Toxicology and Disease Group, Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Toxicology and Disease Group, Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran; Department of Toxicology and Pharmacology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran; International Campus, Tehran University of Medical Sciences, (IC-TUMS), Tehran, Iran.
Ageing Res Rev. 2017 Jul;36:11-19. doi: 10.1016/j.arr.2017.02.004. Epub 2017 Feb 21.
A wide array of cell signaling mediators and their interactions play vital roles in neuroinflammation associated with ischemia, brain trauma, developmental disorders and age-related neurodegeneration. Along with neurons, microglia and astrocytes are also affected by the inflammatory cascade by releasing pro-inflammatory cytokines, chemokines and reactive oxygen species. The release of pro-inflammatory mediators in response to neural dysfunction may be helpful, neutral or even deleterious to normal cellular survival. Moreover, the important role of NF-κB factors in the central nervous system (CNS) through toll-like receptor (TLR) activation has been well established. This review demonstrates recent findings regarding therapeutic aspects of polyphenolic compounds for the treatment of neuroinflammation, with the aim of regulating TLR4. Polyphenols including flavonoids, phenolic acids, phenolic alcohols, stilbenes and lignans, can target TLR4 signaling pathways in multiple ways. Toll interacting protein expression could be modulated by epigallocatechin-3-gallate. Resveratrol may also exert neuroprotective effects via the TLR4/NF-κB/STAT signaling cascade. Its role in activation of cascade via interfering with TLR4 oligomerization upon receptor stimulation has also been reported. Curcumin, another polyphenol, can suppress overexpression of inflammatory mediators via inhibiting the TLR4-MAPK/NF-κB pathway. It can also reduce neuronal apoptosis via a mechanism concerning the TLR4/MyD88/NF-κB signaling pathway in microglia/macrophages. Despite a symphony of in vivo and in vitro studies, many molecular and pharmacological aspects of neuroinflammation remain unclear. It is proposed that natural compounds targeting TLR4 may serve as important pharmacophores for the development of potent drugs for the treatment of neurological disorders.
多种细胞信号转导介质及其相互作用在与缺血、脑创伤、发育障碍和与年龄相关的神经退行性变相关的神经炎症中起着至关重要的作用。除神经元外,小胶质细胞和星形胶质细胞也受到炎症级联反应的影响,释放促炎细胞因子、趋化因子和活性氧。针对神经功能障碍释放促炎介质可能对正常细胞存活有帮助、中性甚至有害。此外,NF-κB 因子通过 Toll 样受体 (TLR) 激活在中枢神经系统 (CNS) 中的重要作用已得到充分证实。这篇综述展示了关于多酚化合物治疗神经炎症的治疗方面的最新发现,旨在调节 TLR4。多酚包括类黄酮、酚酸、酚醇、芪和木脂素,可以通过多种方式靶向 TLR4 信号通路。通过表没食子儿茶素-3-没食子酸酯可以调节 Toll 相互作用蛋白的表达。白藜芦醇也可以通过 TLR4/NF-κB/STAT 信号级联发挥神经保护作用。据报道,它还通过干扰 TLR4 寡聚化在受体刺激时发挥作用。另一种多酚姜黄素可以通过抑制 TLR4-MAPK/NF-κB 途径来抑制炎症介质的过度表达。它还可以通过 TLR4/MyD88/NF-κB 信号通路在小胶质细胞/巨噬细胞中减少神经元凋亡。尽管有大量的体内和体外研究,但神经炎症的许多分子和药理学方面仍然不清楚。有人提出,针对 TLR4 的天然化合物可能成为开发治疗神经紊乱有效药物的重要药效团。