UNCW Center for Marine Science, 5600 Marvin K Moss Lane, Wilmington, NC 28409, USA.
Mar Drugs. 2019 Mar 20;17(3):184. doi: 10.3390/md17030184.
Chronic respiratory diseases, including chronic obstructive pulmonary disease (COPD), cystic fibrosis, and asthma, are some of the leading causes of illness and fatalities worldwide. The search for novel treatments led to the exploration of marine natural products as drug candidates to combat the debilitating effects of mucus accumulation and chronic inflammation. Previous research showed that an alga-derived compound, brevenal, could attenuate the effects of inflammatory agents, but the mechanisms by which it exerted its effects remained unclear. We investigated the effects of brevenal on lipopolysaccharide (LPS) induced cytokine/chemokine production from murine macrophages and human lung epithelial cells. It was found that brevenal reduces proinflammatory mediator secretion while preserving anti-inflammatory secretion from these cells. Furthermore, we found that brevenal does not alter cell surface Toll-like receptor 4 (TLR4) expression, thereby maintaining the cells' ability to respond to bacterial infection. However, brevenal does alter macrophage activation states, as demonstrated by reduced expression of both M1 and M2 phenotype markers, indicating this putative anti-inflammatory drug shifts innate immune cells to a less active state. Such a mechanism of action would be ideal for reducing inflammation in the lung, especially with patients suffering from chronic respiratory diseases, where inflammation can be lethal.
慢性呼吸系统疾病,包括慢性阻塞性肺疾病(COPD)、囊性纤维化和哮喘,是全球导致疾病和死亡的主要原因之一。为了寻找新的治疗方法,人们开始探索海洋天然产物作为药物候选物,以对抗黏液积聚和慢性炎症的破坏性影响。先前的研究表明,一种来源于藻类的化合物——brevenal 可以减轻炎症介质的作用,但它发挥作用的机制尚不清楚。我们研究了 brevenal 对脂多糖(LPS)诱导的小鼠巨噬细胞和人肺上皮细胞细胞因子/趋化因子产生的影响。结果发现,brevenal 可减少促炎介质的分泌,同时保留这些细胞的抗炎分泌。此外,我们发现 brevenal 不会改变细胞表面 Toll 样受体 4(TLR4)的表达,从而维持细胞对细菌感染的反应能力。然而,brevenal 确实改变了巨噬细胞的激活状态,表现为 M1 和 M2 表型标志物的表达均降低,这表明这种潜在的抗炎药物将先天免疫细胞转变为一种不那么活跃的状态。这种作用机制对于减轻肺部炎症非常理想,特别是对于患有慢性呼吸系统疾病的患者,因为炎症可能是致命的。