Dept. Biochemistry and Molecular Biology, Faculty of Sciences, University of Extremadura, Avenida de Elvas s/n, 06006 - Badajoz, Spain.
Curr Med Chem. 2011;18(8):1195-212. doi: 10.2174/092986711795029735.
The experimental evidences accumulated during last years point out a relevant role of oxidative stress in neurodegeneration. As anti-cellular oxidative stress agents flavonoids can act either as direct chemical antioxidants, the classic view of flavonoids as antioxidants, or as modulators of enzymes and metabolic and signaling pathways leading to an overshot of reactive oxygen species (ROS) formation, a more recently emerging concept. Flavonoids, a large family of natural antioxidants, undergo a significant hepatic metabolism leading to flavonoid-derived metabolites that are also bioactive as antioxidant agents. The development of more efficient flavonoid's based anti-oxidative stress therapies should also take into account their bioavailability in the brain using alternate administration protocols, and also that the major ROS triggering the cellular oxidative stress are not the same for all neurodegenerative insults and diseases. On these grounds, we have reviewed the reports on neuroprotection by different classes of flavonoids on cellular cultures and model animals. In addition, as they are now becoming valuable pharmacological drugs, due to their low toxicity, the reported adverse effects of flavonoids in model experimental animals and humans are briefly discussed.
近年来积累的实验证据表明,氧化应激在神经退行性变中起重要作用。作为抗细胞氧化应激剂,类黄酮可以作为直接的化学抗氧化剂发挥作用,这是类黄酮作为抗氧化剂的经典观点,或者作为调节酶和代谢及信号通路的调节剂,导致活性氧(ROS)形成过度,这是一个最近出现的概念。类黄酮是一大类天然抗氧化剂,经历显著的肝脏代谢,导致类黄酮衍生的代谢物也具有抗氧化剂的生物活性。为了开发更有效的基于类黄酮的抗氧化应激治疗方法,还应该考虑到它们在大脑中的生物利用度,使用替代给药方案,而且引发细胞氧化应激的主要 ROS 对于所有神经退行性损伤和疾病并不相同。基于这些原因,我们综述了不同类别的类黄酮在细胞培养和模型动物中的神经保护作用的报告。此外,由于它们的低毒性,现在已成为有价值的药理学药物,简要讨论了类黄酮在模型实验动物和人类中的报告不良反应。