Lu Ruilong, Xu Kexin, Qin Yanqin, Shao Xuejie, Yan Miaomiao, Liao Yixi, Wang Bo, Zhao Jie, Li Jiansheng, Tian Yange
Co-Construction Collaborative Innovation Center for Chinese Medicine and Respiratory Diseases By Henan & Education Ministry of PR, Henan University of Chinese Medicine, Zhengzhou 450046, Henan, China.
Henan Key Laboratory of Chinese Medicine for Respiratory Disease, Henan University of Chinese Medicine, Zhengzhou 450046, Henan, China.
Evid Based Complement Alternat Med. 2022 Nov 3;2022:4838650. doi: 10.1155/2022/4838650. eCollection 2022.
Chronic obstructive pulmonary disease (COPD) is a long-term respiratory disorder marked by restricted airflow and persistent respiratory symptoms. According to previous studies, icariin combined with nobiletin (I&N) significantly ameliorates COPD, but the therapeutic mechanisms remain unclear.
The aim of the study is to investigate the therapeutic mechanisms of I&N against COPD using network pharmacology and experimental validation.
The targets of I&N and related genes of COPD were screened and their intersection was selected. Next, the protein-protein interaction (PPI) networks, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were performed. Further, a COPD rat model was established to validate the effect and mechanisms of I&N.
445 potential targets I&N were obtained from SwissTargetPrediction, STITCH 5.0, and PharmMapper databases. 1831 related genes of COPD were obtained from GeneCards, DrugBank, and DisGeNet databases. 189 related genes were screened via matching COPD targets with I&N. 16 highest score targets among 189 targets were obtained according to PPI networks. GO and KEGG pathway enrichment analyses of 16 highest score targets suggested that these key genes of I&N were mostly enriched in the tumor necrosis factor (TNF) pathway, mitogen-activated protein kinase (MAPK) pathway, and phosphatidyl inositol 3-kinase (PI3K)-protein kinase B (AKT) pathway. Therefore, the treatments of I&N for COPD were connected with inflammation-related pathways. In in vivo experiments, the studies indicated that I&N improved the lung function and alleviated the damage of pulmonary histopathology. Moreover, I&N reduced levels of interleukin (IL)-6, IL-1, and TNF- in lung tissues of COPD rats and inhibited the activation of the MAPK pathway and PI3K-Akt pathway.
Icariin combined with nobiletin has therapeutic effects on COPD by inhibiting inflammation. The potential mechanisms of I&N may relate to the MAPK pathway and PI3K-Akt pathway.
慢性阻塞性肺疾病(COPD)是一种以气流受限和持续呼吸道症状为特征的长期呼吸系统疾病。根据以往研究,淫羊藿苷联合川陈皮素(I&N)可显著改善COPD,但治疗机制尚不清楚。
本研究旨在利用网络药理学和实验验证来探究I&N治疗COPD的机制。
筛选I&N的靶点和COPD的相关基因,并选取它们的交集。接下来,进行蛋白质-蛋白质相互作用(PPI)网络、基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路富集分析。此外,建立COPD大鼠模型以验证I&N的作用效果和机制。
从SwissTargetPrediction、STITCH 5.0和PharmMapper数据库中获得445个I&N潜在靶点。从GeneCards、DrugBank和DisGeNet数据库中获得1831个COPD相关基因。通过将COPD靶点与I&N匹配筛选出189个相关基因。根据PPI网络从189个靶点中获得16个得分最高的靶点。对16个得分最高的靶点进行GO和KEGG通路富集分析表明,I&N的这些关键基因大多富集于肿瘤坏死因子(TNF)通路、丝裂原活化蛋白激酶(MAPK)通路和磷脂酰肌醇3激酶(PI3K)-蛋白激酶B(AKT)通路。因此,I&N对COPD的治疗与炎症相关通路有关。在体内实验中,研究表明I&N改善了肺功能并减轻了肺组织病理学损伤。此外,I&N降低了COPD大鼠肺组织中白细胞介素(IL)-6、IL-1和TNF-的水平,并抑制了MAPK通路和PI3K-Akt通路的激活。
淫羊藿苷联合川陈皮素通过抑制炎症对COPD具有治疗作用。I&N的潜在机制可能与MAPK通路和PI3K-Akt通路有关。