Liu Xizhen, Zhang Anke
Department of Anesthesiology, The Affiliated People's Hospital of Ningbo University, Ningbo, China.
Department of Neurosurgery, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
CNS Neurosci Ther. 2025 Jul;31(7):e70481. doi: 10.1111/cns.70481.
Perioperative neurocognitive disorders (PND) encompass a spectrum of cognitive impairments that arise from the preoperative phase and can persist for months after surgery, with a prevalence of up to 50% in elderly patients. These disorders, including postoperative delirium and sustained cognitive decline, significantly reduce patient quality of life and impose substantial burdens on healthcare systems. Despite extensive research, the underlying pathophysiological mechanisms remain inadequately understood, limiting the development of effective treatments. Increasing evidence highlights neuroinflammation as a central factor in PND, with microglia-the resident immune cells of the central nervous system-playing a key role in mediating inflammatory responses that lead to cognitive dysfunction.
This review comprehensively analyzes the role of microglia in the pathogenesis of PND. It details key perioperative triggers of microglial activation, such as surgical stress, anesthesia, and systemic inflammation. The review further examines preclinical interventions aimed at modulating microglial function, including depletion strategies, polarization toward anti-inflammatory phenotypes, and inhibition of inflammatory pathways like NF-κB and NLRP3.
Preclinical studies demonstrate that dysregulated microglial activation results in excessive production of pro-inflammatory cytokines, oxidative stress, and synaptic disruptions, which collectively contribute to neuronal injury and cognitive impairment. Interventions targeting microglial activation have shown efficacy in reducing neuroinflammation and preserving cognitive function in animal models.
Targeting microglial activation represents a promising strategy for alleviating PND. However, challenges remain in clinical translation, necessitating advanced drug delivery platforms, personalized therapeutic approaches, and rigorous clinical validation. Advances in microglial modulation hold potential for improving postoperative cognitive outcomes and enhancing patient recovery.
围手术期神经认知障碍(PND)涵盖一系列认知功能损害,这些损害始于术前阶段,术后可持续数月,老年患者中的患病率高达50%。这些障碍,包括术后谵妄和持续性认知功能下降,显著降低患者生活质量,并给医疗系统带来沉重负担。尽管进行了广泛研究,但潜在的病理生理机制仍未得到充分理解,限制了有效治疗方法的开发。越来越多的证据表明神经炎症是PND的核心因素,小胶质细胞——中枢神经系统的常驻免疫细胞——在介导导致认知功能障碍的炎症反应中起关键作用。
本综述全面分析了小胶质细胞在PND发病机制中的作用。详细阐述了小胶质细胞激活的关键围手术期触发因素,如手术应激、麻醉和全身炎症。该综述进一步研究了旨在调节小胶质细胞功能的临床前干预措施,包括清除策略、向抗炎表型极化以及抑制NF-κB和NLRP3等炎症途径。
临床前研究表明,小胶质细胞激活失调会导致促炎细胞因子过度产生、氧化应激和突触破坏,这些共同导致神经元损伤和认知障碍。针对小胶质细胞激活的干预措施已在动物模型中显示出减轻神经炎症和保留认知功能的效果。
针对小胶质细胞激活是减轻PND的一种有前景的策略。然而,临床转化仍面临挑战,需要先进的药物递送平台、个性化治疗方法和严格的临床验证。小胶质细胞调节方面的进展有望改善术后认知结果并促进患者康复。