Systematic review of Kaixinsan in treating depression: Efficacy and pharmacological mechanisms

被引:4
|
作者
Bo, Menghan [1 ]
Zhang, Hongjing [2 ]
Xu, Jia [1 ]
Zhao, Hong [2 ]
Jia, Xinglei [1 ]
Wang, Guangdong [3 ]
Lu, Zhengyu [1 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Longhua Hosp, VIP Dept, Shanghai, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Yueyang Hosp Integrated Tradit Chinese & Western M, Teaching Affairs Dept, Shanghai, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Inst Chinese Mat Med, Shanghai, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Kaixinsan; depression; traditional Chinese medicine prescription; network pharmacology; efficacy; KAI-XIN-SAN; MAJOR DEPRESSION; NETWORK PHARMACOLOGY; DISEASE; STRESS; ANTIDEPRESSANTS; PRESCRIPTION; METAANALYSIS; DISORDERS; SYMPTOMS;
D O I
10.3389/fnbeh.2022.1061877
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
IntroductionKaixinsan (KXS) has been in use as an effective classic formulation of traditional Chinese medicine for depression. However, its active components and action mechanism against depression remain elusive. The purpose of this study was to summarize and evaluate the efficacy and potential pharmacological mechanisms of KXS in antidepressant treatment.Materials and methodsReports on the use of KXS in the treatment of depression were systematically collected from PubMed, Web of Science, Embase, China National Knowledge Infrastructure, Chongqing VIP, and Wanfang Data from the establishment to July 2022, including those on mood disorders in neurological diseases such as Alzheimer's disease. Meta-analysis was conducted with the Review Manager 5.3 software. Online datasets, traditional Chinese medicine system pharmacological analysis platform, GeneCards, online Mendelian inheritance in man, and DisGeNET were used to investigate the depression-related genes. The gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichments were performed to construct the 'component-target-pathways' network using Metascape online analyses.ResultTen studies were included in the analysis. Meta-analysis showed that both low-dose KXS (SMD = 19.66, Z = 7.96, and I-2 = 42%) and high-dose KXS (SMD = 23.84, Z = 8.46, and I-2 = 13%) could increase the sucrose preference in depression models. In addition, 5-hydroxytryptamine (5-HT) (SMD = 10.91, Z = 2.95, and I-2 = 50%) returned to normal level after the treatment at low dose KXS. In network pharmacology, 50 active components and 376 gene targets were screened out. AKT1, GAPDH, ALB, TNF, and TP53 were the core target proteins. GO analysis showed that KXS mainly treats depression in biological processes such as response to drugs, cellular calcium ion homeostasis, and regulation of chemical synaptic signal transmission. KEGG results show that the mechanism of action of KXS in treating depression is through neural activity ligand-receptor interaction, the calcium signaling and CAMP signaling pathways.DiscussionThe study reveals the active components and potential molecular mechanism of KXS in the treatment of depression and provides evidence for future basic research.
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页数:15
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