Institute for Geriatrics and Rehabilitation, Beijing Geriatric Hospital, Beijing 100095, China.
Division of Geriatric Medicine and Gerontology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA.
Oxid Med Cell Longev. 2018 Oct 8;2018:1972714. doi: 10.1155/2018/1972714. eCollection 2018.
Oxidative damage, mitochondrial dysfunction, and neuroinflammation are strongly implicated in the pathogenesis of neurodegenerative diseases including Alzheimer's disease (AD) and Parkinson's disease (PD), and a substantial portion of elderly population at risk of these diseases requires nutritional intervention to benefit health due to lack of clinically relevant drugs. To this end, anti-inflammatory mechanisms of several phytochemicals such as curcumin, resveratrol, propolis, polyunsaturated fatty acids (PUFAs), and ginsenosides have been extensively studied. However, correlation of the phytochemicals with neuroinflammation or brain nutrition is not fully considered, especially in their therapeutic mechanism for neuronal damage or dysfunction. In this article, we review the advance in antioxidative and anti-inflammatory effects of phytochemicals and discuss the potential communication with brain microenvironment by improved gastrointestinal function, enhanced systemic immunity, and neuroprotective outcomes. These data show that phytochemicals may modulate and suppress neuroinflammation of the brain by several approaches: (1) reducing systemic inflammation and infiltration via the blood-brain barrier (BBB), (2) direct permeation into the brain parenchyma leading to neuroprotection, (3) enhancing integrity of disrupted BBB, and (4) vagal reflex-mediated nutrition and protection by gastrointestinal function signaling to the brain. Therefore, many phytochemicals have multiple potential neuroprotective approaches contributing to therapeutic benefit for pathogenesis of neurodegenerative diseases, and development of strategies for preventing these diseases represents a considerable public health concern and socioeconomic burden.
氧化损伤、线粒体功能障碍和神经炎症强烈参与了神经退行性疾病的发病机制,包括阿尔茨海默病 (AD) 和帕金森病 (PD),由于缺乏临床相关药物,相当一部分老年高危人群需要营养干预来促进健康。为此,人们广泛研究了姜黄素、白藜芦醇、蜂胶、多不饱和脂肪酸 (PUFA) 和人参皂苷等几种植物化学物质的抗炎机制。然而,植物化学物质与神经炎症或大脑营养之间的相关性并未得到充分考虑,特别是在其治疗神经元损伤或功能障碍的机制方面。在本文中,我们综述了植物化学物质的抗氧化和抗炎作用的最新进展,并讨论了通过改善胃肠道功能、增强全身免疫力和神经保护作用与大脑微环境的潜在交流。这些数据表明,植物化学物质可能通过几种途径来调节和抑制大脑的神经炎症:(1) 通过血脑屏障 (BBB) 减少全身炎症和浸润,(2) 直接渗透到脑组织中导致神经保护,(3) 增强受损 BBB 的完整性,以及 (4) 通过胃肠道功能向大脑发出信号来实现迷走神经反射介导的营养和保护。因此,许多植物化学物质具有多种潜在的神经保护方法,有助于治疗神经退行性疾病的发病机制,而制定预防这些疾病的策略是一个相当大的公共卫生关注和社会经济负担。