Efficacy and molecular mechanisms of hesperidin in mitigating Alzheimer's disease: A systematic review

IF 6 2区 医学 Q1 CHEMISTRY, MEDICINAL
Xu Han , Yuting Zhang , Lijuan Zhang , Yanyan Zhuang , Yu Wang
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引用次数: 0

Abstract

Hesperidin, a flavonoid glycoside, is a natural phenolic compound that has broad biological effects. Increasing evidence suggests that hesperidin inhibits the occurrence and development of neurodegenerative diseases, including Alzheimer's disease (AD). This article reviews the neuropharmacological mechanisms of hesperidin in the prevention and treatment of AD through in vitro and in vivo studies. A systematic review of preclinical studies was conducted using PubMed, Web of Science, Scopus, and Google Scholar (up to July 1, 2024). The neuroprotective potential of hesperidin was mediated through mechanisms such as inhibition of β-amyloid (Aβ) aggregation, enhancement of endogenous antioxidant defense functions, reduction of neuroinflammation and apoptosis, improvement of mitochondrial dysfunction, regulation of autophagy, and promotion of neurogenesis. Despite various preclinical studies on the role of hesperidin in AD, its exact effects on humans remain unclear. Few clinical trials have indicated that dietary supplements rich in hesperidin can improve cerebral blood flow, cognition, and memory performance. The neuroprotective effect of hesperidin may be exerted via regulating different molecular pathways, including the RAGE/NF-κB, Akt/Nrf2, and AMPK/BDNF/CREB pathways. However, further clinical trials are needed to confirm the neuroprotective effects of this natural flavonoid compound and to assess its safety.

Abstract Image

Abstract Image

橙皮苷减轻阿尔茨海默病的疗效和分子机制:系统综述
橙皮苷是一种具有广泛生物学效应的天然酚类化合物。越来越多的证据表明橙皮苷抑制神经退行性疾病的发生和发展,包括阿尔茨海默病(AD)。本文通过体外和体内研究综述橙皮苷预防和治疗AD的神经药理学机制。通过PubMed、Web of Science、Scopus和谷歌Scholar(截止到2024年7月1日)对临床前研究进行了系统回顾。橙皮苷的神经保护作用可能通过抑制β-淀粉样蛋白(Aβ)聚集、增强内源性抗氧化防御功能、减少神经炎症和凋亡、改善线粒体功能障碍、调节自噬和促进神经发生等机制介导。尽管对橙皮苷在阿尔茨海默病中的作用进行了各种临床前研究,但其对人类的确切影响仍不清楚。很少有临床试验表明富含橙皮苷的膳食补充剂可以改善脑血流量,认知和记忆性能。橙皮苷的神经保护作用可能通过调节RAGE/NF-κB、Akt/Nrf2、AMPK/BDNF/CREB等不同的分子通路来发挥。然而,需要进一步的临床试验来证实这种天然类黄酮化合物的神经保护作用并评估其安全性。
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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