Guan Xilong, Zha Linan, Zhu Xiaoling, Rao Xiuqin, Huang Xiangfei, Xiong Yanhong, Guo Youwei, Zhang Mojiao, Zhou Dongshan, Tu Qikun, Wu Jianhang, Wang Xifeng, Hua Fuzhou, Xu Jing
Department of Anesthesiology, Yingtan City People's Hospital, Yingtan, Jiangxi 335099, P.R. China.
Key Laboratory of Anesthesiology of Jiangxi, Nanchang, Jiangxi 330006, P.R. China.
Int J Mol Med. 2025 Oct;56(4). doi: 10.3892/ijmm.2025.5588. Epub 2025 Jul 19.
The complex of proteins S100A8/A9 has been recognized as a major initiator of cognitive disorder onset, including, but not restricted to, neuroinflammation. Cognitive impairment or decline in memory, attention and executive function has been on the rise and is a major public health priority. Several neurological conditions that affect the brain and cognitive processes, including central nervous system diseases such as Alzheimer's disease and stroke, and systemic diseases, such as sepsis and systemic lupus erythematosus, are associated with S100A8/A9. Experiments have progressively demonstrated that S100A8/A9 plays a role in cognitive decline, as it regulates cognitive domains, including sleep, learning, memory, and emotion control, via several mechanisms. In this review, a critical overview of the role of S100A8/A9 in the treatment of neurocognitive diseases is provided, including the regulation of brain function and the pathogenesis of diseases, and potential novel therapies are suggested. It is necessary to study S100A8/A9 alone as an alternative marker for the diagnosis and treatment of neurocognitive diseases, and in line with the requirements of therapy for cognitive impairment. As S100A8/A9 research continues, the understanding and treatment of neurocognitive diseases may improve.
蛋白质S100A8/A9复合物已被公认为认知障碍发病的主要引发因素,包括但不限于神经炎症。认知障碍或记忆力、注意力及执行功能的衰退呈上升趋势,是公共卫生的主要优先事项。几种影响大脑和认知过程的神经系统疾病,包括中枢神经系统疾病如阿尔茨海默病和中风,以及全身性疾病如败血症和系统性红斑狼疮,都与S100A8/A9有关。实验已逐步证明,S100A8/A9在认知衰退中起作用,因为它通过多种机制调节包括睡眠、学习、记忆和情绪控制在内的认知领域。在本综述中,对S100A8/A9在神经认知疾病治疗中的作用进行了批判性概述,包括脑功能调节和疾病发病机制,并提出了潜在的新疗法。有必要单独研究S100A8/A9作为神经认知疾病诊断和治疗的替代标志物,并符合认知障碍治疗的要求。随着对S100A8/A9研究的不断深入,对神经认知疾病的理解和治疗可能会得到改善。