微rna作为阿尔茨海默病治疗的新靶点。

Behrouz Shademan, Cigir Biray Avci, Vahidreza Karamad, Fatma Sogutlu, Alireza Nourazarian
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引用次数: 1

摘要

阿尔茨海默病(AD)是最常见的与老年相关的进行性神经退行性疾病。它的特点是认知能力下降和记忆丧失,是老年人痴呆症的主要原因。阿尔茨海默病的根源可能是遗传、表观遗传或环境因素。没有药物或其他治疗药物可以预防或延缓AD的进展。MicroRNAs (miRNAs)是一种短而非编码的rna,大约可以结合200种rna。通过抑制或破坏特定的信使rna (mrna),它们控制基因表达并广泛影响细胞功能。mirna在神经系统中调控神经元生长、神经元分化、树突棘形态和突触柔韧性等方面发挥重要作用。mirna的表达水平在包括AD在内的神经系统疾病中发生改变,表明它们在疾病的发病机制中发挥重要作用。因此,靶向被破坏的mirna可能是一种新的治疗阿尔茨海默病的方法,并提供多种解决方案,包括利用β -淀粉样蛋白的有益作用,减少tau蛋白,减少神经元细胞死亡和保护阿尔茨海默病中的突触。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MicroRNAs as a New Target for Alzheimer's Disease Treatment.

Alzheimer's disease (AD) is the most common progressive neurodegenerative disease associated with advanced age. It is characterized by cognitive decline and memory loss and accounts for most cases of dementia in older people. AD can be rooted in genetic, epigenetic, or environmental causes. No drugs or other therapeutic agents prevent or delay AD progression. MicroRNAs (miRNAs) are short and uncoded RNAs that can bind to 200 RNAs approximately. By inhibiting or destroying specific messenger RNAs (mRNAs), they control gene expression and broadly affect cellular functions. MiRNAs play important roles in regulating neuronal growth, neuronal differentiation, dendritic spine morphology, and synaptic flexibility in the nervous system. The expression levels of miRNAs are changed in neurological diseases, including AD, suggesting that they play an essential role in the pathogenesis of the disease. Therefore, targeting disrupted miRNAs may be a novel therapeutic approach against AD and offers multiple solutions, including harnessing the beneficial effects of beta-amyloid, reducing tau protein, reducing neuronal cell death, and protecting synapses in AD.

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