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非瑟酮作为衰老治疗药物的蓝本——用分子模型阐明其老年保护和衰老细胞溶解特性

Fisetin as a Blueprint for Senotherapeutic Agents - Elucidating Geroprotective and Senolytic Properties with Molecular Modeling.

作者信息

Spiegel Maciej

机构信息

Department of Organic Chemistry and Pharmaceutical Technology, Faculty of Pharmacy, Wroclaw Medical University, Borowska 211A, 50-556, Wroclaw, Poland.

出版信息

Chemistry. 2025 Mar 17;31(16):e202403755. doi: 10.1002/chem.202403755. Epub 2025 Jan 28.

Abstract

Targeting senescent cells and the factors that accelerate this pathological state has recently emerged as a novel field in medicinal chemistry. As attention shifts to synthetic substances, studies on natural agents are often overlooked. In this paper, we present a detailed computational modeling study that encompasses quantum mechanics and molecular dynamics to elucidate the senotherapeutic activity of fisetin, a natural flavonoid. The mitochondrial environment, serving as a proxy for senescence, received special attention. Throughout the study, fisetin's outstanding geroprotective properties-exhibiting significant potential against ⋅OOH, O⋅, and ⋅OH radicals, surpassing those of Trolox or ascorbate-were identified. Furthermore, fisetin demonstrated a high capacity to restore oxidatively damaged biomolecules to their pristine forms, thereby renewing the functionality of proteins and amino acids. The senolytic properties were examined in terms of Bcl-2 and Bcl-xL inhibition. The results indicated that fisetin not only binds effectively to these proteins but also, with appropriate modifications, may exhibit specific selectivity toward either target. This study highlights fisetin's remarkable activity in these areas and provides a molecular description of the underlying processes, paving the way for future research.

摘要

靶向衰老细胞以及加速这种病理状态的因素,最近已成为药物化学领域的一个新方向。随着研究重点转向合成物质,对天然药物的研究常常被忽视。在本文中,我们开展了一项详细的计算建模研究,该研究涵盖量子力学和分子动力学,以阐明天然黄酮类化合物非瑟酮的衰老治疗活性。作为衰老替代指标的线粒体环境受到了特别关注。在整个研究过程中,我们发现非瑟酮具有出色的老年保护特性,对·OOH、O·和·OH自由基具有显著的对抗潜力,超过了生育三烯酚或抗坏血酸。此外,非瑟酮具有强大的能力,能将氧化损伤的生物分子恢复到原始状态,从而恢复蛋白质和氨基酸的功能。我们从抑制Bcl - 2和Bcl - xL的角度研究了非瑟酮的溶酶体特性。结果表明,非瑟酮不仅能有效地与这些蛋白质结合,而且经过适当修饰后,可能对任一靶点表现出特定的选择性。本研究突出了非瑟酮在这些领域的显著活性,并提供了潜在过程的分子描述,为未来的研究铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73dd/11914956/a2b6344dc3b9/CHEM-31-e202403755-g008.jpg

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