Cardiovascular Division, British Heart Foundation Centre of Research Excellence, School of Medicine, King's College London, 150 Stamford Street, London SE1 9NH, UK.
Mol Aspects Med. 2010 Dec;31(6):468-77. doi: 10.1016/j.mam.2010.09.003. Epub 2010 Sep 15.
During the past decade nutrigenomic studies in humans, animal models and cultured cells have provided important and novel insights into the mechanisms by which dietary isoflavones afford protection against vascular dysfunction through the amelioration of oxidative modifications and upregulation of endogenous antioxidant signaling pathways. In this review, we highlight that increased generation of nitric oxide (NO) and reactive oxygen species (ROS) in the vessel wall in response to dietary isoflavones enhance the activity of antioxidant defense enzymes in endothelial and smooth muscle cells. The estrogenic properties of isoflavones are likely to contribute to the molecular mechanisms by which these compounds activate signal transduction pathways involved in sustaining endothelial function and transcriptional activation of antioxidant defense genes in vascular cells. We evaluate the recent literature that estrogenic and hormetic properties of phytoestrogens are of benefit for the maintenance of vascular function, and conclude that dietary isoflavones can protect against cardiovascular diseases by virtue of their ability to activate signaling pathways leading to increased NO bioavailability and regulation of phase II and antioxidant enzyme expression via the redox sensitive transcription factor Nrf2. In context of epigenetics and the developmental origins of adult disease, it is noteworthy that exposure to dietary soy during fetal development reduces the susceptibility to CVD and obesity in adulthood. Thus, the Nrf2/Keap1 defense pathway provides a key mechanism by which isoflavones can act as hormetic agents to modulate intracellular redox signaling in the vasculature to prolong healthspan and reduce the incidence of age-related cardiovascular diseases.
在过去的十年中,人类、动物模型和培养细胞的营养基因组学研究为饮食异黄酮通过改善氧化修饰和上调内源性抗氧化信号通路来提供血管功能障碍保护的机制提供了重要的新见解。在这篇综述中,我们强调,饮食异黄酮在血管壁中产生的一氧化氮 (NO) 和活性氧 (ROS) 的增加,增强了内皮细胞和平滑肌细胞中抗氧化防御酶的活性。异黄酮的雌激素特性可能有助于这些化合物通过激活涉及维持内皮功能和血管细胞抗氧化防御基因转录激活的信号转导途径的分子机制。我们评估了最近的文献,即植物雌激素的雌激素和毒物兴奋效应特性有益于维持血管功能,并得出结论,饮食异黄酮可以通过激活导致 NO 生物利用度增加的信号通路来预防心血管疾病,以及通过氧化还原敏感转录因子 Nrf2 调节 II 期和抗氧化酶表达。在表观遗传学和成人疾病的发育起源方面,值得注意的是,在胎儿发育过程中暴露于饮食大豆会降低成年后患 CVD 和肥胖的易感性。因此,Nrf2/Keap1 防御途径提供了一个关键机制,异黄酮可以作为毒物兴奋剂来调节血管内细胞内氧化还原信号,延长健康寿命并降低与年龄相关的心血管疾病的发病率。