首页> 外文期刊>Biochemical Pharmacology >Wogonin, baicalin, and baicalein inhibition of inducible nitric oxide synthase and cyclooxygenase-2 gene expressions induced by nitric oxide synthase inhibitors and lipopolysaccharide.
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Wogonin, baicalin, and baicalein inhibition of inducible nitric oxide synthase and cyclooxygenase-2 gene expressions induced by nitric oxide synthase inhibitors and lipopolysaccharide.

机译:Wogonin,黄ical苷和黄ical苷对一氧化氮合酶抑制剂和脂多糖诱导的可诱导型一氧化氮合酶和环氧合酶-2基因表达的抑制作用。

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摘要

We previously reported that oroxylin A, a polyphenolic compound, was a potent inhibitor of lipopolysaccharide (LPS)-induced expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). In the present study, three oroxylin A structurally related polyphenols isolated from the Chinese herb Huang Qui, namely baicalin, baicalein, and wogonin, were examined for their effects on LPS-induced nitric oxide (NO) production and iNOS and COX-2 gene expressions in RAW 264.7 macrophages. The results indicated that these three polyphenolic compounds inhibited LPS-induced NO production in a concentration-dependent manner without a notable cytotoxic effect on these cells. The decrease in NO production was in parallel with the inhibition by these polyphenolic compounds of LPS-induced iNOS gene expression. However, these three compounds did not directly affect iNOS enzyme activity. In addition, wogonin, but not baicalin or baicalein, inhibited LPS-induced prostaglandin E2 (PGE2) production and COX-2 gene expression without affecting COX-2 enzyme activity. Furthermore, N-nitro-L-arginine (NLA) and N-nitro-L-arginine methyl ester (L-NAME) pretreatment enhanced LPS-induced iNOS (but not COX-2) protein expression, which was inhibited by these three polyphenolic compounds. Wogonin, but not baicalin or baicalein, similarly inhibited PGE2 production and COX-2 protein expression in NLA/LPS or L-NAME/LPS-co-treated RAW 264.7 cells. These results indicated that co-treatment with NOS inhibitors and polyphenolic compounds such as wogonin effectively blocks acute production of NO and, at the same time, inhibits expression of iNOS and COX-2 genes.
机译:我们先前曾报道过,多酚化合物Oroxylin A是脂多糖(LPS)诱导的可诱导型一氧化氮合酶(iNOS)和环氧合酶2(COX-2)表达的有效抑制剂。在本研究中,检查了从中草药黄Qui中分离出的三种与山梨素A结构相关的多酚,即黄in苷,黄e素和渥草精,它们对LPS诱导的一氧化氮(NO)产生以及iNOS和COX-2基因表达的影响在RAW 264.7巨噬细胞中。结果表明,这三种多酚化合物以浓度依赖的方式抑制LPS诱导的NO产生,而对这些细胞没有明显的细胞毒性作用。 NO产生的减少与这些多酚化合物对LPS诱导的iNOS基因表达的抑制作用平行。但是,这三种化合物并不直接影响iNOS酶的活性。此外,沃戈宁可抑制LPS诱导的前列腺素E2(PGE2)的产生和COX-2基因表达,但不影响黄X苷或黄ical素,而不会影响COX-2酶的活性。此外,N-硝基-L-精氨酸(NLA)和N-硝基-L-精氨酸甲酯(L-NAME)预处理增强了LPS诱导的iNOS(但不是COX-2)蛋白表达,这被这三种多酚抑制化合物。 Wogonin,但不是黄ical素或黄ical素,同样抑制NLA / LPS或L-NAME / LPS共同处理的RAW 264.7细胞中PGE2的产生和COX-2蛋白的表达。这些结果表明,与NOS抑制剂和多酚类化合物(如wogonin)共同处理可有效阻断NO的急性产生,同时抑制iNOS和COX-2基因的表达。

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