黄酮类化合物作为阿尔茨海默病的干预措施:确定作用机制的进展与障碍。

Katriona L Hole, Robert J Williams
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引用次数: 0

摘要

迄今为止,通过靶向淀粉样蛋白 β(Aβ)来开发改变阿尔茨海默病(AD)病情的干预措施的尝试尚未成功。因此,我们需要针对其他靶点的新型疗法,以及适合早期和持续使用的方法,这可能是预防阿尔茨海默病所必需的。大量体外和体内研究表明,类黄酮可在与AD相关的过程和途径中发挥作用,如Aβ和tau病理学、BDNF的增加、炎症、氧化应激和神经发生。然而,由于一直缺乏明确的机理数据,无法充分考虑黄酮类化合物在体内的代谢和生物利用度,因此阻碍了黄酮类化合物的治疗开发。本综述将重点关注将这些因素纳入实验设计的研究,并将评估开发特定类黄酮作为AD疗法的证据。鉴于目前抗Aβ靶向治疗缺乏成功案例,本综述将特别关注类黄酮介导的tau磷酸化和聚集调节,因为这方面的研究同样缺乏。在对这些证据进行反思的基础上,我们还将研究阻碍类黄酮疗法发展的障碍。最后,还将探讨类黄酮代谢组学的最新进展、微生物组对类黄酮治疗AD能力的改变和影响。本综述通过强调类黄酮针对AD病理学多个方面的潜力以及考虑存在的障碍,旨在促进高效和有效地确定基于类黄酮的方法,这些方法具有作为AD治疗干预措施的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Flavonoids as an Intervention for Alzheimer's Disease: Progress and Hurdles Towards Defining a Mechanism of Action.

Attempts to develop a disease modifying intervention for Alzheimer's disease (AD) through targeting amyloid β (Aβ) have so far been unsuccessful. There is, therefore, a need for novel therapeutics against alternative targets coupled with approaches which may be suitable for early and sustained use likely required for AD prevention. Numerous in vitro and in vivo studies have shown that flavonoids can act within processes and pathways relevant to AD, such as Aβ and tau pathology, increases in BDNF, inflammation, oxidative stress and neurogenesis. However, the therapeutic development of flavonoids has been hindered by an ongoing lack of clear mechanistic data that fully takes into consideration metabolism and bioavailability of flavonoids in vivo. With a focus on studies that incorporate these considerations into their experimental design, this review will evaluate the evidence for developing specific flavonoids as therapeutics for AD. Given the current lack of success of anti-Aβ targeting therapeutics, particular attention will be given to flavonoid-mediated regulation of tau phosphorylation and aggregation, where there is a comparable lack of study. Reflecting on this evidence, the obstacles that prevent therapeutic development of flavonoids will be examined. Finally, the significance of recent advances in flavonoid metabolomics, modifications and influence of the microbiome on the therapeutic capacity of flavonoids in AD are explored. By highlighting the potential of flavonoids to target multiple aspects of AD pathology, as well as considering the hurdles, this review aims to promote the efficient and effective identification of flavonoid-based approaches that have potential as therapeutic interventions for AD.

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