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CDB石油醚部位的抗抑郁作用及潜在机制:基于网络药理学与代谢组学的整合研究

The anti-depression effect and potential mechanism of the petroleum ether fraction of CDB: Integrated network pharmacology and metabolomics.

作者信息

Zeng Jiuseng, Chen Li, Peng Xi, Luan Fei, Hu Jingwen, Xie Zhiqiang, Xie Hongxiao, Liu Rong, Lv Haizhen, Zeng Nan

机构信息

State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, 611137, China.

Department of Pharmacy, Clinical Medical College and the First Affiliated Hospital of Chengdu Medical College, Chengdu, 610500, China.

出版信息

Heliyon. 2024 Mar 27;10(7):e28582. doi: 10.1016/j.heliyon.2024.e28582. eCollection 2024 Apr 15.

Abstract

The combination of Chaidangbo (CDB) is an antidepressant traditional Chinese medicine (TCM) prescription simplified by Xiaoyaosan (a classic antidepressant TCM prescription) through dismantling research, which has the effect of dispersing stagnated liver qi and nourishing blood in TCM theory. Although the antidepressant effect of CBD has been confirmed in animal studies, the material basis and possible molecular mechanism for antidepressant activity in CBD have not been clearly elucidated. Herein, we investigated the effects and potential mechanisms of CDB antidepressant fraction (petroleum ether fraction of CDB, PEFC) on chronic unpredictable mild stress (CUMS)-induced depression-like behavior in mice using network pharmacology and metabolomics. First, a UPLC-QE/MS was employed to identify the components of PEFC. To extract active ingredients, SwissADME screening was used to the real PEFC components that were found. Potential PEFC antidepressant targets were predicted based on a network pharmacology approach, and a pathway enrichment analysis was performed for the predicted targets. Afterward, a CUMS mouse depression model was established and LC-MS-based untargeted hippocampal metabolomics was performed to identify differential metabolites, and related metabolic pathways. Finally, the protein expressions in mouse hippocampi were determined by Western blot to validate the network pharmacology and metabolomics deduction. A total of 16 active compounds were screened in SwissADME that acted on 73 core targets of depression, including STAT3, MAPKs, and NR3C1; KEGG enrichment analysis showed that PEFC modulated signaling pathways such as PI3K-Akt signaling pathway, endocrine resistance, and MAPK to exert antidepressant effects. PEFC significantly reversed abnormalities of hippocampus metabolites in CUMS mice, mainly affecting the synthesis and metabolism of glycine, serine, and threonine, impacting catecholamine transfer and cholinergic synapses and regulating the activity of the mTOR signaling pathway. Furthermore, Western blot analysis confirmed that PEFC significantly influenced the main protein levels of the PI3K/Akt/mTOR signaling pathways in the hippocampus of mice subjected to CUMS. This study integrated metabolomics, network pharmacology and biological verification to explore the potential mechanism of PEFC in treating depression, which is related to the regulation of amino acid metabolism dysfunction and the activation of PI3K/Akt/mTOR signaling pathways in the hippocampus. The comprehensive strategy also provided a reasonable way for unveiling the pharmacodynamic mechanisms of multi-components, multi-targets, and multi-pathways in TCM with antidepressant effect.

摘要

柴丹波(CDB)合剂是通过拆方研究从小柴胡散(经典抗抑郁中药方剂)简化而来的抗抑郁中药方剂,在中医理论中具有疏肝理气、养血的功效。虽然CDB的抗抑郁作用已在动物研究中得到证实,但其抗抑郁活性的物质基础和可能的分子机制尚未明确阐明。在此,我们运用网络药理学和代谢组学研究了CDB抗抑郁组分(CDB的石油醚组分,PEFC)对慢性不可预测轻度应激(CUMS)诱导的小鼠抑郁样行为的影响及潜在机制。首先,采用超高效液相色谱-四极杆飞行时间质谱联用仪(UPLC-QE/MS)鉴定PEFC的成分。为提取活性成分,利用SwissADME筛选法筛选出实际存在的PEFC成分。基于网络药理学方法预测潜在的PEFC抗抑郁靶点,并对预测靶点进行通路富集分析。随后,建立CUMS小鼠抑郁模型,进行基于液相色谱-质谱联用(LC-MS)的非靶向海马代谢组学分析,以鉴定差异代谢物及相关代谢通路。最后,通过蛋白质免疫印迹法检测小鼠海马中的蛋白表达,以验证网络药理学和代谢组学的推断。在SwissADME中共筛选出16种活性化合物,它们作用于73个抑郁症核心靶点,包括信号转导和转录激活因子3(STAT3)、丝裂原活化蛋白激酶(MAPKs)和核受体亚家族3成员C1(NR3C1);京都基因与基因组百科全书(KEGG)富集分析表明,PEFC通过调节磷脂酰肌醇-3激酶-蛋白激酶B(PI3K-Akt)信号通路、内分泌抵抗和丝裂原活化蛋白激酶(MAPK)等信号通路发挥抗抑郁作用。PEFC显著逆转了CUMS小鼠海马代谢物的异常,主要影响甘氨酸、丝氨酸和苏氨酸的合成与代谢,影响儿茶酚胺转运和胆碱能突触,并调节哺乳动物雷帕霉素靶蛋白(mTOR)信号通路的活性。此外,蛋白质免疫印迹分析证实,PEFC显著影响了CUMS小鼠海马中PI3K/Akt/mTOR信号通路的主要蛋白水平。本研究整合代谢组学、网络药理学和生物学验证,探讨了PEFC治疗抑郁症的潜在机制,这与调节氨基酸代谢功能障碍和激活海马中的PI3K/Akt/mTOR信号通路有关。该综合策略也为揭示具有抗抑郁作用的中药多成分、多靶点、多通路的药效机制提供了合理途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4be6/10998071/1022f687ad66/gr1.jpg

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