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香叶基化和法呢基化类黄酮增加了小鼠巨噬细胞内活性氧的产生,但抑制了炎症反应。

Prenylated and geranylated flavonoids increase production of reactive oxygen species in mouse macrophages but inhibit the inflammatory response.

机构信息

Department of Natural Drugs, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences Brno , Palackého tř. 1/3, CZ 612 42, Brno, Czech Republic.

出版信息

J Nat Prod. 2013 Sep 27;76(9):1586-91. doi: 10.1021/np400242e. Epub 2013 Aug 16.

Abstract

In this study, four prenylated and geranylated flavonoids, cudraflavone B (1), pomiferin (2), osajin (3), and diplacone (4), were tested for their antioxidant and anti-inflammatory effects and to identify any potential relationships between chemical structure and antioxidant or anti-inflammatory properties. The selected flavonoids were examined in cell-free models to prove their ability to scavenge superoxide radicals, hydrogen peroxide, and hypochlorous acid. Further, the ability of the flavonoids to influence the formation of reactive oxygen species in the murine macrophage cell line J774.A1 was tested in the presence and absence of lipopolysaccharide (LPS). The ability of flavonoids to inhibit LPS-induced IκB-α degradation and COX-2 expression was used as a model for the inflammatory response. The present results indicated that the antioxidant activity was dependent on the chemical structure, where the catechol moiety is especially crucial for this effect. The most potent antioxidant activities in cell-free models were observed for diplacone (4), whereas cudraflavone B (1) and osajin (3) showed a pro-oxidant effect in J774.A1 cells. All flavonoids tested were able to inhibit IκB-α degradation, but only diplacone (4) also down-regulated COX-2 expression.

摘要

在这项研究中,测试了四种被prenylated 和 geranylated 的类黄酮,即 cudraflavone B(1)、pomiferin(2)、osajin(3)和 diplacone(4),以评估它们的抗氧化和抗炎作用,并确定化学结构与抗氧化或抗炎特性之间的潜在关系。选择的类黄酮在无细胞模型中进行了测试,以证明它们清除超氧自由基、过氧化氢和次氯酸的能力。此外,还在存在和不存在脂多糖(LPS)的情况下,测试了类黄酮对小鼠巨噬细胞系 J774.A1 中活性氧物种形成的影响。类黄酮抑制 LPS 诱导的 IκB-α 降解和 COX-2 表达的能力被用作炎症反应的模型。目前的结果表明,抗氧化活性取决于化学结构,其中儿茶酚部分对这种效应尤为重要。在无细胞模型中观察到最强的抗氧化活性的是 diplacone(4),而 cudraflavone B(1)和 osajin(3)在 J774.A1 细胞中表现出促氧化作用。所有测试的类黄酮都能够抑制 IκB-α 的降解,但只有 diplacone(4)也能下调 COX-2 的表达。

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