Department of Cardiology, Rambam Health Care Campus, Haifa, Israel.
Am J Clin Nutr. 2010 Jul;92(1):161-9. doi: 10.3945/ajcn.2009.28408. Epub 2010 Apr 14.
Endothelial progenitor cells (EPCs) contribute to the maintenance of vascular endothelial function. The moderate consumption of red wine provides cardiovascular protection.
We investigated the underlying molecular mechanism of EPC migration in young, healthy individuals who drank red wine.
Fourteen healthy volunteers consumed 250 mL red wine daily for 21 consecutive days. Vascular endothelial function, plasma stromal cell-derived factor 1alpha (SDF1alpha) concentrations, and the number, migration, and nitric oxide production of EPCs were determined before and after the daily consumption of red wine. EPCs were glucose stressed to study the effect of red wine on EPC migration, proliferation, and senescence and to study the expressions of CXC chemokine receptor 4 (CXCR4) and members of the Pi3K/Akt/eNOS (phosphatidylinositol 3-kinase/protein kinase B/endothelial nitric oxide synthase) signaling pathway by Western blotting.
Daily red wine consumption for 21 consecutive days significantly enhanced vascular endothelial function. Although plasma SDF1alpha concentrations were unchanged, EPC count and migration were significantly increased after this 21-d consumption period. Red wine increased the migration, proliferation, CXCR4 expression, and activity of the Pi3K/Akt/eNOS signaling pathway and decreased the extent of apoptosis in glucose-stressed EPCs.
The results of the present study indicate that red wine exerts its effect through the up-regulation of CXCR4 expression and activation of the SDF1alpha/CXCR4/Pi3K/Akt/eNOS signaling pathway, which results in increased EPC migration and proliferation and decreased extent of apoptosis. Our findings suggest that these effects could be linked to the mechanism of cardiovascular protection that is associated with the regular consumption of red wine.
内皮祖细胞(EPCs)有助于维持血管内皮功能。适量饮用红酒可提供心血管保护。
我们研究了年轻健康个体饮用红酒后 EPC 迁移的潜在分子机制。
14 名健康志愿者连续 21 天每天饮用 250 毫升红酒。在每天饮用红酒前后,测定血管内皮功能、血浆基质细胞衍生因子 1α(SDF1α)浓度以及 EPC 的数量、迁移和一氧化氮产生。对 EPC 进行葡萄糖应激处理,以研究红酒对 EPC 迁移、增殖和衰老的影响,并研究 CXC 趋化因子受体 4(CXCR4)和 Pi3K/Akt/eNOS(磷脂酰肌醇 3-激酶/蛋白激酶 B/内皮型一氧化氮合酶)信号通路成员的表达情况,Western 印迹法。
连续 21 天每天饮用红酒可显著增强血管内皮功能。尽管血浆 SDF1α浓度不变,但经过 21 天的饮用期后,EPC 数量和迁移明显增加。红酒增加了葡萄糖应激 EPC 的迁移、增殖、CXCR4 表达和 Pi3K/Akt/eNOS 信号通路的活性,并降低了 EPC 的凋亡程度。
本研究结果表明,红酒通过上调 CXCR4 表达和激活 SDF1α/CXCR4/Pi3K/Akt/eNOS 信号通路发挥作用,从而增加 EPC 的迁移和增殖,减少凋亡程度。我们的发现表明,这些影响可能与与红酒规律饮用相关的心血管保护机制有关。