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川陈皮素通过抑制神经炎症和氧化/硝化应激来预防淀粉样β诱导的认知障碍。

Nobiletin prevents amyloid β-induced cognitive impairment via inhibition of neuroinflammation and oxidative/nitrosative stress.

机构信息

Department of Physiology, School of Medicine, Shahed University, Tehran, Iran.

Neurophysiology Research Center, Department of Physiology, Shahed University, Tehran, Iran.

出版信息

Metab Brain Dis. 2022 Jun;37(5):1337-1349. doi: 10.1007/s11011-022-00949-y. Epub 2022 Mar 16.

Abstract

Alzheimer's disease (AD) is presented as an age-related neurodegenerative disease with multiple cognitive deficits and amyloid β (Aβ) accumulation is the most important involved factor in its development. Nobiletin is a bioflavonoid isolated from citrus fruits peels with anti-inflammatory and anti-oxidative activity as well as anti-dementia property that has shown potency to ameliorate intracellular and extracellular Ab. The aim of the present study was to assess protective effect of nobiletin against Aβ-induced cognitive impairment as a consistent model of AD. After bilateral intrahippocampal (CA1 subfield) injection of Aβ, rats were treated with nobiletin (10 mg/kg/day; p.o.) from stereotaxic surgery day (day 0) till day + 7. Cognition function was evaluated in a battery of behavioral tasks at week 3 with final assessment of hippocampal oxidative stress and inflammation besides Nissl staining and 3-nitrotyrosine (3-NT) immunohistochemistry. Analysis of behavioral data showed notable and significant improvement of alternation in Y maze test, discrimination ratio in novel object recognition task, and step through latency in passive avoidance test in nobiletin-treated Aβ group. Additionally, nobiletin treatment was associated with lower hippocampal levels of MDA and ROS and partial reversal of SOD activity and also improvement of Nrf2 with no significant effect on GSH and catalase. Furthermore, nobiletin attenuated hippocampal neuroinflammation in Aβ group as shown by lower tissue levels of TLR4, NF-kB, and TNFa. Histochemical findings showed that nobiletin prevents CA1 neuronal loss in Nissl staining in addition to its alleviation of 3-nitrotyrosine (3-NT) immunoreactivity as a marker of nitrosative stress. Collectively, these findings indicated neuroprotective and anti-dementia potential of nobiletin that is partly attributed to its anti-oxidative, anti-nitrosative, and anti-inflammatory property associated with proper modulation of TLR4/NF-kB/Nrf2 pathways.

摘要

阿尔茨海默病(AD)是一种与年龄相关的神经退行性疾病,具有多种认知缺陷,淀粉样β(Aβ)积累是其发展过程中最重要的相关因素。诺比汀是一种从柑橘类水果果皮中分离出来的生物类黄酮,具有抗炎和抗氧化活性以及抗痴呆特性,已显示出改善细胞内和细胞外 Ab 的能力。本研究旨在评估诺比汀对 Aβ 诱导的认知障碍的保护作用,作为 AD 的一致模型。在双侧海马(CA1 亚区)内注射 Aβ 后,从立体定向手术日(第 0 天)到第+7 天,用诺比汀(10mg/kg/天;po)治疗大鼠。在第 3 周通过一系列行为任务评估认知功能,最终评估海马氧化应激和炎症,以及尼氏染色和 3-硝基酪氨酸(3-NT)免疫组织化学。行为数据分析显示,在 Y 迷宫试验中交替、新物体识别任务中的辨别率以及被动回避试验中的潜伏期显著改善,在诺比汀处理的 Aβ组中。此外,诺比汀治疗与海马 MDA 和 ROS 水平降低以及 SOD 活性部分逆转有关,同时改善 Nrf2,对 GSH 和过氧化氢酶无显著影响。此外,诺比汀可减轻 Aβ组海马神经炎症,表现为 TLR4、NF-kB 和 TNFa 的组织水平降低。组织化学发现,诺比汀可防止 Nissl 染色中的 CA1 神经元丢失,并减轻 3-硝基酪氨酸(3-NT)免疫反应性作为硝化应激的标志物。总之,这些发现表明诺比汀具有神经保护和抗痴呆潜力,部分归因于其抗氧化、抗硝化和抗炎特性,以及适当调节 TLR4/NF-kB/Nrf2 途径。

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