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Anti-Inflammatory Activity Comparison among Scropoliosides—Catalpol Derivatives with 6-O-Substituted Cinnamyl Moieties

机译:Scropoliosides-具有6-O取代肉桂基部分的Catalpol衍生物之间的抗炎活性比较

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摘要

We have previously shown that scropolioside B has higher anti-inflammatory activity than catalpol does after the inhibition of nuclear factor (NF)-κB activity and IL-1β expression, maturation, and secretion. Various scropoliosides were extracted, isolated, and purified from Scrophularia dentata Royle ex Benth. We then compared their anti-inflammatory activities against LPS-induced NF-κB activity, cytokines mRNA expression, IL-1β secretion, and cyclooxygenase-2 activity. The inhibitory effects of the scropoliosides varied depending on whether the 6-O-substituted cinnamyl moiety was linked to C′′ 2-OH, C′′3-OH, or C′′4-OH, and on the number of moieties linked, which is closely related to the enhancement of antiinflammatory activity. Among these compounds, scropolioside B had the strongest antiinflammatory effects.
机译:先前我们已经显示,在抑制核因子(NF)-κB活性以及IL-1β表达,成熟和分泌后,scropolioside B具有比catalpol更高的抗炎活性。从Benth的齿状玄参Royle中提取,分离和纯化多种玄参苷。然后,我们比较了它们对LPS诱导的NF-κB活性,细胞因子mRNA表达,IL-1β分泌和环氧合酶2活性的抗炎活性。 scropoliosides的抑制作用取决于6-O-取代的肉桂基部分是连接到C''2-OH,C''3-OH还是C''4-OH以及连接的部分数而变化,这与抗炎活性的增强密切相关。在这些化合物中,scropolioside B具有最强的抗炎作用。

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