黄酮醇非瑟酮防治神经系统疾病。

Pamela Maher
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引用次数: 29

摘要

神经系统疾病,包括神经退行性疾病,对患者和整个社会都有重大的负面影响。由于大多数这些疾病的患病率随着年龄的增长而增加,我们老龄化人口的后果只会越来越严重。现在人们认识到,神经系统疾病是多因素的,涉及多个细胞系统的破坏。虽然每种疾病都有特定的启动机制和病理,但某些共同的途径似乎与大多数(如果不是全部的话)神经系统疾病有关。因此,识别能够调节多种途径促进疾病发展或进展的化合物变得越来越重要。其中一种化合物是黄酮醇非瑟酮。非塞汀现已在临床前模型中显示,可有效预防多种神经系统疾病的发生和/或进展,包括阿尔茨海默病、帕金森病、亨廷顿病、肌萎缩侧索硬化症、中风(缺血性和出血性)和创伤性脑损伤,以及减少大脑中与年龄相关的变化。这些有益作用源于它对与不同神经系统疾病相关的多种途径的作用。这些作用包括其众所周知的抗炎和抗氧化作用,以及最近被描述的对受调节的细胞死亡氧中毒/铁中毒途径、肠道微生物群及其抗衰老活性的影响。因此,越来越多的临床前数据,以及非瑟酮调节大量与脑功能障碍相关的通路的能力,强烈表明,在人类中追求其治疗效果是值得的。
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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Preventing and Treating Neurological Disorders with the Flavonol Fisetin.

Neurological disorders, including neurodegenerative diseases, have a significant negative impact on both patients and society at large. Since the prevalence of most of these disorders increases with age, the consequences for our aging population are only going to grow. It is now acknowledged that neurological disorders are multi-factorial involving disruptions in multiple cellular systems. While each disorder has specific initiating mechanisms and pathologies, certain common pathways appear to be involved in most, if not all, neurological disorders. Thus, it is becoming increasingly important to identify compounds that can modulate the multiple pathways that contribute to disease development or progression. One of these compounds is the flavonol fisetin. Fisetin has now been shown in preclinical models to be effective at preventing the development and/or progression of multiple neurological disorders including Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, stroke (both ischemic and hemorrhagic) and traumatic brain injury as well as to reduce age-associated changes in the brain. These beneficial effects stem from its actions on multiple pathways associated with the different neurological disorders. These actions include its well characterized anti-inflammatory and anti-oxidant effects as well as more recently described effects on the regulated cell death oxytosis/ferroptosis pathway, the gut microbiome and its senolytic activity. Therefore, the growing body of pre-clinical data, along with fisetin's ability to modulate a large number of pathways associated with brain dysfunction, strongly suggest that it would be worthwhile to pursue its therapeutic effects in humans.

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Erratum to: Flavonoids as an Intervention for Alzheimer's Disease: Progress and Hurdles Towards Defining a Mechanism of Action. Maintaining a Dynamic Brain: A Review of Empirical Findings Describing the Roles of Exercise, Learning, and Environmental Enrichment in Neuroplasticity from 2017-2023. The Multifaceted Effects of Flavonoids on Neuroplasticity Nicotinamide Mononucleotide Prevents Cisplatin-Induced Mitochondrial Defects in Cortical Neurons Derived from Human Induced Pluripotent Stem Cells. Proceedings from the Albert Charitable Trust Inaugural Workshop on 'Understanding the Acute Effects of Exercise on the Brain'.
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