Sirtuin-1 在阿尔茨海默病中的潜在作用:回顾生物和环境证据

IF 2.8 Q2 NEUROSCIENCES
Journal of Alzheimer's disease reports Pub Date : 2023-08-04 eCollection Date: 2023-01-01 DOI:10.3233/ADR-220088
Mehrane Mehramiz, Tenielle Porter, Eleanor K O'Brien, Stephanie R Rainey-Smith, Simon M Laws
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引用次数: 0

摘要

由 SIRT1 基因编码的 Sirtuin-1(Sirt1)是一种保守的烟酰胺腺嘌呤二核苷酸(NAD+)依赖性去乙酰化酶,被认为是人类新陈代谢的主调节器。Sirt1 受饮食和运动等生活方式的影响,通过多种机制对多种生物通路做出贡献。健康生活方式的重要性与阿尔茨海默病(AD)等高发的现代慢性疾病息息相关。越来越多的证据表明,Sirt1/SIRT1 在阿尔茨海默病的病理机制中发挥着多层次的作用。因此,本综述将通过 Sirt1/SIRT1 对淀粉样蛋白-β 新陈代谢和磷酸化 tau 降解的影响,描述 Sirt1/SIRT1 参与阿尔茨海默病病理特征发展的情况,从而探讨 Sirt1 与阿尔茨海默病病理机制的相关性。然后,我们探讨了 Sirt1/SIRT1 在不同的 AD 相关生物过程中的参与,包括胆固醇代谢、炎症、昼夜节律和肠道微生物组,最后讨论了 Sirt1 与 AD 相关生活方式因素(如饮食、体育锻炼和吸烟)以及常见合并症抑郁症之间的相互作用。全基因组关联研究探讨了 SIRT1 与注意力缺失症以及注意力缺失症风险因素和并发症之间的潜在关联。我们从基因层面总结了这些证据,以强调 SIRT1 与注意力缺失症之间的联系,尤其是与注意力缺失症相关风险因素(如心脏病)的联系。最后,我们回顾了目前有关 SIRT1 基因变异与生活方式因素之间潜在相互作用的文献,以及这些证据如何支持了进一步研究的必要性,以确定这些相互作用与注意力缺失症和痴呆症的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Potential Role for Sirtuin-1 in Alzheimer's Disease: Reviewing the Biological and Environmental Evidence.

A Potential Role for Sirtuin-1 in Alzheimer's Disease: Reviewing the Biological and Environmental Evidence.

A Potential Role for Sirtuin-1 in Alzheimer's Disease: Reviewing the Biological and Environmental Evidence.

Sirtuin-1 (Sirt1), encoded by the SIRT1 gene, is a conserved Nicotinamide adenine dinucleotide (NAD+) dependent deacetylase enzyme, considered as the master regulator of metabolism in humans. Sirt1 contributes to a wide range of biological pathways via several mechanisms influenced by lifestyle, such as diet and exercise. The importance of a healthy lifestyle is of relevance to highly prevalent modern chronic diseases, such as Alzheimer's disease (AD). There is growing evidence at multiple levels for a role of Sirt1/SIRT1 in AD pathological mechanisms. As such, this review will explore the relevance of Sirt1 to AD pathological mechanisms, by describing the involvement of Sirt1/SIRT1 in the development of AD pathological hallmarks, through its impact on the metabolism of amyloid-β and degradation of phosphorylated tau. We then explore the involvement of Sirt1/SIRT1 across different AD-relevant biological processes, including cholesterol metabolism, inflammation, circadian rhythm, and gut microbiome, before discussing the interplay between Sirt1 and AD-related lifestyle factors, such as diet, physical activity, and smoking, as well as depression, a common comorbidity. Genome-wide association studies have explored potential associations between SIRT1 and AD, as well as AD risk factors and co-morbidities. We summarize this evidence at the genetic level to highlight links between SIRT1 and AD, particularly associations with AD-related risk factors, such as heart disease. Finally, we review the current literature of potential interactions between SIRT1 genetic variants and lifestyle factors and how this evidence supports the need for further research to determine the relevance of these interactions with respect to AD and dementia.

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