Fisetin and Neurodegeneration: From Preclinical Studies to Potential Clinical Applications.

IF 3
Md Al Amin, Mehrukh Zehravi, Sherouk Hussein Sweilam, Ronald Darwin, Jeetendra Kumar Gupta, E Bhargav, G Dharmamoorthy, Voleti Vijaya Kumar, A Anka Rao, Muath Suliman, Thirunavukkarasu Periyasamy, Talha Bin Emran
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Abstract

Neurodegenerative diseases (NDs), like Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, and multiple sclerosis, pose significant challenges due to their gradual deterioration and limited available treatments. Fisetin, a naturally occurring flavonoid, has gained attention for its neuroprotective properties. This review explores the therapeutic potential of fisetin in NDs, focusing on its molecular processes and signaling pathways. Additionally, fisetin exhibits significant protective properties, particularly in reducing oxidative stress, neuroinflammation, and apoptosis. It enhances neuronal survival and reduces neuroinflammation by regulating key pathways, such as Nrf2/ARE, PI3K/Akt, and NF-κB. It also has anti-inflammatory, anti-apoptotic, and antioxidant actions. It stimulates autophagic processes, aiding in the removal of harmful protein aggregates, like tau tangles and amyloid plaques, which are hallmarks of NDs. Fisetin, as demonstrated through behavioral evaluations in animal models, has been found to improve motor coordination, synaptic plasticity, and cognitive function. Furthermore, fisetin's potential as a neuroprotective drug is emphasized by its role in enhancing autophagy and reducing tau and amyloid pathology. Research has shown its efficacy in enhancing neural resilience, synaptic plasticity, and cognitive function in both preclinical and in vitro settings. However, clinical translation remains limited due to challenges in pharmacokinetics and bioavailability, despite robust experimental evidence. Further clinical trials are needed to evaluate the safety and efficacy of fisetin, especially in early-stage NDs, explore potential synergistic effects, and understand the molecular interactions. The review demonstrates fisetin's therapeutic potential, recent research, and future strategies for NDs, highlighting bioavailability limitations and the need for new formulations or delivery systems.

非瑟酮与神经退行性变:从临床前研究到潜在的临床应用。
神经退行性疾病(NDs),如阿尔茨海默病、帕金森病、亨廷顿病、肌萎缩侧索硬化症和多发性硬化症,由于其逐渐恶化和现有治疗方法有限,构成了重大挑战。非瑟酮是一种天然存在的类黄酮,因其神经保护特性而受到关注。本文综述了非瑟酮在NDs中的治疗潜力,重点介绍了其分子过程和信号通路。此外,非瑟酮具有显著的保护作用,特别是在减少氧化应激、神经炎症和细胞凋亡方面。它通过调节Nrf2/ARE、PI3K/Akt和NF-κB等关键通路,提高神经元存活,减少神经炎症。它还具有抗炎、抗细胞凋亡和抗氧化作用。它刺激自噬过程,帮助去除有害的蛋白质聚集体,如tau缠结和淀粉样斑块,这些都是ndds的标志。通过动物模型的行为评估证明,非瑟酮可以改善运动协调、突触可塑性和认知功能。此外,非瑟酮在增强自噬和减少tau和淀粉样蛋白病理方面的作用强调了其作为神经保护药物的潜力。研究表明,在临床前和体外环境中,它在增强神经弹性、突触可塑性和认知功能方面都有功效。然而,尽管有强有力的实验证据,由于药代动力学和生物利用度方面的挑战,临床翻译仍然有限。需要进一步的临床试验来评估非瑟酮的安全性和有效性,特别是在早期NDs中,探索潜在的协同效应,并了解分子相互作用。这篇综述展示了非塞汀的治疗潜力、最近的研究和未来的NDs策略,强调了生物利用度限制和对新配方或给药系统的需求。
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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