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氧化应激与神经退行性变:多聚谷氨酰胺疾病中的相互关联过程。

Oxidative Stress and Neurodegeneration: Interconnected Processes in PolyQ Diseases.

作者信息

Gkekas Ioannis, Gioran Anna, Boziki Marina Kleopatra, Grigoriadis Nikolaos, Chondrogianni Niki, Petrakis Spyros

机构信息

Institute of Applied Biosciences/Centre for Research and Technology Hellas, 57001 Thessaloniki, Greece.

Institute of Chemical Biology, National Hellenic Research Foundation, 11635 Athens, Greece.

出版信息

Antioxidants (Basel). 2021 Sep 13;10(9):1450. doi: 10.3390/antiox10091450.

Abstract

Neurodegenerative polyglutamine (polyQ) disorders are caused by trinucleotide repeat expansions within the coding region of disease-causing genes. PolyQ-expanded proteins undergo conformational changes leading to the formation of protein inclusions which are associated with selective neuronal degeneration. Several lines of evidence indicate that these mutant proteins are associated with oxidative stress, proteasome impairment and microglia activation. These events may correlate with the induction of inflammation in the nervous system and disease progression. Here, we review the effect of polyQ-induced oxidative stress in cellular and animal models of polyQ diseases. Furthermore, we discuss the interplay between oxidative stress, neurodegeneration and neuroinflammation using as an example the well-known neuroinflammatory disease, Multiple Sclerosis. Finally, we review some of the pharmaceutical interventions which may delay the onset and progression of polyQ disorders by targeting disease-associated mechanisms.

摘要

神经退行性多聚谷氨酰胺(polyQ)疾病是由致病基因编码区内的三核苷酸重复扩增引起的。多聚谷氨酰胺扩展的蛋白质会发生构象变化,导致形成与选择性神经元变性相关的蛋白质内含物。多项证据表明,这些突变蛋白与氧化应激、蛋白酶体损伤和小胶质细胞活化有关。这些事件可能与神经系统炎症的诱导和疾病进展相关。在此,我们综述了多聚谷氨酰胺诱导的氧化应激在多聚谷氨酰胺疾病细胞和动物模型中的作用。此外,我们以著名的神经炎症性疾病多发性硬化症为例,讨论氧化应激、神经退行性变和神经炎症之间的相互作用。最后,我们综述了一些可能通过靶向疾病相关机制来延缓多聚谷氨酰胺疾病发病和进展的药物干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7213/8471619/54356e891a72/antioxidants-10-01450-g001.jpg

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