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无细胞和体内鉴定可可黄烷醇对共济失调蛋白 Ataxin-3 的抑制活性:针对脊髓小脑共济失调 3 型的新方法。

Cell-Free and In Vivo Characterization of the Inhibitory Activity of Cocoa Flavanols on the Amyloid Protein Ataxin-3: Toward New Approaches against Spinocerebellar Ataxia Type 3.

机构信息

Department of Biotechnology and Biosciences, University of Milano-Bicocca, P.zza Della Scienza 2, 20126 Milan, Italy.

NeuroMI, Milan Center for Neuroscience, University of Milano-Bicocca, 20126 Milano, Italy.

出版信息

ACS Chem Neurosci. 2024 Jan 17;15(2):278-289. doi: 10.1021/acschemneuro.3c00560. Epub 2023 Dec 28.


DOI:10.1021/acschemneuro.3c00560
PMID:38154144
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10797631/
Abstract

Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder characterized by ataxia and other neurological manifestations, with a poor prognosis and a lack of effective therapies. The amyloid aggregation of the ataxin-3 protein is a hallmark of SCA3 and one of the main biochemical events prompting its onset, making it a prominent target for the development of preventive and therapeutic interventions. Here, we tested the efficacy of an aqueous cocoa extract and its polyphenolic components against ataxin-3 aggregation and neurotoxicity. The combination of biochemical assays and atomic force microscopy morphological analysis provided clear evidence of cocoa flavanols' ability to hinder ATX3 amyloid aggregation through direct physical interaction, as assessed by NMR spectroscopy. The chemical identity of the flavanols was investigated by ultraperformance liquid chromatography-high-resolution mass spectrometry. The use of the preclinical model allowed us to demonstrate cocoa flavanols' ability to ameliorate ataxic phenotypes in vivo. To the best of our knowledge, cocoa is the first natural source whose extract is able to directly interfere with ATX3 aggregation, leading to the formation of off-pathway species.

摘要

脊髓小脑共济失调 3 型(SCA3)是一种以共济失调和其他神经表现为特征的神经退行性疾病,预后不良,缺乏有效治疗方法。ataxin-3 蛋白的淀粉样聚集是 SCA3 的标志之一,也是促使其发病的主要生化事件之一,使其成为预防和治疗干预的重要靶点。在这里,我们测试了一种水性可可提取物及其多酚成分对 ataxin-3 聚集和神经毒性的疗效。生化分析和原子力显微镜形态分析的结合提供了明确的证据,表明可可黄烷醇能够通过直接物理相互作用阻止 ATX3 淀粉样聚集,这一点通过 NMR 光谱得到了评估。黄烷醇的化学性质通过超高效液相色谱-高分辨率质谱进行了研究。使用临床前模型,我们能够证明可可黄烷醇能够改善体内的共济失调表型。据我们所知,可可提取物是第一种能够直接干扰 ATX3 聚集、形成非通路物种的天然来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/b08ba4bf55b9/cn3c00560_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/c2c202796d6c/cn3c00560_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/a5618055b49a/cn3c00560_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/c51ae458e007/cn3c00560_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/19b8a5a372e1/cn3c00560_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/44491eeaf590/cn3c00560_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/b08ba4bf55b9/cn3c00560_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/c2c202796d6c/cn3c00560_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/a5618055b49a/cn3c00560_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/c51ae458e007/cn3c00560_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/19b8a5a372e1/cn3c00560_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/44491eeaf590/cn3c00560_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0bb/10797631/b08ba4bf55b9/cn3c00560_0006.jpg

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引用本文的文献

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Dietary and lifestyle interventions for the management of hereditary ataxias.

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本文引用的文献

[1]
Alzheimer's Disease Prevention through Natural Compounds: Cell-Free, and Dissection of Hop ( L.) Multitarget Activity.

ACS Chem Neurosci. 2022-11-16

[2]
NMR-Driven Identification of Cinnamon Bud and Bark Components With Anti-Aβ Activity.

Front Chem. 2022-6-8

[3]
Oxidative Stress and Neurodegeneration: Interconnected Processes in PolyQ Diseases.

Antioxidants (Basel). 2021-9-13

[4]
NMR-based Lavado cocoa chemical characterization and comparison with fermented cocoa varieties: Insights on cocoa's anti-amyloidogenic activity.

Food Chem. 2020-10-1

[5]
Identifying Therapeutic Targets for Spinocerebellar Ataxia Type 3/Machado-Joseph Disease through Integration of Pathological Biomarkers and Therapeutic Strategies.

Int J Mol Sci. 2020-4-26

[6]
On-cell saturation transfer difference NMR study of Bombesin binding to GRP receptor.

Bioorg Chem. 2020-6

[7]
Revisiting thioflavin T (ThT) fluorescence as a marker of protein fibrillation - The prominent role of electrostatic interactions.

J Colloid Interface Sci. 2020-8-1

[8]
Pathogenesis of SCA3 and implications for other polyglutamine diseases.

Neurobiol Dis. 2020-2

[9]
Methacycline displays a strong efficacy in reducing toxicity in a SCA3 Caenorhabditis elegans model.

Biochim Biophys Acta Gen Subj. 2018-10-27

[10]
bioNMR-based identification of natural anti-Aβ compounds in Peucedanum ostruthium.

Bioorg Chem. 2018-10-12

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