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姜黄素通过调节大脑中的氧化应激和 ERK1/2/NF-B 通路逆转地西泮引起的认知障碍。

Curcumin Reverses the Diazepam-Induced Cognitive Impairment by Modulation of Oxidative Stress and ERK 1/2/NF-B Pathway in Brain.

机构信息

Department of Physiology, "Iuliu Hatieganu" University of Medicine and Pharmacy, 1 Clinicilor Street, 400006 Cluj-Napoca, Romania.

Department of Molecular Biology and Biotechnology, Faculty of Biology and Geology, Babes-Bolyai University, Clinicilor Street No. 5-7, Cluj-Napoca, Romania.

出版信息

Oxid Med Cell Longev. 2017;2017:3037876. doi: 10.1155/2017/3037876. Epub 2017 Oct 2.

DOI:10.1155/2017/3037876
PMID:29098059
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5643119/
Abstract

Oxidative stress and inflammation can be involved in cognitive dysfunction associated with neurodegenerative disorders. Diazepam (DZP) administration has been chosen to simulate the memory impairment. The aim of this study was to evaluate the effects of curcumin (CUR) on spatial cognition, ambulatory activity, and blood and brain oxidative stress levels. The ERK/NF-B signaling pathway and the histopathological changes in the hippocampus and frontal lobe, in diazepam-treated rats, were also analyzed. The animals were divided into 4 groups: control, carboxymethylcellulose (CMC) + CUR, CMC + DZP, and CUR + CMC + DZP. CUR (150 mg/kg b.w.) was orally administered for 28 days. DZP (2 mg/kg b.w.) was intraperitoneally administered 20 minutes before the behavioral tests (open field test, Y-maze, and elevated plus maze). CUR improved the spontaneous alternation behavior, decreased the oxidative stress levels, both in the blood and in the hippocampus, and downregulated the extracellular signal-regulated kinase (ERK 1/2)/nuclear transcription factor- (NF-) B/pNF-B pathway in the hippocampus and the iNOS expression in the hippocampus and frontal lobe of the DZP-treated rats. Histopathologically, no microscopic changes were found. The immunohistochemical signal of iNOS decreased in the DZP and CUR-treated group. Thus, our findings suggest that curcumin administration may improve the cognitive performance and may also have an antioxidant effect.

摘要

氧化应激和炎症可能与神经退行性疾病相关的认知功能障碍有关。地西泮(DZP)的给药已被选择用于模拟记忆障碍。本研究旨在评估姜黄素(CUR)对空间认知、活动能力以及血液和大脑氧化应激水平的影响。还分析了 DZP 处理大鼠 ERK/NF-B 信号通路和海马体和额叶的组织病理学变化。动物分为 4 组:对照组、羧甲基纤维素(CMC)+CUR、CMC+DZP 和 CUR+CMC+DZP。CUR(150mg/kg b.w.)口服给药 28 天。DZP(2mg/kg b.w.)在行为测试(旷场试验、Y 迷宫和高架十字迷宫)前 20 分钟腹腔注射。CUR 改善了自发交替行为,降低了氧化应激水平,无论是在血液中还是在海马体中,并且下调了海马体中的细胞外信号调节激酶(ERK 1/2)/核转录因子-(NF)-B/pNF-B 通路和 DZP 处理大鼠海马体和额叶中的诱导型一氧化氮合酶(iNOS)表达。组织病理学上未发现微观变化。DZP 和 CUR 处理组的 iNOS 免疫组化信号降低。因此,我们的研究结果表明,姜黄素给药可能改善认知表现,并且还可能具有抗氧化作用。

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