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首页> 外文期刊>International immunopharmacology >Inhibition of inducible nitric oxide synthase and cyclooxygenase-2 expression by flavonoids isolated from Tanacetum microphyllum.
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Inhibition of inducible nitric oxide synthase and cyclooxygenase-2 expression by flavonoids isolated from Tanacetum microphyllum.

机译:从小叶艾菊中提取的类黄酮抑制一氧化氮合酶和环氧合酶-2的表达。

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摘要

Plant flavonoids show anti-inflammatory activity both in vitro and in vivo. Some flavonoids have been reported previously to inhibit nitric oxide (NO) and prostaglandin E2 (PGE2) production by suppressing inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) expression. The present study focuses on the effect of various naturally occurring flavonoids (santin, ermanin, centaureidin and 5,3'-dihydroxy-4'-methoxy-7-methoxycarbonylflavonol) on modulation of lipopolysaccharide (LPS)-induced iNOS and COX-2 expression in RAW 264.7 cells. Western blotting showed that all flavonoids suppressed the induction of both iNOS and COX-2. Ermanin and 5,3'-dihydroxy-4'-methoxy-7-methoxycarbonylflavonol were the most potent inhibitors. This study suggests that inhibition of iNOS and COX-2 expression by flavonoids may be one of the mechanisms responsible for their anti-inflammatory effects, and that they may be potential agents for use in the treatment of inflammatory diseases.
机译:植物类黄酮在体外和体内均显示出抗炎活性。以前已有一些类黄酮通过抑制诱导型一氧化氮合酶(iNOS)和环氧合酶2(COX-2)的表达来抑制一氧化氮(NO)和前列腺素E2(PGE2)的产生。本研究的重点是各种天然黄酮类化合物(桑坦,黄花青素,黄体苷和5,3'-二羟基-4'-甲氧基-7-甲氧基羰基黄酮醇)对脂多糖(LPS)诱导的iNOS和COX-2表达的调节作用。在RAW 264.7细胞中蛋白质印迹显示,所有类黄酮均抑制了iNOS和COX-2的诱导。埃尔曼宁和5,3'-二羟基-4'-甲氧基-7-甲氧基羰基黄酮醇是最有效的抑制剂。这项研究表明,类黄酮抑制iNOS和COX-2的表达可能是其抗炎作用的机制之一,并且它们可能是治疗炎性疾病的潜在药物。

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