Activation of NF-κB Signal Pathway and Downstream IL-1β Expression in Hippocampal Astrocytes of LPS-Induced Aged Rats

Kan Min-Hui, Fu Hui-qun, F. Long, W. Yan, Wang Tian-long
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Abstract

Background: The activation of nuclear factor-kappa B (NF-κB) signal pathway and downstream expression of IL-1β may play a pivotal role in neuroinflammation and cognitive dysfunction. We previously reported that a single lipopolysaccharide (LPS) dose induces prolonged neuroinflammation which is associated with astrocytic NF-κB signal pathways in aged rats. Blockade of the pathway by pyrrolidine dithiocarbamate (PDTC) in astrocytes could markedly suppress them, which may provide innovative ideas for clinical improvement for postoperative cognitive dysfunction (POCD). Methods: Rats were randomly assigned to vehicle, LPS, LPS+PDTC groups (n = 8 per group, per time point). 1) vehicle control (0.9% NaCl i.p.), 2) LPS (2 mg/kg i.p), 3) LPS + PDTC (LPS and PDTC50 mg/kg i.p.). After injection, whole brain tissues acquired at a series of time points (days 1, 3,7, 15 and 30) was prepared to carry out immunofluorescence, isolated hippocampal tissues were used for enzyme-linked immunosorbent assay (ELISA). NF-κB p65, p-IκBα and IL-1β were detected respectively by immunofluorescence and IL-1β protein levels were determined by ELISA. A separate cohort of rats (n=8-10/group) were tested in a Morris water maze (MWM) for spatial learning and memory. Results: The PDTC treatment suppressed the LPS-induced canonical NF-κB signaling pathway- nuclear translocation of NF-κB p65 and IκBα phosphorylation, positive expression of GFAP and IL-1β in hippocampal astrocytes of aged rats by immunofluorescence and reduced cognitive dysfunction by MWM test; The LPS-induced IL-1β protein increase in hippocampus of aged rats was attenuated by PDTC with ELISA. Conclusion: These findings suggest that NF-κB signaling pathway and downstream IL-1β in senescent astrocytes may play important roles in age-related neuroinflammation and cognitive dysfunction and provide potential discovery tool and therapeutic methods with PDTC for verifying the NF-κB signal pathway and treating cognitive impairment, especially POCD. (Funded by National Clinical Research for Geriatric Disorders of China, and Beijing Municipal Administration of Hospitals' Ascent Plan.)     Citation: Min-Hui Kan, Hui-Qun Fu, Long Fan, Yan Wu, Tian-Long Wang. Activation of NF-κB Signal Pathway and Downstream IL-1β Expression in Hippocampal Astrocytes of LPS-Induced Aged Rats. J Anesth Perioper Med 2017; 4 : 149-61. doi: 10.24015/ JAPM.2017.0051 This is an open-access article, published by Evidence Based Communications (EBC). This work is licensed under the Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution, and reproduction in any medium or format for any lawful purpose. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
脂多糖诱导衰老大鼠海马星形胶质细胞NF-κB信号通路激活及下游IL-1β表达
背景:核因子κB (NF-κB)信号通路的激活和IL-1β的下游表达可能在神经炎症和认知功能障碍中起关键作用。我们之前报道过单次脂多糖(LPS)剂量可诱导老年大鼠延长神经炎症,这与星形细胞NF-κB信号通路有关。利用二硫代氨基甲酸吡咯烷酯(PDTC)阻断星形胶质细胞的这一通路可显著抑制星形胶质细胞的凋亡,这可能为临床改善术后认知功能障碍(POCD)提供创新思路。方法:将大鼠随机分为载药组、LPS组、LPS+PDTC组(每组8只,每个时间点)。1)对照(0.9% NaCl i.p), 2) LPS (2 mg/kg i.p), 3) LPS + PDTC (LPS和PDTC50 mg/kg i.p)。注射后,取1、3、7、15、30天的全脑组织进行免疫荧光检测,分离海马组织进行酶联免疫吸附试验(ELISA)。免疫荧光法检测各组小鼠NF-κB p65、p -κB α、IL-1β蛋白水平,ELISA法检测各组小鼠IL-1β蛋白水平。采用Morris水迷宫(Morris water maze, MWM)测试大鼠空间学习记忆能力,每组8-10只。结果:经免疫荧光检测,PDTC可抑制lps诱导的典型NF-κ b信号通路- NF-κ b p65核易位和i -κ b α磷酸化,抑制衰老大鼠海马星形胶质细胞GFAP和IL-1β的阳性表达,MWM检测可减轻认知功能障碍;ELISA法观察PDTC对lps诱导的老年大鼠海马组织IL-1β蛋白升高的影响。结论:上述发现提示衰老星形胶质细胞中NF-κB信号通路及其下游IL-1β可能在年龄相关性神经炎症和认知功能障碍中发挥重要作用,为验证NF-κB信号通路,治疗认知功能障碍,特别是POCD提供了潜在的发现工具和治疗方法。(国家老年病临床研究、北京市医院管理局提升计划资助)引用本文:阚敏慧,傅惠群,范龙,吴燕,王天龙。脂多糖诱导衰老大鼠海马星形胶质细胞NF-κB信号通路激活及下游IL-1β表达中华外科杂志2017;[4]: 149-61。doi: 10.24015/ JAPM.2017.0051这是一篇开放获取的文章,由Evidence Based Communications (EBC)发表。本作品遵循知识共享署名4.0国际许可协议,允许以任何媒介或格式出于任何合法目的不受限制地使用、分发和复制。要查看此许可证的副本,请访问http://creativecommons.org/licenses/by/4.0/。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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