Department of Anesthesiology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China; Department of Anesthesiology, Cangzhou Central Hospital, Cangzhou, Hebei, China.
Department of Neurosurgery, Cangzhou Central Hospital, Graduate School of Hebei Medical University, Heibei, China.
Brain Res Bull. 2022 Sep;187:169-180. doi: 10.1016/j.brainresbull.2022.07.004. Epub 2022 Jul 14.
Postoperative cognitive decline (POCD) is a common complication after surgery and anesthesia among the elderly. Yet the potential mechanism of POCD remains ambiguous, with limited therapeutic measures currently available. Ketamine has been reported to attenuate POCD after cardiac surgery. Herein, we tried to determine the effect of esketamine (the S-enantiomer of ketamine) on POCD and the possible molecular mechanisms.
We investigated the effects of esketamine (10 mg/kg) on POCD using an exploratory laparotomy model in aged SD rats (24 months). Open field, novel object recognition, and morris water maze tests were performed on day 30 post-surgery. 24 h or 30 d post-surgery, brain tissue from the hippocampus and ventromedial prefrontal cortex (vmPFC) was harvested and subjected to histopathology and molecular biology analysis. During the in vitro experiment, primary astrocytes from the hippocampus and vmPFC were exposed to lipopolysaccharide (LPS) to investigate the pathological changes in astrocytes during the process of POCD.
Our results indicated that exploratory laparotomy could induce significant cognitive and memory decline, accompanied by A2-type astrocytes phenotype loss and increased expression of neuron Aβ-42, astrocytes GABA, stimulator of interferon genes (STING) and TANK-binding kinase 1 (TBK1). In addition, LPS exposure significantly decreased the mitochondrial membrane potential and upregulated the level of pyroptosis-associated proteins, including cleaved caspase-1 and IL-18. Notably, treatment with esketamine reversed these abnormalities in vivo and vitro. However, ADU-S100, a special STING activator, suppressed the protective effects of esketamine to a certain extent. Finally, C-176, an antagonist of STING, further enhanced the protective effects of esketamine against POCD.
Findings of our study suggest that esketamine can alleviate surgery-induced POCD in rats via inhibition of the STING/TBK1 signaling pathway.
术后认知功能障碍(POCD)是老年人手术后和麻醉后的常见并发症。然而,POCD 的潜在机制仍不清楚,目前可用的治疗措施有限。有报道称氯胺酮可减轻心脏手术后的 POCD。在此,我们试图确定 Esketamine(氯胺酮的 S-对映体)对 POCD 的影响及其可能的分子机制。
我们使用老龄 SD 大鼠(24 个月)的剖腹探查模型来研究 Esketamine(10mg/kg)对 POCD 的影响。术后 30 天进行旷场、新物体识别和 Morris 水迷宫测试。术后 24 小时或 30 天,取海马和腹内侧前额叶皮质(vmPFC)的脑组织进行组织病理学和分子生物学分析。在体外实验中,将海马和 vmPFC 的原代星形胶质细胞暴露于脂多糖(LPS)中,以研究星形胶质细胞在 POCD 过程中的病理变化。
我们的结果表明,剖腹探查术可引起明显的认知和记忆下降,伴有 A2 型星形胶质细胞表型丧失和神经元 Aβ-42、星形胶质细胞 GABA、干扰素基因刺激因子(STING)和 TANK 结合激酶 1(TBK1)表达增加。此外,LPS 暴露显著降低了线粒体膜电位,并上调了与细胞焦亡相关的蛋白水平,包括 cleaved caspase-1 和 IL-18。值得注意的是,Esketamine 体内和体外均可逆转这些异常。然而,STING 的特殊激活剂 ADU-S100 在一定程度上抑制了 Esketamine 的保护作用。最后,STING 的拮抗剂 C-176 进一步增强了 Esketamine 对 POCD 的保护作用。
本研究结果表明,Esketamine 通过抑制 STING/TBK1 信号通路可减轻大鼠手术引起的 POCD。