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Cycloastragenol inhibits Aβ1–42-induced blood-brain barrier disruption and enhances soluble Aβ efflux in vitro
Journal of Asian Natural Products Research ( IF 1.7 ) Pub Date : 2020-07-01 , DOI: 10.1080/10286020.2020.1786372
Min-Ye Huang 1 , Gu-Ran Yu 1
Affiliation  

Abstract

This study aimed to evaluate the effect Cycloastragenol (CAG), a triterpenoid saponin isolated from the Radix astragali, on Aβ-induced BBB damage. An immortalized endothelial cell line (bEnd.3) was employed to mimic a BBB. The Western blot, TUNEL staining, Flow cytometric analysis and Enzyme-linked immunosorbent assay were performed. The present results showed that CAG (10, 50, 75 μM) can alleviate oligomer Aβ1–42 induced bEnd.3 cell apoptosis and increase tight junction scaffold proteins expression. The result also indicated that CAG increased soluble Aβ efflux across BBB via upregulation of the P-gp and downregulation of RAGE expression.



中文翻译:

Cycloastragenol 在体外抑制 Aβ1-42 诱导的血脑屏障破坏并增强可溶性 Aβ 流出

摘要

本研究旨在评估从黄芪中分离出的三萜皂苷环黄芪素 (CAG) 对 Aβ 诱导的 BBB 损伤的影响。使用永生化的内皮细胞系 (bEnd.3) 来模拟 BBB。进行了蛋白质印迹、TUNEL 染色、流式细胞术分析和酶联免疫吸附测定。目前的结果表明,CAG (10, 50, 75 μM) 可以减轻寡聚体 Aβ 1-42诱导的 bEnd.3 细胞凋亡并增加紧密连接支架蛋白的表达。结果还表明,CAG 通过上调 P-gp 和下调 RAGE 表达增加了穿过 BBB 的可溶性 Aβ 流出。

更新日期:2020-07-01
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