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氯胺酮通过 TLR4/MyD88/p38MAPK 通路改善老年小鼠术后认知功能障碍的作用及机制。

Role and mechanism of esketamine in improving postoperative cognitive dysfunction in aged mice through the TLR4/MyD88/p38 MAPK pathway.

机构信息

Department of Anesthesiology, Qilu Hospital of Shandong University, Jinan, Shandong, China.

Department of Anesthesiology, The 960th Hospital of the PLA Joint Logistics Support Force, Jinan, Shandong, China.

出版信息

Kaohsiung J Med Sci. 2024 Jan;40(1):63-73. doi: 10.1002/kjm2.12778. Epub 2023 Nov 29.

Abstract

Postoperative cognitive dysfunction (POCD) is a significant concern for the elderly population worldwide. This study explored the effects of esketamine on aged mice with POCD and investigate its mechanism of action involving the TLR4/MyD88/MAPK pathway. We administrated esketamine, along with lipopolysaccharide or anisomycin, to the aged POCD mouse models. We assessed their cognitive function using the Morris water maze test. Additionally, we evaluated histopathological changes/neuronal apoptosis in the mouse hippocampal CA1 area through HE/TUNEL stainings. Furthermore, we measured IL-1β/IL-6/TNF-α/TLR4/MyD88/MAPK (p-p38/p38) levels in mouse hippocampal tissues using ELISA/RT-qPCR/Western blotting. Lastly, we analyzed the interaction between TLR4 and MyD88 using a co-immunoprecipitation assay. Our findings showed that esketamine effectively mitigated POCD in aged mice. This was evident from the improved cognitive performance observed in the Morris water maze test, characterized by reduced escape latency/increased number of platform crossing/a higher percentage of time spent in the target quadrant. Furthermore, esketamine exhibited a protective effect against neuronal apoptosis and reduced the levels of inflammatory factors. These findings suggest that esketamine exerts an anti-inflammatory effect by downregulating TLR4/MyD88, thereby attenuating the inflammatory response associated with POCD. Additionally, esketamine suppressed the p38 MAPK pathway by inhibiting the TLR4/MyD88 signaling cascade. Esketamine demonstrated its efficacy in improving postoperative inflammation and cognitive impairment in aged mice by inhibiting the TLR4/MyD88 pathway. The activation of p38 MAPK signaling diminished the beneficial effects of esketamine in aged POCD mice. Collectively, the underlying mechanism of esketamine in mitigating POCD in aged mice involves the suppression of the TLR4/MyD88/p38 MAPK pathway.

摘要

术后认知功能障碍(POCD)是全球老年人群体的一个重要关注点。本研究探讨了氯胺酮对患有 POCD 的老年小鼠的影响,并研究了其涉及 TLR4/MyD88/MAPK 通路的作用机制。我们给老年 POCD 小鼠模型给予氯胺酮,同时给予脂多糖或放线菌酮。我们使用 Morris 水迷宫测试评估它们的认知功能。此外,我们通过 HE/TUNEL 染色评估了小鼠海马 CA1 区的组织病理学变化/神经元凋亡。此外,我们使用 ELISA/RT-qPCR/Western blot 测量了小鼠海马组织中的 IL-1β/IL-6/TNF-α/TLR4/MyD88/MAPK(p-p38/p38)水平。最后,我们使用免疫共沉淀测定分析了 TLR4 和 MyD88 之间的相互作用。我们的研究结果表明,氯胺酮可有效减轻老年小鼠的 POCD。这从 Morris 水迷宫测试中观察到的认知表现改善中得到证实,表现为逃避潜伏期缩短/平台穿越次数增加/目标象限停留时间百分比增加。此外,氯胺酮表现出对神经元凋亡的保护作用,并降低了炎症因子的水平。这些发现表明,氯胺酮通过下调 TLR4/MyD88 发挥抗炎作用,从而减轻与 POCD 相关的炎症反应。此外,氯胺酮通过抑制 TLR4/MyD88 信号级联来抑制 p38 MAPK 通路。氯胺酮通过抑制 TLR4/MyD88 通路,显示出在改善老年小鼠术后炎症和认知障碍方面的功效。p38 MAPK 信号的激活减弱了氯胺酮在老年 POCD 小鼠中的有益作用。综上所述,氯胺酮减轻老年小鼠 POCD 的潜在机制涉及抑制 TLR4/MyD88/p38 MAPK 通路。

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