揭示D2AAK1及其衍生物的治疗潜力:机制见解及其在神经退行性疾病治疗中的应用

IF 4 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Michał K. Jastrzębski, Piotr Wójcik, Akanksha Mudgal, Sylwia Woźniak, Katarzyna M. Targowska-Duda, Olga Wronikowska-Denysiuk, Agnieszka Michalak, Witold Jeleniewicz, Tadeusz Karcz, Jan Raczek, Andrzej Stepulak, Agnieszka A. Kaczor
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引用次数: 0

摘要

全球预期寿命的增加伴随着神经退行性疾病的日益流行,如阿尔茨海默病(AD)。这些复杂的疾病是由多种致病因素和生物学途径引起的,需要开发多靶点的治疗策略。我们小组发现的D2AAK1由于其细胞保护、抗氧化和促进认知的特性而成为有希望的候选药物。本研究旨在进一步阐明D2AAK1及其衍生物的作用机制,重点关注它们在神经保护和认知增强方面的潜力。采用reazurin法评估D2AAK1在正常条件下和h2o2诱导氧化应激时对细胞活力的影响。通过基于细胞的ELISA检测p38 MAPK活性。采用两步定量PCR法分析mRNA表达,并通过光度、荧光和发光技术评估酶促作用。在小鼠模型上进行了行为研究,以研究化合物对记忆过程的影响。结果发现,D2AAK1及其衍生物可显著提高细胞活力,其中一些衍生物的效力高于D2AAK1。在体内,一种衍生物在新型物体识别测试中显著改善了雄性瑞士小鼠的记忆表现并逆转了东莨菪碱引起的记忆损伤。机制研究表明,D2AAK1增加了细胞保护蛋白Bcl-2和HO-1的表达,同时降低了促凋亡因子caspase-3、p38 MAPK、MAO-B的表达和活性。这些双重作用最终增强了细胞的弹性和活力,转化为改善的认知结果。这些发现表明,D2AAK1及其衍生物通过其多因素作用机制,有望作为治疗神经退行性疾病的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Unveiling the Therapeutic Potential of D2AAK1 and Its Derivatives: Mechanistic Insights and Applications in Neurodegenerative Disease Treatment

Unveiling the Therapeutic Potential of D2AAK1 and Its Derivatives: Mechanistic Insights and Applications in Neurodegenerative Disease Treatment

The global rise in life expectancy has been accompanied by a growing prevalence of neurodegenerative diseases, such as Alzheimer's disease (AD). These complex disorders arise from multiple pathogenic factors and biological pathways, necessitating the development of multi-target therapeutic strategies. D2AAK1, discovered by our group, has emerged as a promising candidate due to its cytoprotective, antioxidant, and procognitive properties. This study aimed to further elucidate the mechanisms underlying the action of D2AAK1 and its derivatives, with a focus on their potential for neuroprotection and cognitive enhancement. The effect of D2AAK1 on cell viability was evaluated under normal conditions and during H2O2-induced oxidative stress using the resazurin assay. p38 MAPK activity was measured through cell-based ELISA. mRNA expression was analyzed using a two-step quantitative PCR method, and enzymatic effects were assessed via photometric, fluorescence, and luminescence techniques. Behavioral studies in murine models were performed to investigate the influence of the compounds on memory processes. It was found that D2AAK1 and its derivatives significantly enhanced cell viability, with some derivatives exhibiting greater potency than D2AAK1. In vivo, one derivative notably improved memory performance and reversed scopolamine-induced memory impairment in the novel object recognition test in male Swiss mice. Mechanistic studies revealed that D2AAK1 increased the expression of cytoprotective proteins such as Bcl-2 and HO-1, while concurrently reducing the expression and activity of pro-apoptotic factors, including caspase-3, p38 MAPK, and MAO-B. These dual actions culminated in enhanced cellular resilience and viability, translating into improved cognitive outcomes. The findings suggest that D2AAK1 and its derivatives, through their multi-factor mechanism of action, hold promise as therapeutic agents for the treatment of neurodegenerative diseases.

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来源期刊
Journal of Neurochemistry
Journal of Neurochemistry 医学-神经科学
CiteScore
9.30
自引率
2.10%
发文量
181
审稿时长
2.2 months
期刊介绍: Journal of Neurochemistry focuses on molecular, cellular and biochemical aspects of the nervous system, the pathogenesis of neurological disorders and the development of disease specific biomarkers. It is devoted to the prompt publication of original findings of the highest scientific priority and value that provide novel mechanistic insights, represent a clear advance over previous studies and have the potential to generate exciting future research.
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