Department of Pharmacy, Southeast University, Dhaka, Bangladesh; Pharmakon Neuroscience Research Network, Dhaka, Bangladesh.
Department of Pharmacy, BRAC University, Dhaka, Bangladesh.
Sci Total Environ. 2020 Jan 15;700:134836. doi: 10.1016/j.scitotenv.2019.134836. Epub 2019 Oct 21.
Alzheimer's disease (AD) is a progressive, chronic and severe neurodegenerative disorder linked with cognitive and memory impairment that eventually lead to death. There are several processes which can cause AD, including mitochondrial dysfunction-mediated oxidative stress (OS), intracellular buildup of hyper-phosphorylated tau as neurofibrillary tangles (NFTs) and excessive buildup of extracellular amyloid beta (Aβ) plaques, and/or genetic as well as the environmental factors. Existing treatments can only provide symptomatic relief via providing temporary palliative therapy which can weaken the rate of AD-associated cognitive decline. Plants are the fundamental building blocks for the environment and produce various secondary metabolites. Biflavonoids are one among such secondary metabolite that possesses the potential to mediate noticeable change in the aggregation of tau, Aβ and also efficiently can decrease the toxic effects of Aβ oligomers in comparison with the monoflavonoid moieties. Nevertheless, the molecular processes remain to be exposed, flavonoids are found to cause a change in the Aβ and tau aggregation pathway to generate non-toxic aggregates. In this review, we discuss the neuroprotective action of small molecule biflavonoid to reduce the neurodegenerative events of AD. Furthermore, this appraisal advances our knowledge to develop potential new targets for the treatment of AD.
阿尔茨海默病(AD)是一种进行性、慢性和严重的神经退行性疾病,与认知和记忆障碍有关,最终导致死亡。有几种过程可能导致 AD,包括线粒体功能障碍介导的氧化应激(OS)、细胞内过度磷酸化的 tau 积聚形成神经原纤维缠结(NFTs)和细胞外淀粉样β(Aβ)斑块的过度积聚,以及/或遗传和环境因素。现有的治疗方法只能通过提供暂时的姑息疗法来提供症状缓解,这种疗法可以减缓 AD 相关的认知能力下降的速度。植物是环境的基本组成部分,产生各种次生代谢物。双黄酮类化合物是其中一种次生代谢物,具有介导 tau、Aβ聚集发生显著变化的潜力,并且与单黄酮部分相比,能够有效地降低 Aβ寡聚物的毒性作用。然而,分子过程仍然有待揭示,研究发现黄酮类化合物可以改变 Aβ和 tau 的聚集途径,生成无毒的聚集物。在这篇综述中,我们讨论了小分子双黄酮的神经保护作用,以减少 AD 的神经退行性事件。此外,这项评估增进了我们对开发 AD 治疗新靶点的认识。