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原花青素和多不饱和脂肪酸对脂多糖激活的 RAW 264.7 巨噬细胞炎症的相加、拮抗和协同作用。

Additive, antagonistic, and synergistic effects of procyanidins and polyunsaturated fatty acids over inflammation in RAW 264.7 macrophages activated by lipopolysaccharide.

机构信息

Departament de Bioquímica i Biotecnologia, Universitat Rovira i Virgili, Tarragona, Spain.

出版信息

Nutrition. 2012 Apr;28(4):447-57. doi: 10.1016/j.nut.2011.07.027. Epub 2011 Dec 14.

DOI:10.1016/j.nut.2011.07.027
PMID:22169119
Abstract

OBJECTIVE

Macrophages play an important role in immunogenic challenges and can aggravate and propagate local inflammation. Nuclear factor-kappa B (NF-κB) and activator protein 1 pathways can regulate these inflammatory processes by modulating expression of proinflammatory genes. Bioactive molecules present in food, such as procyanidins and polyunsaturated fatty acids, possess antiinflammatory effects in vivo and in vitro. Our aim was to assess whether they have synergistic antiinflammatory effects in murine macrophages.

METHODS

A nitric oxide production assay, a phosphoprotein assay, and a low-density array for 91-gene expression related to inflammation, oxidative stress, and metabolism were performed to assess the synergistic antiinflammatory effects of dimeric procyanidins (B1, B2, B3, B4) (5 μg/mL), and the polyunsaturated fatty acids, docosahexaenoic acid, and eicosapentaenoic acid (30 μM) coincubated with lipopolysaccharide for 19 h to mimic inflammation in RAW 264.7 macrophages (mouse leukaemic monocyte macrophage cell line).

RESULTS

Adding eicosapentaenoic acid plus B3 had synergistic effects leading to decreased nitric oxide levels; the modulation of phosphoprotein levels, such as P-nuclear factor-[kappa] B p65 and P-stress-activated protein kinase/Jun-amino-terminal kinase; the down-regulation of proinflammatory genes, such as interleukins, chemokines, transcription factors; and up-regulation of antioxidant genes.

CONCLUSION

This combination has a stronger antiinflammatory effect than either of these molecules separately in RAW macrophages. These results could lead to in vivo studies that may yield novel preventive or palliative nutritional treatments for obesity, atherosclerosis, and cardiovascular diseases.

摘要

目的

巨噬细胞在免疫原性挑战中发挥重要作用,可加重和传播局部炎症。核因子-κB(NF-κB)和激活蛋白 1 途径可通过调节促炎基因的表达来调节这些炎症过程。食物中的生物活性分子,如原花青素和多不饱和脂肪酸,具有体内和体外的抗炎作用。我们的目的是评估它们在鼠巨噬细胞中是否具有协同抗炎作用。

方法

进行一氧化氮产生测定、磷酸蛋白测定和低浓度芯片 91 个与炎症、氧化应激和代谢相关的基因表达,以评估二聚原花青素(B1、B2、B3、B4)(5μg/mL)和多不饱和脂肪酸二十二碳六烯酸和二十碳五烯酸(30μM)与脂多糖共孵育 19 小时以模拟 RAW 264.7 巨噬细胞(小鼠白血病单核巨噬细胞细胞系)中的炎症的协同抗炎作用。

结果

添加二十碳五烯酸加 B3 具有协同作用,可降低一氧化氮水平;磷酸蛋白水平(如核因子-[kappa]B p65 和应激激活蛋白激酶/Jun-氨基末端激酶的 P 型)的调节;促炎基因(如白细胞介素、趋化因子、转录因子)的下调;抗氧化基因的上调。

结论

这种组合在 RAW 巨噬细胞中的抗炎作用强于这些分子中的任何一种单独作用。这些结果可能导致体内研究,为肥胖、动脉粥样硬化和心血管疾病提供新的预防或姑息性营养治疗。

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