单胺氧化酶与神经退行性变:治疗干预的机制、抑制剂和天然化合物。

IF 4.4 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Chayan Banerjee , Debasmita Tripathy , Deepak Kumar , Joy Chakraborty
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引用次数: 0

摘要

哺乳动物黄酶类单胺氧化酶(MAO)位于线粒体外膜(OMM)上,参与大脑中不同单胺神经递质的代谢。在 MAO 介导的相关底物氧化脱氨过程中,会释放出 H2O2 作为催化副产物,从而成为活性氧(ROS)的主要来源。据报道,在正常情况下,MAO 介导的 ROS 可促进线粒体电子传递链的运作和多巴胺的阶段性释放。然而,由于其定位在线粒体上,其酶活性的突然升高会直接影响细胞器的形态和功能。例如,帕金森病(PD)患者在接受 L-DOPA l-多巴治疗时,在底物(多巴胺)供应失控的情况下,该酶可能同时成为大量 ROS 生成的来源,从而进一步影响存活神经元的健康。值得一提的是,该酶在不同脑区的表达量会随着年龄的增长而增加。此外,MAO 与神经系统疾病(如帕金森病、阿尔茨海默病和抑郁症)进展的关系近来也得到了广泛研究。虽然现有的合成 MAO 抑制剂在控制这些疾病方面发挥了重要作用,但相关的并发症近来也引起了人们的极大关注。天然产品是现代药物研发中先导分子的主要来源;然而,目前仍没有一种从天然来源中提取的 MAO 抑制剂获得 FDA 批准。在这篇综述中,我们全面概述了 MAO 以及该酶系统如何参与不同年龄相关神经病理学疾病的发病机制。我们进一步讨论了长期使用现有合成 MAO 抑制剂的应用和缺点。此外,我们还强调了天然产物衍生分子在解决 MAO 相关并发症方面的前景和价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Monoamine oxidase and neurodegeneration: Mechanisms, inhibitors and natural compounds for therapeutic intervention

Mammalian flavoenzyme Monoamine oxidase (MAO) resides on the outer mitochondrial membrane (OMM) and it is involved in the metabolism of different monoamine neurotransmitters in brain. During MAO mediated oxidative deamination of relevant substrates, H2O2 is released as a catalytic by-product, thus serving as a major source of reactive oxygen species (ROS). Under normal conditions, MAO mediated ROS is reported to propel the functioning of mitochondrial electron transport chain and phasic dopamine release. However, due to its localization onto mitochondria, sudden elevation in its enzymatic activity could directly impact the form and function of the organelle. For instance, in the case of Parkinson's disease (PD) patients who are on l-dopa therapy, the enzyme could be a concurrent source of extensive ROS production in the presence of uncontrolled substrate (dopamine) availability, thus further impacting the health of surviving neurons. It is worth mentioning that the expression of the enzyme in different brain compartments increases with age. Moreover, the involvement of MAO in the progression of neurological disorders such as PD, Alzheimer's disease and depression has been extensively studied in recent times. Although the usage of available synthetic MAO inhibitors has been instrumental in managing these conditions, the associated complications have raised significant concerns lately. Natural products have served as a major source of lead molecules in modern-day drug discovery; however, there is still no FDA-approved MAO inhibitor which is derived from natural sources. In this review, we have provided a comprehensive overview of MAO and how the enzyme system is involved in the pathogenesis of different age-associated neuropathologic conditions. We further discussed the applications and drawbacks of the long-term usage of presently available synthetic MAO inhibitors. Additionally, we have highlighted the prospect and worth of natural product derived molecules in addressing MAO associated complications.

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来源期刊
Neurochemistry international
Neurochemistry international 医学-神经科学
CiteScore
8.40
自引率
2.40%
发文量
128
审稿时长
37 days
期刊介绍: Neurochemistry International is devoted to the rapid publication of outstanding original articles and timely reviews in neurochemistry. Manuscripts on a broad range of topics will be considered, including molecular and cellular neurochemistry, neuropharmacology and genetic aspects of CNS function, neuroimmunology, metabolism as well as the neurochemistry of neurological and psychiatric disorders of the CNS.
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