Faculty of Pharmaceutical Sciences, University of Iceland, Hofsvallagata 53, 107 Reykjavik, Iceland.
Interdisciplinary Centre of Marine and Environmental Research (CIIMAR/CIMAR), University of Porto, Avenida General Norton de Matos, s/n, 4450-208 Matosinhos, Portugal.
Mar Drugs. 2019 May 10;17(5):280. doi: 10.3390/md17050280.
Obesity is a complex disease resulting in several metabolic co-morbidities and is increasing at epidemic rates. The marine environment is an interesting resource of novel compounds and in particular cyanobacteria are well known for their capacity to produce novel secondary metabolites. In this work, we explored the potential of cyanobacteria for the production of compounds with relevant activities towards metabolic diseases using a blend of target-based, phenotypic and zebrafish assays as whole small animal models. A total of 46 cyanobacterial strains were grown and biomass fractionated, yielding in total 263 fractions. Bioactivities related to metabolic function were tested in different and models. Studying adipogenic and thermogenic gene expression in brown adipocytes, lipid metabolism and glucose uptake in hepatocytes, as well as lipid metabolism in zebrafish larvae, we identified 66 (25%) active fractions. This together with metabolite profiling and the evaluation of toxicity allowed the identification of 18 (7%) fractions with promising bioactivity towards different aspects of metabolic disease. Among those, we identified several known compounds, such as eryloside T, leptosin F, pheophorbide A, phaeophytin A, chlorophyll A, present as minor peaks. Those compounds were previously not described to have bioactivities in metabolic regulation, and both known or unknown compounds could be responsible for such effects. In summary, we find that cyanobacteria hold a huge repertoire of molecules with specific bioactivities towards metabolic diseases, which needs to be explored in the future.
肥胖是一种复杂的疾病,会导致多种代谢合并症,并以流行的速度增加。海洋环境是一种有趣的新型化合物资源,特别是蓝藻以其产生新型次生代谢物的能力而闻名。在这项工作中,我们使用基于目标、表型和斑马鱼的组合测定法作为整体小动物模型,探索了蓝藻生产对代谢性疾病具有相关活性的化合物的潜力。总共培养了 46 株蓝藻菌株并进行了生物质分级,共得到 263 个级分。在不同的 和 模型中测试了与代谢功能相关的生物活性。研究棕色脂肪细胞中的脂肪生成和生热基因表达、肝细胞中的脂质代谢和葡萄糖摄取,以及斑马鱼幼虫中的脂质代谢,我们鉴定出 66 个(25%)有活性的级分。这与代谢物分析和毒性评估相结合,确定了 18 个(7%)具有针对代谢性疾病不同方面有前景的生物活性的级分。其中,我们鉴定出了几种已知的化合物,如 eryloside T、leptosin F、pheophorbide A、phaeophytin A、叶绿素 A,它们以微量峰的形式存在。这些化合物以前没有被描述为具有代谢调节中的生物活性,而无论是已知的还是未知的化合物都可能对此类作用负责。总之,我们发现蓝藻拥有大量针对代谢性疾病的具有特定生物活性的分子,这在未来需要进一步探索。