Molecular mechanisms and therapeutic potential of icariin in the treatment of Alzheimer's disease

被引:16
|
作者
Zheng, Lingyan [1 ]
Wu, Sichen [1 ]
Jin, Haichao [1 ]
Wu, Jiaqi [1 ]
Wang, Xiaole [1 ]
Cao, Yuxiao [1 ]
Zhou, Zhihao [2 ]
Jiang, Yaona [3 ]
Li, Linhong [4 ]
Yang, Xinyue [4 ]
Shen, Qing [5 ]
Guo, Shunyuan [6 ]
Shen, Yuejian [7 ]
Li, Changyu [1 ]
Ji, Liting [1 ]
机构
[1] Zhejiang Chinese Med Univ, Sch Pharmaceut Sci, Hangzhou 310006, Peoples R China
[2] Zhejiang Chinese Med Univ, Sch Clin Med 3, Sch Rehabil Med, Hangzhou 310006, Peoples R China
[3] Zhejiang Chinese Med Univ, Clin Med Coll 2, Hangzhou 310006, Peoples R China
[4] Zhejiang Chinese Med Univ, Clin Med Coll 1, Hangzhou 310006, Peoples R China
[5] Zhejiang Gongshang Univ, Inst Seafood, Collaborat Innovat Ctr Seafood Deep Proc, Zhejiang Prov Joint Key Lab Aquat Prod Proc, Hangzhou 310012, Peoples R China
[6] Peoples Hosp Hangzhou Med, Zhejiang Prov Peoples Hosp, Dept Neurol, Hangzhou 310014, Zhejiang, Peoples R China
[7] Hangzhou Linping Hosp Tradit Chinese Med, Linping 311106, Hangzhou, Peoples R China
关键词
Icariin; Alzheimer's disease; Neuronal apoptosis; Neurotransmitter; Anti-inflammatory; SYNAPTIC PLASTICITY; COGNITIVE DEFICITS; MOUSE MODEL; A-BETA; TAU; NEUROTOXICITY; ACTIVATION; MICROGLIA; NEURONS; MEMORY;
D O I
10.1016/j.phymed.2023.154890
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Icariin (ICA) is the main active component of Epimedium, a traditional Chinese medicine (TCM), known to enhance cognitive function in Alzheimer's disease (AD). This study aims to investigate and summarize the mechanisms through which ICA treats AD. Methods: The PubMed and CNKI databases were utilized to review the advancements in ICA's role in AD prevention and treatment by analyzing literature published between January 2005 and April 2023. To further illustrate ICA's impact on AD development, tables, and images are included to summarize the relationships between various mechanisms. Results: The study reveals that ICA ameliorates cognitive deficits in AD model mice by modulating A beta via multiple pathways, including BACE-1, NO/cGMP, Wnt/Ca2+, and PI3K/Akt signaling. ICA exhibits neuroprotective properties by inhibiting neuronal apoptosis through the suppression of ER stress in AD mice, potentially linked to NF-kappa B, MAPK, ERK, and PERK/Eif2 alpha signaling pathways. Moreover, ICA may safeguard neurons by attenuating mitochondrial oxidative stress injury. ICA can also enhance learning, memory, and cognition by improving synaptic structure via regulation of the PSD-95 protein. Furthermore, ICA can mitigate neuroinflammation by inactivating microglial activity through the upregulation of PPAR gamma, TAK1/IKK/NF-kappa B, and JNK/p38 MAPK signaling pathways. Conclusion: This study indicates that ICA possesses multiple beneficial effects in AD treatment. Through the integration of pharmacological and molecular biological research, ICA may emerge as a promising candidate to expedite the advancement of TCM in the clinical management of AD.
引用
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页数:11
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