کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1185090 1492080 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Effect of pecan phenolics on the release of nitric oxide from murine RAW 264.7 macrophage cells
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Effect of pecan phenolics on the release of nitric oxide from murine RAW 264.7 macrophage cells
چکیده انگلیسی


• Pecan phenolics impart anti-inflammatory activity to LPS-stimulated RAW 264.7 macrophages.
• Phenolic acids & small PACs have a dose-dependent effect at curbing inflammation in the cell model.
• The low-molecular-weight compounds comprise catechin, gallic acid and ellagic acid derivatives.
• Cytotoxicity and phenolic–LPS complexation are not responsible for the anti-inflammation.
• This is the first reporting of pecan phenolics possessing anti-inflammatory activity.

Inflammation is linked to numerous chronic disease states. Phenolic compounds have attracted attention because a number of these compounds possess anti-inflammatory properties. A phenolic crude extract was prepared from pecans and separated by Sephadex LH-20 column chromatography into low- and high-molecular-weight (LMW/HMW) fractions. Anti-inflammatory properties of these fractions were assessed in LPS-stimulated RAW 264.7 murine macrophage cells. NO and reactive oxygen species (ROS) production was monitored after 3 different experimental protocols: (1) pre-treatment with Escherichia coli O111:B4 lipopolysaccharide (LPS); (2) pre-treatment with a pecan crude extract and its fractions; and (3) co-incubation of LPS with a pecan crude extract and its fractions. The LMW fraction displayed a dose-dependent decrease in NO production and a significant decrease from the LPS control in ROS production when cells were either co-incubated with or pre-treated with LPS. The phenolics were characterized by HPLC to help identify those responsible for the observed effect.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Food Chemistry - Volume 212, 1 December 2016, Pages 681–687
نویسندگان
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