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Synthesis of phenolic amides and evaluation of their antioxidant and anti-inflammatory activity in vitro and in vivo

机译:酚类酰胺的合成及其在体外和体内抗氧化剂和抗炎活性的评价

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摘要

A series of 15 phenolic amides (PAs) have been synthesized (PA1-PA15) and examined in vitro by four different tests: (1) prevention of Cu2+-induced human low-density lipoprotein oxidation, (2) scavenging of stable radicals, (3) anti-inflammatory activity, (4) scavenging of superoxide radicals. We used PA1 and alpha-tocopherol for an in vivo study. The overall potential of the antioxidant system was significantly enhanced by the PA1 and alpha-tocopherol supplements as the hepatic TBARS levels were lowered while the hepatic SOD activities and GSH concentration were elevated in PA1 fed rats. Our results support that PA1 may exert antioxidant action through inhibiting superoxide generation. PA1 decreased the level of nitric oxide (NO) production, tumor necrosis factor-alpha (TNF-alpha) and nuclear factor-kappa B (NF-kappa B). These results show that PA1 can inhibit lipid peroxidation, enhance the activities of antioxidant enzymes, and decrease the TNF-alpha/NF-kappa B level and nitric oxide production. Therefore, it was speculated that PA1 acts through its anti-inflammation capacity.
机译:一系列15种酚醛酰胺(PAS)已合成(PA1-PA15),并通过四种不同的试验体外检测:(1)预防Cu2 +诱导的人低密度脂蛋白氧化,(2)稳定基团的清除(2)稳定的自由基,( 3)抗炎活性,(4)超氧化物的清除。我们使用了PA1和Alpha-Tocophherol进行体内研究。 PA1和α-生育酚补充剂在PA1喂养大鼠升高时,PA1和α-生育酚补充剂显着增强了抗氧化系统的总体潜力,因为肝脏SOD活性和GSH浓度升高。我们的研究结果支持PA1可以通过抑制超氧化物产生来施加抗氧化作用。 PA1降低了一氧化氮(NO)生产,肿瘤坏死因子-α(TNF-α)和核因子-Kappa B(NF-Kappa B)的水平。这些结果表明,PA1可以抑制脂质过氧化,增强抗氧化酶的活性,降低TNF-α/ NF-κB水平和一氧化氮产生。因此,推测PA1通过其抗炎能力作用。

著录项

  • 来源
    《RSC Advances》 |2015年第104期|共10页
  • 作者单位

    Natl Taichung Univ Sci &

    Technol Dept Beauty Sci Taichung Taiwan;

    Asia Univ Dept Hlth &

    Nutr Biotechnol Taichung Taiwan;

    Chung Shan Med Univ Sch Hlth Diet &

    Ind Management Taichung Taiwan;

    Asia Univ Dept Hlth &

    Nutr Biotechnol Taichung Taiwan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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