Suppr超能文献

野生矮丛蓝莓对大鼠全脑缺血再灌注损伤的神经保护作用:下调 iNOS/TNF-α 和上调 miR-146a/miR-21 的表达。

Neuroprotective effect of wild lowbush blueberry (Vaccinium angustifolium) on global cerebral ischemia/reperfusion injury in rats: Downregulation of iNOS/TNF-α and upregulation of miR-146a/miR-21 expression.

机构信息

Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.

Medical Plants Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.

出版信息

Phytother Res. 2021 Nov;35(11):6428-6440. doi: 10.1002/ptr.7296. Epub 2021 Sep 27.

Abstract

This study aims to investigate the neuroprotective effect of wild lowbush blueberry on CIRI in rats. Accordingly, CIRI and reperfusion were induced in rats for 60 min and 24 h, respectively. Then, the mechanisms of the neuroprotective effects of BBE were investigated in the injury through evaluating miR-146a, miR-21, and their targets in a CIRI rat model. After that, the BBE (30, 60, and 120 mg/kg b.wt) was intraperitoneally injected for 14 days, then CIRI was induced by BCCAO for 60 min for ischemic stroke and reperfusion for 24 h. Several parameters including the oxidative stress levels in the hippocampus and serum were measured 24 h after the CIRI. The findings showed that the BBE significantly decreased the levels of malondialdehyde (MDA) and nitric oxide (NO) and increased ferric ion reducing antioxidant power (FRAP) levels in the hippocampus and serum following the stroke. The BBE also maximized the miR-146a and miR-21 expressions and moderated iNOS and TNF-α expressions in the hippocampus. Likewise, the BBE enlarged the CA1 and CA3 domains of the post-stroke pyramidal cell layers of the hippocampus. Overall, the results revealed that BBE had potent neuroprotective efficacy against CIRI via the effective modulation of neuroinflammatory cascades and protected neurons against ischemic death.

摘要

本研究旨在探讨野生蓝莓对 CIRI 大鼠的神经保护作用。为此,我们分别诱导 CIRI 和再灌注 60 分钟和 24 小时。然后,通过评估 CIRI 大鼠模型中 miR-146a、miR-21 及其靶标,研究 BBE 的神经保护作用机制。之后,我们通过腹腔注射 BBE(30、60 和 120mg/kg b.wt)14 天,然后通过 BCCAO 诱导 60 分钟的脑缺血和 24 小时的再灌注来诱导 CIRI。在 CIRI 后 24 小时,测量海马体和血清中的氧化应激水平等参数。结果表明,BBE 显著降低了海马体和血清中的丙二醛(MDA)和一氧化氮(NO)水平,同时提高了铁离子还原抗氧化能力(FRAP)水平。BBE 还最大程度地提高了 miR-146a 和 miR-21 的表达,并调节了海马体中的 iNOS 和 TNF-α 的表达。此外,BBE 扩大了海马体中风后锥体细胞层的 CA1 和 CA3 区域。总之,这些结果表明,BBE 通过有效调节神经炎症级联反应对 CIRI 具有强大的神经保护作用,并保护神经元免受缺血性死亡。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验