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首页> 外文期刊>Biopharmaceutics and Drug Disposition >Effects of natural phytochemicals in Angelica sinensis (Danggui) on Nrf2-mediated gene expression of phase II drug metabolizing enzymes and anti-inflammation
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Effects of natural phytochemicals in Angelica sinensis (Danggui) on Nrf2-mediated gene expression of phase II drug metabolizing enzymes and anti-inflammation

机译:当归天然植物化学物质对Nrf2介导的Ⅱ期药物代谢酶基因表达和抗炎作用的影响

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摘要

The root of Angelica sinensis (Oliv.) Diels (abbreviated as AS) (Danggui) has a long history in Asian herbal medicine. Recently, it was demonstrated that AS possesses anti-cancer and anti-oxidant activities. Because the transcription factor Nrf2 mediates the expression of many cellular anti-oxidative stress genes, including genes that are involved in phase II drug metabolism and anti-oxidative stress, this study sought to investigate whether pure compounds from AS or an AS extract could activate antioxidant response element (ARE)-mediated gene expression and induce anti-inflammatory activities. Z-Ligustilide (Ligu), 3-butylidenephthalide (Buty) and CO2 supercritical fluid-extracted lipophilic AS extract (SFE) were tested in HepG2-C8 cells stabilized with ARE luciferase reporter gene. Ligu and Buty caused significant toxicity only at 100 μm. All three samples induced ARE-luciferase activity; however, SFE at 8.5 μg/ml induced ARE-luciferase activity 2-3 fold more potently than did either of the pure compounds. SFE also significantly increased the endogenous mRNA of Nrf2 and the Nrf2 target anti-oxidative gene NAD(P)H dehydrogenase, quinone 1 (NQO1). The protein expression of NQO1 was also significantly induced by SFE. In RAW 264.7 cells, SFE suppressed lipopolysaccharide (LPS)-induced IL-1β and TNF-α expression about 2 fold stronger than sulforaphane, whereas both pure compounds and SFE suppressed inflammatory nitric oxide (NO) production. In summary, this study demonstrates that AS has anti-inflammatory effects and activates the Nrf2 pathway, which protects against oxidative stress.
机译:当归(Oliv。)Diels(缩写为AS)(当归)的根在亚洲草药中历史悠久。最近,已证明AS具有抗癌和抗氧化活性。由于转录因子Nrf2介导许多细胞抗氧化应激基因的表达,包括参与II期药物代谢和抗氧化应激的基因,因此本研究试图研究AS或AS提取物中的纯化合物是否可以激活抗氧化剂响应元件(ARE)介导的基因表达并诱导抗炎活性。在用ARE萤光素酶报告基因稳定的HepG2-C8细胞中测试了Z--古丁内酯(Ligu),3-丁二烯(Buty)和CO2超临界流体萃取的亲脂性AS提取物(SFE)。 Ligu和Buty仅在100μm处产生明显的毒性。所有三个样品均诱导ARE-萤光素酶活性。然而,SFE的浓度为8.5μg/ ml,其诱导的ARE荧光素酶活性比任何一种纯化合物强2-3倍。 SFE还显着增加了Nrf2和Nrf2靶标抗氧化基因NAD(P)H脱氢酶醌1(NQO1)的内源性mRNA。 SFE还显着诱导NQO1的蛋白表达。在RAW 264.7细胞中,SFE抑制脂多糖(LPS)诱导的IL-1β和TNF-α表达比萝卜硫烷强约2倍,而纯化合物和SFE均抑制炎性一氧化氮(NO)的产生。总而言之,这项研究表明AS具有抗炎作用并激活Nrf2途径,从而可防止氧化应激。

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