Oregano polyphenols reduce human insulin amyloid aggregation

IF 7.5 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Biomedicine & Pharmacotherapy Pub Date : 2025-02-08 DOI:10.1016/j.biopha.2025.117904
Silvia Bittner Fialová , Miroslav Gančár , Elena Kurin , Svetlana Dokupilová , Zuzana Gažová , Milan Nagy
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Abstract

Human insulin may undergo fibrillization under specific conditions, impairing its function and promoting its accumulation in amyloid deposits. Oregano (Origanum vulgare L.) leaves are rich in biologically active compounds such as polyphenols. Thus, we investigated their ability to inhibit insulin amyloid aggregation. The oregano aqueous extract phytochemical analysis (LC-MS/MS-DAD) revealed the presence of four major compounds: lithospermic acid (LA), rosmarinic acid (RA), oreganol A (OA), and luteolin-7-O-diglucuronide (L7dG), respectively. Compounds and their mixtures were subsequently screened for anti-amyloid activity and evaluated against oregano lyophilizate (LYO) utilizing ThT assay, AFM and ATR-FTIR analyses. LYO inhibited insulin fibrillization more effectively than its main constituent RA, prolonging the lag phase approximately two-fold. L7dG has been the most effective of the tested individual compounds, prolonging the lag phase by roughly 20 %, followed by LA, whereas OA was ineffective. Subsequently, we measured the anti-amyloid activity of two kinds of equimolar mixtures: either containing individually active compounds or analogous mixtures to which inactive OA was added. Surprisingly, LA:OA mixture proved to be the most effective. However, adding L7dG to the OA mixtures led to activity loss. The interactions of oregano polyphenols with the amyloidogenic regions of insulin were elucidated using molecular docking, explaining observed changes in their anti-amyloid activity. We conclude that when investigating the anti-amyloid activity of samples of natural origin and determining the activity of the extracts and their individual main components, it is necessary to consider their mutual interactions, which can significantly affect the final effect of the analyzed mixture.
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牛至多酚可减少人胰岛素淀粉样蛋白聚集
人胰岛素可能在特定条件下发生纤化,损害其功能并促进其在淀粉样蛋白沉积物中的积累。牛至(Origanum vulgare L.)叶子富含生物活性化合物,如多酚。因此,我们研究了它们抑制胰岛素淀粉样蛋白聚集的能力。牛至水提物的植物化学分析(LC-MS/MS-DAD)结果显示,牛至水提物中存在4种主要化合物:石精酸(LA)、迷迭香酸(RA)、牛至醇A (OA)和木犀草素-7- o -二lucuronide (L7dG)。随后对化合物及其混合物进行抗淀粉样蛋白活性筛选,并利用ThT试验、AFM和ATR-FTIR分析对牛至冻干液(LYO)进行抗淀粉样蛋白活性评估。LYO比其主要成分RA更有效地抑制胰岛素纤维化,延迟期延长约两倍。L7dG是测试的单个化合物中最有效的,延迟期延长了大约20% %,其次是LA,而OA无效。随后,我们测量了两种等摩尔混合物的抗淀粉样蛋白活性:含有单独活性化合物或添加无活性OA的类似混合物。令人惊讶的是,LA:OA混合物被证明是最有效的。然而,在OA混合物中加入L7dG会导致活性损失。牛至多酚与胰岛素淀粉样蛋白区相互作用的分子对接被阐明,解释了观察到的抗淀粉样蛋白活性的变化。我们得出结论,在研究天然来源样品的抗淀粉样蛋白活性和确定提取物及其单个主要成分的活性时,有必要考虑它们之间的相互作用,这将显著影响所分析混合物的最终效果。
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来源期刊
CiteScore
11.90
自引率
2.70%
发文量
1621
审稿时长
48 days
期刊介绍: Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.
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