anti-inflammatory activity. In the screening of a marine sample library, crude extracts from the Indian soft coral, Sinularia kavarattiensis, showed promising activity against the CHIKV replicon. Bioassay-guided chemical fractionation of S. kavarattiensis resulted in the isolation of six known norcembranoids (1-6) and one new compound, named kavaranolide (7). The structures were elucidated on the basis of NMR and MS spectroscopic data. Compounds 1-3 and 5-7 were evaluated for their replicon-inhibiting potential in the CHIKV model by using a luminescence-based detection technique and live cell imaging. Compounds 1 and 2 showed moderate inhibition of the CHIKV replicon, but imaging studies also revealed cytotoxic properties. Moreover, the effects of the isolated compounds on primary microglial cells, an experimental model for neuroinflammation, were evaluated. Compound 2 was shown to modulate the immune response in microglial cells and to possess potential anti-inflammatory properties by dose-dependently reducing the release of pro- and anti-inflammatory cytokines.
海洋生物及其代谢产物是潜在药物物质的独特来源。在本研究中,我们在基于细胞的基孔肯雅病毒(CHIKV)复制子模型中检测了海洋来源物质的生物活性特性,并检测了其体外抗炎活性。在对海洋样本库的筛选中,来自印度软珊瑚卡瓦拉蒂软珊瑚(Sinularia kavarattiensis)的粗提物对CHIKV复制子显示出有前景的活性。对卡瓦拉蒂软珊瑚进行生物测定指导的化学分级分离,得到了六种已知的降碳环类化合物(1 - 6)和一种新化合物,命名为卡瓦拉诺内酯(7)。根据核磁共振(NMR)和质谱(MS)光谱数据阐明了其结构。通过基于发光的检测技术和活细胞成像,在CHIKV模型中评估了化合物1 - 3和5 - 7的复制子抑制潜力。化合物1和2对CHIKV复制子表现出适度抑制作用,但成像研究也揭示了其细胞毒性特性。此外,评估了分离出的化合物对原代小胶质细胞(一种神经炎症实验模型)的影响。化合物2被证明可调节小胶质细胞中的免疫反应,并通过剂量依赖性降低促炎和抗炎细胞因子的释放而具有潜在的抗炎特性。