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Sirtuins 作为神经退行性和神经精神疾病的药理学靶点。

Sirtuins as pharmacological targets in neurodegenerative and neuropsychiatric disorders.

机构信息

Department of Biochemistry and Immunology, Ribeirão Preto School of Medicine, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.

Department of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.

出版信息

Br J Pharmacol. 2022 Apr;179(8):1496-1511. doi: 10.1111/bph.15570. Epub 2021 Jun 24.

Abstract

Histone deacetylases (HDACs) are enzymes that regulate several processes, such as transcription, cell proliferation, differentiation and development. HDACs are classified as either Zn -dependent or NAD -dependent enzymes. Over the years, experimental and clinical evidence has demonstrated that HDAC modulation is a critical process in neurodegenerative and psychiatric disorders. Nevertheless, most of the studies have focused on the role of Zn -dependent HDACs in the development of these diseases, although there is growing evidence showing that the NAD -dependent HDACs, known as sirtuins, are also very promising targets. This possibility has been strengthened by reports of decreased levels of NAD in CNS disorders, which can lead to alterations in sirtuin activation and therefore result in increased pathology. In this review, we discuss the role of sirtuins in neurodegenerative and neuropsychiatric disorders as well the possible rationale for them to be considered as pharmacological targets in future therapeutic interventions. LINKED ARTICLES: This article is part of a themed issue on Building Bridges in Neuropharmacology. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.8/issuetoc.

摘要

组蛋白去乙酰化酶(HDACs)是调节多种过程的酶,如转录、细胞增殖、分化和发育。HDACs 分为 Zn 依赖性或 NAD 依赖性酶。多年来,实验和临床证据表明,HDAC 调节是神经退行性和精神疾病的关键过程。然而,大多数研究都集中在 Zn 依赖性 HDACs 在这些疾病发展中的作用上,尽管越来越多的证据表明,NAD 依赖性 HDACs,即称为沉默调节蛋白,也是非常有前途的靶点。这一可能性得到了中枢神经系统疾病中 NAD 水平降低的报道的支持,这可能导致沉默调节蛋白激活的改变,从而导致病理增加。在这篇综述中,我们讨论了沉默调节蛋白在神经退行性和神经精神疾病中的作用,以及将其作为未来治疗干预的药理学靶点的可能依据。相关文章:本文是神经药理学桥梁建设专题的一部分。要查看本节中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.8/issuetoc.

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