Department of Medicinal Chemistry and Center for Natural Products, Drug Discovery and Development (CNPD3), University of Florida, Gainesville, FL 32610, USA.
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait.
Mar Drugs. 2023 Oct 25;21(11):553. doi: 10.3390/md21110553.
The monounsaturated fatty acid 7()-9-keto-hexadec-7-enoic acid () and three structurally related analogues with different oxidation states and degrees of unsaturation (-) were discovered from a marine benthic cyanobacterial mat collected from Delta Shoal, Florida Keys. Their structures were elucidated using NMR spectroscopy and mass spectrometry. The structure of contained an α,-unsaturated carbonyl system, a key motif required for the activation of the Keap1/Nrf2-ARE pathway that is involved in the activation of antioxidant and phase II detoxification enzymes. Compounds - were screened in ARE-luciferase reporter gene assay using stably transfected HEK293 cells, and only significantly induced Nrf2 activity at 32 and 10 µM, whereas - were inactive. As there is crosstalk between inflammation and oxidative stress, subsequent biological studies were focused on to investigate its anti-inflammatory potential. Compound induced , a well-known target gene of Nrf2, and suppressed transcript levels, which translated into reduced levels of nitric oxide in LPS-activated mouse macrophage RAW264.7 cells, a more relevant model for inflammation. RNA sequencing was performed to capture the effects of on a global level and identified additional canonical pathways and upstream regulators involved in inflammation and immune response, particularly those related to multiple sclerosis. A targeted survey of marine cyanobacterial samples from other geographic locations, including Guam, suggested the widespread occurrence of . Furthermore, the previous isolation of from marine diatoms and green algae implied a potentially important ecological role across marine algal eukaryotes and prokaryotes. The previous isolation from sea lettuce raises the possibility of dietary intervention to attenuate inflammation and related disease progression.
从佛罗里达群岛三角洲浅滩采集的海洋底栖蓝藻垫中发现了单不饱和脂肪酸 7()-9-酮-十六-7-烯酸 () 和三种结构相关的类似物,它们具有不同的氧化态和不饱和程度 (-)。使用 NMR 光谱和质谱法阐明了它们的结构。包含一个 α,β-不饱和羰基系统,这是激活 Keap1/Nrf2-ARE 途径的关键基序,该途径参与抗氧化和 II 相解毒酶的激活。使用稳定转染的 HEK293 细胞在 ARE-荧光素酶报告基因测定中筛选了 -,只有在 32 和 10 μM 时显著诱导 Nrf2 活性,而 - 则没有活性。由于炎症和氧化应激之间存在交叉对话,随后的生物学研究集中在 上,以研究其抗炎潜力。化合物 诱导 Nrf2 的靶基因 ,并抑制 转录水平,这导致 LPS 激活的小鼠巨噬细胞 RAW264.7 细胞中一氧化氮水平降低,这是更相关的炎症模型。进行了 RNA 测序以在全局水平上捕获 对的影响,并确定了涉及炎症和免疫反应的其他规范途径和上游调节剂,特别是与多发性硬化症相关的途径和调节剂。对包括关岛在内的其他地理位置的海洋蓝藻样本进行了靶向调查,表明 广泛存在。此外,先前从海洋硅藻和绿藻中分离出 暗示了其在海洋藻类真核生物和原核生物中具有潜在重要的生态作用。先前从海生菜中分离出来的 提出了通过饮食干预来减轻炎症和相关疾病进展的可能性。