McCarty Mark F
Natural Alternatives International, 1185 Linda Vista Dr., San Marcos, CA 92078, United States.
Med Hypotheses. 2008;70(1):170-81. doi: 10.1016/j.mehy.2005.09.058. Epub 2007 Sep 6.
Ample intakes of fruit and vegetables have been linked epidemiologically with reduced risk for coronary disease, stroke, hypertension, obesity, many types of cancer, chronic pulmonary disease, osteoporosis, and various ocular disorders. The favorable impact of diets rich in fruit and vegetables on coronary risk has been confirmed in meta-analyses, and is thought to be largely attributable to the folk acid and potassium supplied by these foods. Although high intakes of vitamin C appear to confer some cardiovascular protection, the amounts supplied by typical diets may be too low to be of much benefit in this regard. High flavonoid intakes emerge as protective in some epidemiological studies, albeit the dose-response pattern observed is often L-shaped - seemingly more consistent with low intakes being harmful, than with high intakes being protective. Nonetheless, flavonoids have shown anti-atherogenic activity in rodent models, and both clinical and rodent supplementation studies with foods and food extracts rich in flavonoids demonstrate improvements in endothelium-dependent vasodilation traceable to increased endothelial nitric oxide synthesis. However, flavonoids do not appear to increase the expression of endothelial NO synthase, nor do they modify endothelial superoxide production. A likely explanation is that, even in nanomolar concentrations achievable in vivo, flavonoids can act as efficient scavengers of peroxynitrite-derived radicals, thereby protecting the cofactor tetrahydrobiopterin, crucial for NO synthase activity. Studies with cultured endothelial cells should be useful for evaluating this possibility. It would also be appropriate to assess the effects of flavonoids on prostacylin synthetase activity, on endothelial catabolism of asymmetric dimethylarginine, and on signaling mechanisms that activate NO synthase. Since peroxynitrite can induce mutagenic damage to DNA, it is conceivable that scavenging of peroxynitrite-derived radicals contributes to the reduction in mutagenesis associated with high intakes of fruits and vegetables. Carotenoids also have the potential to prevent peroxynitrite-mediated damage, although, as contrasted with flavonoids, there is comparatively little evidence that these compounds are anti-atherogenic or beneficial for endothelial function; a recent meta-analysis of epidemiological studies suggests that high lutein intakes may modestly reduce coronary risk.
从流行病学角度来看,大量摄入水果和蔬菜与降低患冠心病、中风、高血压、肥胖症、多种癌症、慢性肺病、骨质疏松症及各种眼部疾病的风险相关。富含水果和蔬菜的饮食对冠心病风险的有利影响已在荟萃分析中得到证实,并且人们认为这在很大程度上归因于这些食物所提供的叶酸和钾。虽然高剂量摄入维生素C似乎能提供一定的心血管保护作用,但典型饮食所提供的维生素C量可能过低,在这方面益处不大。在一些流行病学研究中,高黄酮摄入量显示出保护作用,尽管观察到的剂量反应模式通常呈L形——似乎更符合低摄入量有害而非高摄入量有保护作用的情况。尽管如此,黄酮类化合物在啮齿动物模型中已显示出抗动脉粥样硬化活性,并且用富含黄酮类化合物的食物和食物提取物进行的临床及啮齿动物补充研究均表明,内皮依赖性血管舒张功能有所改善,这可归因于内皮一氧化氮合成增加。然而,黄酮类化合物似乎不会增加内皮型一氧化氮合酶的表达,也不会改变内皮超氧化物的产生。一个可能的解释是,即使在体内可达到的纳摩尔浓度下,黄酮类化合物也能作为过氧亚硝酸盐衍生自由基的有效清除剂,从而保护对一氧化氮合酶活性至关重要的辅因子四氢生物蝶呤。对培养的内皮细胞进行的研究应有助于评估这种可能性。评估黄酮类化合物对前列环素合成酶活性、对不对称二甲基精氨酸的内皮分解代谢以及对激活一氧化氮合酶的信号传导机制的影响也将是合适的。由于过氧亚硝酸盐可诱导对DNA的诱变损伤,可以想象,清除过氧亚硝酸盐衍生自由基有助于减少与高水果和蔬菜摄入量相关的诱变作用。类胡萝卜素也有预防过氧亚硝酸盐介导损伤的潜力,不过,与黄酮类化合物相比,相对较少有证据表明这些化合物具有抗动脉粥样硬化作用或对内皮功能有益;最近一项流行病学研究的荟萃分析表明,高叶黄素摄入量可能会适度降低冠心病风险。