Departamento de Nutrición y Bromatología, Toxicología y Medicina Legal, Facultad de Farmacia , Universidad de Sevilla , C/Profesor García González 2 , 41012 , Sevilla , Spain.
Instituto de Investigación y Formación Agraria y Pesquera (IFAPA), Centro Rancho de la Merced , Consejería de Agricultura, Pesca y Desarrollo Rural (CAPDA) , Junta de Andalucía, Carretera Trebujena, Km 2.1 , 11471 Jerez de la Frontera , Spain.
J Agric Food Chem. 2019 Apr 10;67(14):3909-3918. doi: 10.1021/acs.jafc.9b00282. Epub 2019 Mar 28.
Stilbenes are phenolic compounds present in different higher plant families that have shown different biological activities, such as antioxidant properties and antitumoral and anti-atherosclerotic effects, among others. Angiogenesis is a key process involved in both cancer and cardiovascular diseases, the vascular endothelial growth factor (VEGF) and its receptor VEGFR-2 being the main triggers. Certain polyphenol compounds, such as flavonoids, have shown a potent capacity to inhibit VEGF and, consequently, angiogenesis. The present work, therefore, aims to evaluate the potential effect of stilbenes on inhibiting VEGF and their subsequent effect on the downstream signaling pathway (PLCγ1, Akt, and eNOS). VEGFR-2 activation was studied through an ELISA assay in the HUVEC line, while the phosphorylation of intracellular downstream proteins PLCγ1, Akt, and eNOS was tested by Western blot. Student's t test was used to determine significant differences between samples. On the one hand, astringin, pallidol, and ω-viniferin showed the lowest IC values (2.90 ± 0.27, 4.42 ± 0.67, and 6.10 ± 1.29 μM, respectively) against VEGFR-2 activation. Additionally, VEGF-induced PLCγ1 phosphorylation was significantly inhibited by ε-viniferin, astringin, and ω-viniferin. However, ε-viniferin and pallidol simultaneously enhanced eNOS activation, proving to be via Akt activation in the case of ε-viniferin. For the first time, these data suggest that stilbenes such as astringin, pallidol, ω-viniferin, and ε-viniferin have a potential anti-angiogenic effect and they could be further considered as anti-VEGF ingredients in food and beverages. In addition, ε-viniferin and pallidol significantly allowed eNOS activation and could likely prevent the side effects caused by anti-VEGF hypertension drugs.
二苯乙烯类化合物是存在于不同高等植物科中的酚类化合物,具有不同的生物活性,如抗氧化特性以及抗肿瘤和抗动脉粥样硬化作用等。血管生成是癌症和心血管疾病都涉及的关键过程,血管内皮生长因子 (VEGF) 及其受体 VEGFR-2 是主要触发因素。某些多酚化合物,如类黄酮,已显示出抑制 VEGF 的强大能力,从而抑制血管生成。因此,本工作旨在评估二苯乙烯类化合物抑制 VEGF 的潜在作用及其对下游信号通路(PLCγ1、Akt 和 eNOS)的后续影响。通过在 HUVEC 系中进行 ELISA 测定来研究 VEGFR-2 的激活,通过 Western blot 测定细胞内下游蛋白 PLCγ1、Akt 和 eNOS 的磷酸化。使用学生 t 检验来确定样品之间的显著差异。一方面,鞣花酸、苍白醇和 ω-viniferin 对 VEGFR-2 激活的 IC 值最低(分别为 2.90 ± 0.27、4.42 ± 0.67 和 6.10 ± 1.29 μM)。此外,ε-viniferin、鞣花酸和 ω-viniferin 显著抑制了 VEGF 诱导的 PLCγ1 磷酸化。然而,ε-viniferin 和苍白醇同时增强了 eNOS 的激活,对于 ε-viniferin 来说,这是通过 Akt 激活实现的。这些数据首次表明,鞣花酸、苍白醇、ω-viniferin 和 ε-viniferin 等二苯乙烯类化合物具有潜在的抗血管生成作用,它们可以进一步被考虑作为食品和饮料中的抗 VEGF 成分。此外,ε-viniferin 和苍白醇显著允许 eNOS 激活,并且可能预防抗 VEGF 高血压药物引起的副作用。