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定量三维组织化学显示抗糖尿病药物奈格列净可使特定区域的β-淀粉样蛋白减少。

Quantitative 3D histochemistry reveals region-specific amyloid-β reduction by the antidiabetic drug netoglitazone.

作者信息

Catto Francesca, Dadgar-Kiani Ehsan, Kirschenbaum Daniel, Economides Athena, Reuss Anna Maria, Trevisan Chiara, Caredio Davide, Mirzet Delic, Frick Lukas, Weber-Stadlbauer Ulrike, Litvinov Sergey, Koumoutsakos Petros, Hyung Lee Jin, Aguzzi Adriano

机构信息

Institute of Neuropathology, University Hospital Zurich, University of Zurich, Schmelzbergstrasse 12, CH-8091 Zurich, Switzerland.

IMAI MedTech, Wagistrasse 18, 8952 Schlieren, Zurich, Switzerland.

出版信息

bioRxiv. 2024 Aug 17:2024.08.15.608042. doi: 10.1101/2024.08.15.608042.

DOI:10.1101/2024.08.15.608042
PMID:39185170
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11343181/
Abstract

A hallmark of Alzheimer's disease (AD) is the extracellular aggregation of toxic amyloid-beta (Aβ) peptides in form of plaques. Here, we identify netoglitazone, an antidiabetic compound previously tested in humans, as an Aβ aggregation antagonist. Netoglitazone improved cognition and reduced microglia activity in a mouse model of AD. Using quantitative whole-brain three-dimensional histology (Q3D), we precisely identified brain regions where netoglitazone reduced the number and size of Aβ plaques. We demonstrate the utility of Q3D in preclinical drug evaluation for AD by providing a high-resolution brain-wide view of drug efficacy. Applying Q3D has the potential to improve pre-clinical drug evaluation by providing information that can help identify mechanisms leading to brain region-specific drug efficacy.

摘要

阿尔茨海默病(AD)的一个标志是有毒的β-淀粉样蛋白(Aβ)肽以斑块形式在细胞外聚集。在此,我们确定了奈格列酮,一种先前已在人体进行测试的抗糖尿病化合物,它是一种Aβ聚集拮抗剂。在AD小鼠模型中,奈格列酮改善了认知并降低了小胶质细胞活性。使用定量全脑三维组织学(Q3D),我们精确确定了奈格列酮减少Aβ斑块数量和大小的脑区。通过提供药物疗效的全脑高分辨率视图,我们证明了Q3D在AD临床前药物评估中的效用。应用Q3D有潜力通过提供有助于确定导致脑区特异性药物疗效的机制的信息来改善临床前药物评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/926a/11343181/284535cb4c04/nihpp-2024.08.15.608042v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/926a/11343181/75a6dd3f799d/nihpp-2024.08.15.608042v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/926a/11343181/1701bc0a10c2/nihpp-2024.08.15.608042v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/926a/11343181/468be9d1fe5b/nihpp-2024.08.15.608042v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/926a/11343181/911a8f75566c/nihpp-2024.08.15.608042v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/926a/11343181/284535cb4c04/nihpp-2024.08.15.608042v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/926a/11343181/75a6dd3f799d/nihpp-2024.08.15.608042v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/926a/11343181/1701bc0a10c2/nihpp-2024.08.15.608042v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/926a/11343181/468be9d1fe5b/nihpp-2024.08.15.608042v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/926a/11343181/911a8f75566c/nihpp-2024.08.15.608042v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/926a/11343181/284535cb4c04/nihpp-2024.08.15.608042v1-f0005.jpg

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