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燕麦中的多酚 avenanthramides 具有抗炎和止痒活性。

Avenanthramides, polyphenols from oats, exhibit anti-inflammatory and anti-itch activity.

作者信息

Sur Runa, Nigam Anu, Grote Devon, Liebel Frank, Southall Michael D

机构信息

Preclinical Pharmacology, Skin Research Center, Johnson & Johnson Consumer Products, 199 Grandview Road, Skillman, NJ 08558, USA.

出版信息

Arch Dermatol Res. 2008 Nov;300(10):569-74. doi: 10.1007/s00403-008-0858-x. Epub 2008 May 7.

Abstract

Oatmeal has been used for centuries as a soothing agent to relieve itch and irritation associated with various xerotic dermatoses; however few studies have sought to identify the active phytochemical(s) in oat that mediate this anti-inflammatory activity. Avenanthramides are phenolic compounds present in oats at approximately 300 parts per million (ppm) and have been reported to exhibit anti-oxidant activity in various cell-types. In the current study we investigated whether these compounds exert anti-inflammatory activity in the skin. We found that avenanthramides at concentrations as low as 1 parts per billion inhibited the degradation of inhibitor of nuclear factor kappa B-alpha (IkappaB-alpha) in keratinocytes which correlated with decreased phosphorylation of p65 subunit of nuclear factor kappa B (NF-kappaB). Furthermore, cells treated with avenanthramides showed a significant inhibition of tumor necrosis factor-alpha (TNF-alpha) induced NF-kappaB luciferase activity and subsequent reduction of interleukin-8 (IL-8) release. Additionally, topical application of 1-3 ppm avenanthramides mitigated inflammation in murine models of contact hypersensitivity and neurogenic inflammation and reduced pruritogen-induced scratching in a murine itch model. Taken together these results demonstrate that avenanthramides are potent anti-inflammatory agents that appear to mediate the anti-irritant effects of oats.

摘要

几个世纪以来,燕麦片一直被用作一种舒缓剂,以缓解与各种干性皮肤病相关的瘙痒和刺激;然而,很少有研究试图确定燕麦中介导这种抗炎活性的活性植物化学物质。燕麦酰胺是燕麦中存在的酚类化合物,含量约为百万分之300(ppm),据报道在各种细胞类型中具有抗氧化活性。在本研究中,我们调查了这些化合物是否在皮肤中发挥抗炎活性。我们发现,浓度低至十亿分之一的燕麦酰胺可抑制角质形成细胞中核因子κBα抑制剂(IkappaBα)的降解,这与核因子κB(NF-κB)p65亚基磷酸化减少相关。此外,用燕麦酰胺处理的细胞显示出对肿瘤坏死因子-α(TNF-α)诱导的NF-κB荧光素酶活性有显著抑制作用,并随后减少白细胞介素-8(IL-8)的释放。此外,局部应用1-3 ppm的燕麦酰胺可减轻接触性超敏反应和神经源性炎症小鼠模型中的炎症,并减少小鼠瘙痒模型中致痒原诱导的抓挠。综上所述,这些结果表明燕麦酰胺是有效的抗炎剂,似乎介导了燕麦的抗刺激作用。

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