五藏文阳化瘀汤调节BCL-2/BAX/Caspase3治疗血管性痴呆:综合体外细胞实验和网络药理分析

Yu-Cheng Lu , Yu-Fu Zeng , Yan-Chun Li , Chun-Mei Liang , Ying-Ying Cao , Ling Zhang , Meng-Qi Li , Jia-Jia Zhong , Li-Mei Liang
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引用次数: 0

摘要

目的研究五藏文阳化瘀汤。基于网络药理学和实验验证的血管性痴呆的潜在治疗机制。方法采用stcmsp方法筛选白藜芦醇的有效成分和靶点;GeneCards用于识别dvd相关靶标;使用Cytoscape 3.10.0生成“活性成分-目标”网络图;使用STRING和Cytoscape生成PPI网络图;metscape和WeiShengxin通过GO和KEGG分析筛选潜在的信号通路并探讨其机制;通过细胞实验验证相关靶点。结果共筛选出117个WWHT活性成分,146个基因靶点与VD相交。PPI网络中的高频节点包括CASP3、MMP9、BCL2等。氧化石墨烯分析表明,生物功能涉及激素、氮化合物和其他响应;KEGG分析显示,这些通路主要集中在AGE-RAGE、MAPK等信号通路上。为了治疗VD, WWHT可能会改善缺血-缺氧时HT22的形态,控制凋亡相关蛋白,促进HT22的增殖。结论WWHT是一种多组分、多靶点、多通路的有效治疗VD的手段,具有保护神经元细胞、调节细胞凋亡、减轻脑损伤的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Wuzang Wenyang Huayu Tang Treatment of vascular dementia by modulation of BCL-2/BAX/Caspase3: An integrated in vitro cellular assay and network pharmacological analysis

Wuzang Wenyang Huayu Tang Treatment of vascular dementia by modulation of BCL-2/BAX/Caspase3: An integrated in vitro cellular assay and network pharmacological analysis

Objective

This project explores Wuzang Wenyang Huayu Tang (WWHT) 's potential mechanisms for treating vascular dementia (VD) based on network pharmacology and experimental validation.

Methods

TCMSP was used to screen the active ingredients and targets of WWHT; GeneCards was used to identify VD-related targets; Cytoscape 3.10.0 was used to generate an "active ingredient-target" network map; STRING and Cytoscape were used to generate a PPI network map; Metascape and WeiShengxin performed GO and KEGG analysis to screen potential signaling pathways and explore the mechanisms; cell experiments were performed to verify the relevant targets.

Results

117 active components of WWHT were screened, and 146 gene targets intersected with VD. The high-frequency nodes in the PPI network include CASP3, MMP9, BCL2, etc. GO analysis showed that the biological functions involved hormones, nitrogen compounds, and other responses; KEGG analysis revealed that the pathways were concentrated in the signaling pathways such as AGE-RAGE, MAPK, etc. To treat VD, WWHT may enhance HT22 morphology in ischemia-hypoxia, control apoptosis-related proteins, and promote HT22 proliferation.

Conclusion

As a means to effectively treat VD, WWHT may protect neuronal cells, regulate cell apoptosis, and reduce brain damage by using a multi-component, multi-target, and multi-pathway strategy.
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