Integrating Network Pharmacology and Transcriptomic Strategies to Explore the Pharmacological Mechanism of Paeoniflorin Exerts Antidepressant Effects

IF 1.2 4区 医学 Q4 CHEMISTRY, MEDICINAL
Lili Su, Zixian Wang, Pengli Guo, Zhongmei He, Jianming Li, Yan Zhao, Ying Zong, Weijia Chen, Rui Du
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Abstract

Background:: Paeoniflorin has been proven to have neuroprotective and antidepressant effects in several studies. However, there is currently no comprehensive elaboration of its antidepressant effects through network pharmacology combined with transcriptomics analysis. The purpose of this study is to explore the potential mechanisms by which paeoniflorin exerts its antidepressant effects using network pharmacology and transcriptomics sequencing approaches. Methods:: We utilized metascape to enrich the intersecting targets for paeoniflorin and depression for enrichment analyses. Additionally, we employed Cytoscape software to construct target pathway networks. For the screening of differentially expressed genes (DEGs) altered by paeoniflorin, we sequenced mRNA from the hippocampal tissue of CUMS model mice using the BMKCloud platform. We further enriched their biological functions and signaling pathways by using the Omishare database. The study utilized a combination of network pharmacology and transcriptomics analysis to evaluate the interactions between paeoniflorin and key targets. The results were then verified through a molecular docking process and a subsequent Western blot experiment. Results:: According to a comprehensive analysis, paeoniflorin has 19 key targets that are closely related to its therapeutic effect. Molecular docking revealed that paeoniflorin has a high affinity for HIF-1α, VEGFA, and other targets. Furthermore, protein expression and immunofluorescence staining analysis showed that paeoniflorin significantly increased the expression level of HIF-1α and VEGFA in the hippocampus of depression model mice. Conclusion:: These findings suggest that paeoniflorin may have therapeutic potential in depression through the activation of the HIF-1α-VEGFA pathway.
结合网络药理学和转录组学策略探讨芍药苷抗抑郁作用的药理机制
背景:几项研究已证明芍药苷具有神经保护和抗抑郁作用。然而,目前还没有通过网络药理学结合转录组学分析对其抗抑郁作用进行全面阐述。本研究的目的是利用网络药理学和转录组学测序方法探讨芍药苷发挥抗抑郁作用的潜在机制。方法:利用元景观法对芍药苷和抑药的交叉靶点进行富集分析。此外,我们使用Cytoscape软件构建目标通路网络。为了筛选芍药苷改变的差异表达基因(DEGs),我们使用BMKCloud平台对CUMS模型小鼠海马组织的mRNA进行了测序。我们利用Omishare数据库进一步丰富了它们的生物学功能和信号通路。本研究利用网络药理学和转录组学分析相结合的方法来评估芍药苷与关键靶点之间的相互作用。然后通过分子对接过程和随后的Western blot实验验证结果。结果:综合分析,芍药苷具有19个与其疗效密切相关的关键靶点。分子对接发现芍药苷对HIF-1α、VEGFA等靶点具有高亲和力。此外,蛋白表达和免疫荧光染色分析显示,芍药苷显著提高抑郁模型小鼠海马组织中HIF-1α和VEGFA的表达水平。结论:上述结果提示芍药苷可能通过激活HIF-1α-VEGFA通路对抑郁症有治疗作用。
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来源期刊
CiteScore
1.80
自引率
10.00%
发文量
245
审稿时长
3 months
期刊介绍: Aims & Scope Letters in Drug Design & Discovery publishes letters, mini-reviews, highlights and guest edited thematic issues in all areas of rational drug design and discovery including medicinal chemistry, in-silico drug design, combinatorial chemistry, high-throughput screening, drug targets, and structure-activity relationships. The emphasis is on publishing quality papers very rapidly by taking full advantage of latest Internet technology for both submission and review of manuscripts. The online journal is an essential reading to all pharmaceutical scientists involved in research in drug design and discovery.
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