小胶质细胞与NLRP3炎症小体在认知功能障碍中作用的研究进展

Research Progress on the Role of NLRP3 Inflammasome and Microglia in Cognitive Impairment

  • 摘要: 认知功能障碍作为一种常见的神经系统疾病,以认知减退、记忆力和注意力障碍为主要临床表现,严重影响患者的生存质量,是当前医学研究的热点和难点。认知功能障碍的病因及发病机制复杂多样,研究表明慢性持续性神经炎症在其发生发展中发挥关键作用。小胶质细胞、核苷酸结合寡聚化结构域样受体蛋白3(nucleotide-binding oligomerization domain-like receptor protein 3,NLRP3)炎症小体与神经炎症、认知功能障碍密切相关,调控小胶质细胞、NLRP3炎症小体可减少炎症因子、减少β淀粉样蛋白沉积、调控自噬、维持突触稳态,达到减轻神经炎症,进而防治认知功能障碍的作用。因此,阐明小胶质细胞、NLRP3炎症小体及二者共同在认知功能障碍中的作用机制,可为认知功能障碍相关机制的深入研究及临床防治、药物研发提供参考和依据。

     

    Abstract: As a common neurological disease, cognitive impairment is characterized by cognitive decline, memory and attention impairment, which seriously affects the patients' quality of life. The etiology and pathogenesis of cognitive impairment are complex and diverse. Studies have shown that chronic persistent neuroinflammation plays a key role in its development. Microglia and nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3) inflammasome are closely related to neuroinflammation and cognitive impairment. Regulation of microglia and NLRP3 inflammasome can reduce inflammatory factors, reduce amyloid β-protein(Aβ) deposition, regulate autophagy, maintain synaptic homeostasis, thus reducing neuroinflammation and further preventing and treating cognitive impairment. Therefore, exploring the mechanism of microglia and NLRP3 inflammasome as well as their interaction in cognitive impairment can provide some reference and basis for the in-depth study of the mechanism and clinical prevention and treatment of cognitive impairment, and the subsequent development of more efficient drugs.

     

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