Moss Joe W E, Davies Thomas S, Garaiova Iveta, Plummer Sue F, Michael Daryn R, Ramji Dipak P
School of Biosciences, Cardiff University, Cardiff, United Kingdom.
Cultech Limited, Baglan Industrial Park, Port Talbot, United Kingdom.
PLoS One. 2016 Mar 7;11(3):e0151057. doi: 10.1371/journal.pone.0151057. eCollection 2016.
Atherosclerosis is the underlying cause of cardiovascular disease that leads to more global mortalities each year than any other ailment. Consumption of active food ingredients such as phytosterols, omega-3 polyunsaturated fatty acids and flavanols are known to impart beneficial effects on cardiovascular disease although the combined actions of such agents in atherosclerosis is poorly understood. The aim of this study was to screen a nutritional supplement containing each of these active components for its anti-atherosclerotic effect on macrophages in vitro.
The supplement attenuated the expression of intercellular adhesion molecule-1 and macrophage chemoattractant protein-1 in human and murine macrophages at physiologically relevant doses. The migratory capacity of human monocytes was also hindered, possibly mediated by eicosapentaenoic acid and catechin, while the ability of foam cells to efflux cholesterol was improved. The polarisation of murine macrophages towards a pro-inflammatory phenotype was also attenuated by the supplement.
The formulation was able to hinder multiple key steps of atherosclerosis development in vitro by inhibiting monocyte recruitment, foam cell formation and macrophage polarisation towards an inflammatory phenotype. This is the first time a combination these ingredients has been shown to elicit such effects and supports its further study in preclinical in vivo models.
动脉粥样硬化是心血管疾病的根本原因,每年导致的全球死亡人数比任何其他疾病都多。已知食用植物甾醇、ω-3多不饱和脂肪酸和黄烷醇等活性食品成分对心血管疾病有有益影响,尽管这些物质在动脉粥样硬化中的联合作用尚不清楚。本研究的目的是筛选一种含有上述每种活性成分的营养补充剂,以研究其在体外对巨噬细胞的抗动脉粥样硬化作用。
该补充剂在生理相关剂量下可减弱人源和鼠源巨噬细胞中细胞间黏附分子-1和巨噬细胞趋化蛋白-1的表达。人单核细胞的迁移能力也受到阻碍,可能是由二十碳五烯酸和儿茶素介导的,同时泡沫细胞排出胆固醇的能力得到改善。该补充剂还可减弱鼠源巨噬细胞向促炎表型的极化。
该配方能够通过抑制单核细胞募集、泡沫细胞形成以及巨噬细胞向炎症表型的极化,在体外阻碍动脉粥样硬化发展的多个关键步骤。这是首次证明这些成分的组合具有此类作用,并支持在临床前体内模型中对其进行进一步研究。