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亚精胺作为神经退行性疾病中自噬的表观遗传调节剂。

Spermidine as an epigenetic regulator of autophagy in neurodegenerative disorders.

机构信息

Department of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.

Department of Pharmaceutical Biotechnology, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.

出版信息

Eur J Pharmacol. 2024 Sep 15;979:176823. doi: 10.1016/j.ejphar.2024.176823. Epub 2024 Jul 18.

Abstract

Autophagy is an abnormal protein degradation and recycling process that is impaired in various neurological diseases like Alzheimer's disease (AD), Parkinson's disease (PD), and Huntington's disease. Spermidine is a natural polyamine found in various plant- and meat-based diets that can induce autophagy, and is decreased in various neurodegenerative diseases. It acts on epigenetic enzymes like E1A-binding protein p300, HAT enzymes like Iki3p and Sas3p, and α-tubulin acetyltransferase 1 that modulate autophagy. Histone modifications like acetylation, phosphorylation, and methylation could influence autophagy. Autophagy is epigenetically regulated in various neurodegenerative disorders with many epigenetic enzymes and miRNAs. Polyamine regulation plays an essential role in the disease pathogenesis of AD and PD. Therefore, in this review, we discuss various enzymes and miRNAs involved in the epigenetic regulation of autophagy in neurodegenerative disorders and the role of spermidine as an autophagy enhancer. The alterations in spermidine-mediated regulation of Beclin-1, LC3-II, and p62 genes in AD and other PD-associated enzymes could impact the process of autophagy in these neurodegenerative diseases. With the ever-growing data and such promising effects of spermidine in autophagy, we feel it could be a promising target in this area and worth further detailed studies.

摘要

自噬是一种异常的蛋白质降解和回收过程,在各种神经退行性疾病中受到损害,如阿尔茨海默病(AD)、帕金森病(PD)和亨廷顿病。亚精胺是一种存在于各种植物和肉类饮食中的天然多胺,可以诱导自噬,并且在各种神经退行性疾病中减少。它作用于表观遗传酶,如 E1A 结合蛋白 p300、HAT 酶如 Iki3p 和 Sas3p,以及调节自噬的α-微管蛋白乙酰转移酶 1。组蛋白修饰,如乙酰化、磷酸化和甲基化,可能影响自噬。自噬在多种神经退行性疾病中受到表观遗传调控,涉及许多表观遗传酶和 miRNA。多胺调节在 AD 和 PD 的疾病发病机制中起着至关重要的作用。因此,在这篇综述中,我们讨论了参与神经退行性疾病中自噬的表观遗传调控的各种酶和 miRNA,以及亚精胺作为自噬增强剂的作用。AD 和其他 PD 相关酶中 Beclin-1、LC3-II 和 p62 基因的亚精胺介导调节的改变可能会影响这些神经退行性疾病中自噬的过程。随着越来越多的数据和亚精胺在自噬中的这种有希望的效果,我们认为它可能是该领域的一个有前途的靶点,值得进一步详细研究。

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