SIRT1通过TLR4/NF-κB通路介导心脏外科术后认知功能障碍的改善

Jing Shi, X. Zou, Ke Jiang, Feng Wang
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引用次数: 23

摘要

摘要目的临床上对术后认知功能障碍(POCD)尚无有效的治疗方法。术后炎症与POCD密切相关。方法本研究探讨sirtuin 1 (SIRT1)在POCD中的作用。心脏手术诱导小鼠POCD。实时聚合酶链反应(real-time polymerase chain reaction)和western blot检测相关基因mRNA和蛋白表达水平。采用ELISA试剂盒检测血浆炎症因子浓度。进行了新的目标和新的位置识别测试,以衡量识别能力。采用Morris水迷宫(MWM)测试学习记忆能力。结果POCD后SIRT1表达明显降低。SIRT1激活物SRT1720促进POCD小鼠的识别、学习和记忆能力。此外,SRT1720处理可显著抑制POCD小鼠血浆炎症细胞因子水平和海马TLR4和P65蛋白表达。SRT1720对POCD的作用依赖于tlr4。结论SIRT1通过TLR4/NF-κB通路介导心脏手术术后认知功能障碍的改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SIRT1 mediates improvement of cardiac surgery-induced postoperative cognitive dysfunction via the TLR4/NF-κB pathway
Abstract Objectives Clinically, there is no effective therapy for postoperative cognitive dysfunction (POCD). Inflammation after surgery is closely associated with POCD. Methods In this study, we explored the role of sirtuin 1 (SIRT1) in POCD. POCD in mice was induced by cardiac surgery. The mRNA and protein levels of related genes were determined by real-time polymerase chain reaction and western blot, respectively. Plasma concentrations of inflammatory factors were measured using an ELISA kit. Novel object and novel location recognition tests were carried out to measure recognition ability. The Morris water maze (MWM) test was performed to measure learning and memory ability. Results There was a clear decrease in SIRT1 expression after POCD. The SIRT1 activator SRT1720 promoted recognition, learning, and memory ability of mice with POCD. Moreover, SRT1720 treatment greatly inhibited plasma inflammatory cytokine levels and TLR4 and P65 protein expression in the hippocampus of POCD mice. The effect of SRT1720 on POCD was in a TLR4-dependent manner. Conclusions SIRT1 mediates the improvement of cardiac surgery-induced postoperative cognitive dysfunction via the TLR4/NF-κB pathway.
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