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用于阿尔茨海默病治疗的含色酮的MTDL的Nrf2激活及抗氧化特性

Nrf2 Activation and Antioxidant Properties of Chromone-Containing MTDLs for Alzheimer's Disease Treatment.

作者信息

Simakov Alexey, Chhor Stecy, Ismaili Lhassane, Martin Hélène

机构信息

Université Marie et Louis Pasteur, INSERM UMR1322 LINC, F-25000 Besançon, France.

Université Marie et Louis Pasteur, EFS, INSERM UMR1098 RIGHT, F-25000 Besançon, France.

出版信息

Molecules. 2025 May 4;30(9):2048. doi: 10.3390/molecules30092048.

Abstract

Alzheimer's disease (AD) is a devastating neurodegenerative disorder affecting millions worldwide and imposing a significant social and economic burden. Despite extensive research, there is still no effective cure for this disease. AD is multifactorial and involves multiple etiopathogenic mechanisms, one of which is oxidative stress. Consequently, the Nrf2/ARE pathway, which regulates the expression of cellular defense genes, including those for antioxidant enzymes, is considered to be a prospective therapeutic target for AD. Meanwhile, multitarget-directed ligands (MTDLs) are a promising approach for developing effective AD medications. In this regard, we evaluated the antioxidant potential of eight chromone-containing MTDLs in vitro, including Nrf2 transcriptional activation potencies, Nrf2/ARE downstream genes activation, and antioxidant effects in vitro. All tested compounds effectively activated the Nrf2/ARE pathway. Notably, compounds , , , and demonstrated the highest Nrf2 activation potencies, while compounds , , , and significantly induced the expression of Nrf2-target antioxidant genes, specifically NQO1 and HO1. Additionally, compound exhibited a significant antioxidant effect in vitro. These findings encourage further investigation of the studied compounds, with particular emphasis on compound as the most promising candidate.

摘要

阿尔茨海默病(AD)是一种毁灭性的神经退行性疾病,影响着全球数百万人,带来了巨大的社会和经济负担。尽管进行了广泛研究,但该疾病仍无有效治愈方法。AD是多因素的,涉及多种发病机制,其中之一是氧化应激。因此,调节细胞防御基因(包括抗氧化酶基因)表达的Nrf2/ARE途径被认为是AD的一个潜在治疗靶点。同时,多靶点导向配体(MTDLs)是开发有效AD药物的一种有前景的方法。在这方面,我们在体外评估了八种含色酮的MTDLs的抗氧化潜力,包括Nrf2转录激活能力、Nrf2/ARE下游基因激活以及体外抗氧化作用。所有测试化合物均有效激活了Nrf2/ARE途径。值得注意的是,化合物 、 、 和 表现出最高的Nrf2激活能力,而化合物 、 、 和 显著诱导了Nrf2靶标抗氧化基因(特别是NQO1和HO1)的表达。此外,化合物 在体外表现出显著的抗氧化作用。这些发现鼓励对所研究的化合物进行进一步研究,尤其将化合物 作为最有前景的候选物给予特别关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2892/12074128/fd63c5d73b47/molecules-30-02048-g001.jpg

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