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评估和验证 作为研究阿尔茨海默病的新型体内模型。

Assessment and Validation of as a Novel In Vivo Model for Studying Alzheimer's Disease.

机构信息

Institute for Global Food Security, School of Biological Sciences, Queen's University Belfast, Belfast BT9 5DL, UK.

Biology Department, College of Science and Humanities-Al Quwaiiyah, Shaqra University, Al Quwaiiyah 19257, Saudi Arabia.

出版信息

Cells. 2021 Sep 19;10(9):2481. doi: 10.3390/cells10092481.

Abstract

BACKGROUND

Whole transgenic or non-transgenic organism model systems allow the screening of pharmacological compounds for protective actions in Alzheimer's disease (AD).

AIM

In this study, a plant parasitic nematode, , which assimilates intact peptides from the external environment, was investigated as a new potential non-transgenic model system of AD. Fresh second-stage juveniles of were used to measure their chemosensory, perform immunocytochemistry on their neurological structures, evaluate their survival rate, measure reactive oxygen species, and determine total oxidized glutathione to reduced glutathione ratio (GSSG/GSH) levels, before and after treatment with 100 µM of various amyloid beta (Aβ) peptides (1-40, 1-42, 17-42, 17-40, 1-28, or 1-16). Wild-type N2 (strain N2) was cultured on Nematode Growth Medium and directly used, as control, for chemosensory assays.

RESULTS

We demonstrated that: (i) (unlike ) assimilates amyloid-β (Aβ) peptides which co-localise with its neurological structures; (ii) pre-treatment with various Aβ isoforms (1-40, 1-42, 17-42, 17-40, 1-28, or 1-16) impairs 's chemotaxis to differing extents; (iii) Aβ peptides reduced survival, increased the production of ROS, and increased GSSG/GSH levels in this model; (iv) this unique model can distinguish differences between different treatment concentrations, durations, and modalities, displaying good sensitivity; (v) clinically approved neuroprotective agents were effective in protecting from Aβ (1-42) exposure. Taken together, the data indicate that is an interesting in vivo model with strong potential for discovery of novel bioactive compounds with anti-AD activity.

摘要

背景

全转基因或非转基因生物模型系统允许筛选阿尔茨海默病(AD)的保护作用的药物化合物。

目的

在这项研究中,一种植物寄生线虫, ,它从外部环境中吸收完整的肽,被研究为 AD 的新的潜在非转基因模型系统。新鲜的第二阶段幼虫 被用来测量它们的化学感觉,对它们的神经结构进行免疫细胞化学染色,评估它们的存活率,测量活性氧物种,并确定总氧化谷胱甘肽与还原谷胱甘肽的比值(GSSG/GSH)水平,在使用 100µM 的各种淀粉样β(Aβ)肽(1-40、1-42、17-42、17-40、1-28 或 1-16)处理前后。野生型 N2 (菌株 N2)在线虫生长培养基上培养,直接用作化学感觉测定的对照。

结果

我们证明了:(i) (与 不同)吸收淀粉样-β(Aβ)肽,其与神经结构共定位;(ii)用各种 Aβ 同工型(1-40、1-42、17-42、17-40、1-28 或 1-16)预处理在不同程度上损害了 的趋化性;(iii)Aβ 肽降低了该模型的存活率,增加了 ROS 的产生,并增加了 GSSG/GSH 水平;(iv)该独特模型能够区分不同处理浓度、持续时间和方式之间的差异,显示出良好的敏感性;(v)临床批准的神经保护剂可有效保护 免受 Aβ(1-42)暴露。综上所述,数据表明 是一种有趣的体内模型,具有发现具有抗 AD 活性的新型生物活性化合物的强大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25bf/8465914/4f6da3dfc774/cells-10-02481-g0A1.jpg

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