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Inhibition of COX-2 and PGE2 in LPS-stimulated RAW264.7 cells by lonimacranthoide VI a chlorogenic acid ester saponin

机译:一种绿原酸酯皂苷lonimantranthoide VI对LPS刺激的RAW264.7细胞中COX-2和PGE2的抑制作用

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摘要

Lonimacranthoide VI, first isolated from the flower buds of Lonicera macranthoides in our previous study, is a rare chlorogenic acid ester acylated at C-23 of hederagenin. In the present study, the anti-inflammatory effects of lonimacranthoide VI were studied. Lipopolysaccharides (LPS) induced an inflammatory response through the production of prostaglandin E2 (PGE2), and these levels were reduced when lonimacranthoide VI was pre-administered. Additionally, the mechanism of the anti-inflammatory effects of lonimacranthoide VI was investigated by measuring cyclooxygenase (COX) activity and mRNA expression. The results showed that lonimacranthoide VI inhibited mRNA expression and in vitro activity of COX-2 in a dose-dependent manner, whereas only the higher lonimacranthoide VI concentration possibly reduced COX-1 expression and in vitro activity. Taken together, these results indicate that lonimacranthoide VI is an important anti-inflammatory constituent of Lonicera macranthoides and that the anti-inflammatory effect is attributed to the inhibition of PGE2 production through COX activity and mRNA expression.
机译:Lonimacranthoide VI是我们以前的研究中首次从忍冬忍冬的花蕾中分离出来的,是一种稀有的绿豆酸酯,其在二十碳三烯生成素的C-23处被酰化。在本研究中,研究了lonimacranthoide VI的抗炎作用。脂多糖(LPS)通过产生前列腺素E2(PGE2)诱导炎症反应,当预先服用lonimantranthoide VI时,这些水平会降低。此外,通过测量环氧合酶(COX)活性和mRNA表达,研究了lonimantrantantide VI的抗炎作用机理。结果表明,im虫酰胺VI以剂量依赖的方式抑制COX-2的mRNA表达和体外活性,而只有较高的im虫VI浓度可能会降低COX-1的表达和体外活性。综上所述,这些结果表明lonimacranthoide VI是Lonicera macranthoides的重要抗炎成分,并且抗炎作用归因于通过COX活性和mRNA表达抑制PGE2的产生。

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