Department of Pharmacognosy and Molecular Basis of Phytotherapy , Medical University of Warsaw , Warsaw 02-097 , Poland.
Institute of Pharmacy/Pharmacognosy and Center for Molecular Biosciences Innsbruck (CMBI) , University of Innsbruck , Innsbruck 6020 , Austria.
J Nat Prod. 2019 Feb 22;82(2):375-385. doi: 10.1021/acs.jnatprod.8b00939. Epub 2019 Jan 17.
During chronic inflammation, neutrophils acting locally as effector cells not only activate antibacterial defense but also promote the inflammatory response. Interleukin 8 (IL-8), the main cytokine produced by activated neutrophils, positively correlates with the severity of respiratory tract diseases. By screening European plants traditionally used for treating respiratory tract diseases, we found that extracts of aerial parts of Eupatorium cannabinum inhibit IL-8 release from neutrophils. Using bioassay-guided fractionation, we identified five sesquiterpene lactones, eupatoriopicrin (1), 5'-deoxyeupatoriopicrin (2), hiyodorilactone A (3), 3-hydroxy-5'- O-acetyleupatoriopicrin = hiyodorilactone D (4), and hiyodorilactone B (5), that efficiently (IC < 1 μM) inhibited IL-8 and TNF-α release in lipopolysaccharide (LPS)-stimulated human neutrophils. Moreover, all these sesquiterpene lactones suppressed the adhesion of human neutrophils to an endothelial monolayer by downregulating the expression of the β2 integrin CD11b/CD18 on the neutrophil surface. Furthermore, eupatoriopicrin efficiently suppressed LPS-induced phosphorylation of p38 MAPK and ERK and attenuated neutrophil infiltration in the thioglycolate-induced peritonitis model in mice. Altogether, these results demonstrate the potential of the sesquiterpene lactone eupatoriopicrin as a lead substance for targeting inflammation.
在慢性炎症中,作为效应细胞的中性粒细胞不仅激活抗菌防御机制,还促进炎症反应。白细胞介素 8(IL-8)是激活的中性粒细胞产生的主要细胞因子,与呼吸道疾病的严重程度呈正相关。通过筛选欧洲传统上用于治疗呼吸道疾病的植物,我们发现大麻叶泽兰地上部分的提取物可抑制中性粒细胞释放白细胞介素 8。通过生物测定指导的分步分离,我们鉴定出了五种倍半萜内酯,即泽兰苦内酯(1)、5'-去氧泽兰苦内酯(2)、hiydorilactone A(3)、3-羟基-5'-O-乙酰泽兰苦内酯=hiydorilactone D(4)和 hiydorilactone B(5),它们可有效(IC < 1 μM)抑制脂多糖(LPS)刺激的人中性粒细胞中白细胞介素 8 和肿瘤坏死因子-α的释放。此外,所有这些倍半萜内酯都通过下调中性粒细胞表面的β2 整合素 CD11b/CD18 的表达,抑制人中性粒细胞与内皮单层的黏附。此外,泽兰苦内酯可有效抑制 LPS 诱导的 p38 MAPK 和 ERK 的磷酸化,并减轻小鼠巯基醋酸盐诱导的腹膜炎模型中的中性粒细胞浸润。总之,这些结果表明倍半萜内酯泽兰苦内酯作为一种靶向炎症的潜在先导物质。