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从高丽乌头根部分离得到的咖啡酰衍生物的抗氧化和抗炎作用。

The anti-oxidative and anti-inflammatory effects of caffeoyl derivatives from the roots of Aconitum koreanum R. RAYMOND.

机构信息

College of Pharmacy, Chung Ang University, Seoul 156-756, South Korea.

出版信息

Biol Pharm Bull. 2009 Dec;32(12):2029-33. doi: 10.1248/bpb.32.2029.

Abstract

Activity guided fractionation of Aconitum koreanum root extract (RAK), a traditional medicine in Korea, afforded four caffeoyl derivatives, caffeic acid (1), 4,5-dicaffeoylquinic acid (2), 3,5-dicaffeoylquinic acid (3) and 3,5-dicaffeoylquinic acid methyl ester (4). In order to evaluate the anti-oxidative and anti-inflammatory effects of these compounds, their 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activities and abilities to inhibit nitric oxide (NO) production in lipopolysaccharide (LPS)-stimulated RAW 264.7 were examined. And the protein and mRNA levels of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) in LPS-stimulated HaCaT cells were also quantified by Western blotting and reverse transcription-polymerase chain reaction (RT-PCR). Compounds (1-4) showed potent DPPH radical scavenging and NO inhibitory activities as compared with positive controls (L-ascorbic acid and N(G)-monomethyl-L-arginine (L-NMMA), respectively). Also, these compounds dose-dependently inhibited the expressions of iNOS and COX-2 as well as their mRNA levels.

摘要

从韩国传统药物乌头根提取物(RAK)中进行活性导向分离,得到了四个咖啡酰衍生物:咖啡酸(1)、4,5-二咖啡酰奎宁酸(2)、3,5-二咖啡酰奎宁酸(3)和 3,5-二咖啡酰奎宁酸甲酯(4)。为了评估这些化合物的抗氧化和抗炎作用,检测了它们对 1,1-二苯基-2-苦基肼(DPPH)自由基的清除能力以及抑制脂多糖(LPS)刺激的 RAW 264.7 细胞中一氧化氮(NO)产生的能力。通过 Western blot 和逆转录-聚合酶链反应(RT-PCR)还定量测定了 LPS 刺激的 HaCaT 细胞中诱导型一氧化氮合酶(iNOS)和环加氧酶-2(COX-2)的蛋白和 mRNA 水平。与阳性对照(L-抗坏血酸和 N(G)-单甲基-L-精氨酸(L-NMMA)相比,化合物(1-4)显示出较强的 DPPH 自由基清除和 NO 抑制活性。这些化合物还剂量依赖性地抑制了 iNOS 和 COX-2 的表达及其 mRNA 水平。

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