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缺氧和化学预处理在亨廷顿病中的作用机制。

A Rationale for Hypoxic and Chemical Conditioning in Huntington's Disease.

机构信息

Department of Biomedical Sciences, University of Lausanne, 1015 Lausanne, Switzerland.

Institute of Sport Sciences, University of Lausanne, 1015 Lausanne, Switzerland.

出版信息

Int J Mol Sci. 2021 Jan 8;22(2):582. doi: 10.3390/ijms22020582.

Abstract

Neurodegenerative diseases are characterized by adverse cellular environments and pathological alterations causing neurodegeneration in distinct brain regions. This development is triggered or facilitated by conditions such as hypoxia, ischemia or inflammation and is associated with disruptions of fundamental cellular functions, including metabolic and ion homeostasis. Targeting intracellular downstream consequences to specifically reverse these pathological changes proved difficult to translate to clinical settings. Here, we discuss the potential of more holistic approaches with the purpose to re-establish a healthy cellular environment and to promote cellular resilience. We review the involvement of important molecular pathways (e.g., the sphingosine, δ-opioid receptor or N-Methyl-D-aspartate (NMDA) receptor pathways) in neuroprotective hypoxic conditioning effects and how these pathways can be targeted for chemical conditioning. Despite the present scarcity of knowledge on the efficacy of such approaches in neurodegeneration, the specific characteristics of Huntington's disease may make it particularly amenable for such conditioning techniques. Not only do classical features of neurodegenerative diseases like mitochondrial dysfunction, oxidative stress and inflammation support this assumption, but also specific Huntington's disease characteristics: a relatively young age of neurodegeneration, molecular overlap of related pathologies with hypoxic adaptations and sensitivity to brain hypoxia. The aim of this review is to discuss several molecular pathways in relation to hypoxic adaptations that have potential as drug targets in neurodegenerative diseases. We will extract the relevance for Huntington's disease from this knowledge base.

摘要

神经退行性疾病的特征是不良的细胞环境和病理性改变导致特定脑区的神经退行性变。这种发展是由缺氧、缺血或炎症等条件引发或促进的,并与基本细胞功能的紊乱有关,包括代谢和离子平衡。针对细胞内下游后果的靶向治疗以特异性逆转这些病理变化,被证明难以转化为临床应用。在这里,我们讨论了更全面的方法的潜力,目的是重建健康的细胞环境和促进细胞的弹性。我们回顾了重要分子途径(例如,鞘氨醇、δ-阿片受体或 N-甲基-D-天冬氨酸(NMDA)受体途径)在神经保护缺氧预处理效应中的作用,以及如何针对这些途径进行化学预处理。尽管目前对这些方法在神经退行性变中的疗效知之甚少,但亨廷顿病的特定特征可能使其特别适合这种条件技术。不仅神经退行性疾病的典型特征,如线粒体功能障碍、氧化应激和炎症支持这一假设,而且亨廷顿病的特定特征也是如此:神经退行性变的相对年轻、与缺氧适应相关的相关病理学的分子重叠以及对脑缺氧的敏感性。本综述的目的是讨论与缺氧适应相关的几种分子途径,这些途径有可能成为神经退行性疾病的药物靶点。我们将从这一知识库中提取出与亨廷顿病相关的内容。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b84/7826574/a2bfabb89399/ijms-22-00582-g001.jpg

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