School of Basic Medical Science, Yunnan University of Chinese Medicine, Kunming, P. R. China.
Heze Hospital of Traditional Chinese Medicine, Heze, P. R. China.
COPD. 2024 Dec;21(1):2329282. doi: 10.1080/15412555.2024.2329282. Epub 2024 Apr 15.
COPD is an inflammatory lung disease that limits airflow and remodels the pulmonary vascular system. This study delves into the therapeutic potential and mechanistic underpinnings of Saponins (PNS) in alleviating inflammation and pulmonary vascular remodeling in a COPD rat model. Symmap and ETCM databases provided -related target genes, and the CTD and DisGeNET databases provided COPD-related genes. Intersection genes were subjected to protein-protein interaction analysis and pathway enrichment to identify downstream pathways. A COPD rat model was established, with groups receiving varying doses of PNS and a Roxithromycin control. The pathological changes in lung tissue and vasculature were examined using histological staining, while molecular alterations were explored through ELISA, RT-PCR, and Western blot. Network pharmacology research suggested PNS may affect the TLR4/NF-κB pathway linked to COPD development. The study revealed that, in contrast to the control group, the COPD model exhibited a significant increase in inflammatory markers and pathway components such as TLR4, NF-κB, HIF-1α, VEGF, ICAM-1, SELE mRNA, and serum TNF-α, IL-8, and IL-1β. Treatment with PNS notably decreased these markers and mitigated inflammation around the bronchi and vessels. Taken together, the study underscores the potential of PNS in reducing lung inflammation and vascular remodeling in COPD rats, primarily modulation of the TLR4/NF-κB/HIF-1α/VEGF pathway. This research offers valuable insights for developing new therapeutic strategies for managing and preventing COPD.
COPD 是一种炎症性肺部疾病,会限制气流并重塑肺部血管系统。本研究深入探讨了皂苷(PNS)在缓解 COPD 大鼠模型中炎症和肺血管重塑方面的治疗潜力和机制基础。Symmap 和 ETCM 数据库提供了相关的靶基因,CTD 和 DisGeNET 数据库提供了 COPD 相关的基因。对交集基因进行了蛋白质-蛋白质相互作用分析和通路富集,以确定下游通路。建立了 COPD 大鼠模型,各组接受不同剂量的 PNS 和罗红霉素对照治疗。通过组织学染色检查肺组织和血管的病理变化,通过 ELISA、RT-PCR 和 Western blot 探索分子变化。网络药理学研究表明,PNS 可能影响与 COPD 发展相关的 TLR4/NF-κB 通路。研究表明,与对照组相比,COPD 模型的炎症标志物和通路成分(如 TLR4、NF-κB、HIF-1α、VEGF、ICAM-1、SELE mRNA 和血清 TNF-α、IL-8 和 IL-1β)显著增加。PNS 治疗显著降低了这些标志物,并减轻了支气管和血管周围的炎症。综上所述,该研究强调了 PNS 减少 COPD 大鼠肺部炎症和血管重塑的潜力,主要是通过 TLR4/NF-κB/HIF-1α/VEGF 通路的调节。这项研究为开发管理和预防 COPD 的新治疗策略提供了有价值的见解。