天然产物研究与开发 ›› 2026, Vol. 38 ›› Issue (5): 1058-1065.doi: 10.16333/j.1001-6880.2026.5.014 cstr: 32307.14.1001-6880.2026.5.014

• 开发研究 • 上一篇    下一篇

基于p38 MAPK/NF-κB信号通路探讨裸花紫珠抗呼吸道合胞病毒的作用机制

邵冰梅1,2,崔俊丽1,2,田景振3,侯  林1,2*   

  1. 1山东中医药大学海洋中药研究院;2山东中医药大学青岛中医药科学院,青岛 266000;3山东协和学院,济南 250109
  • 出版日期:2026-05-26 发布日期:2026-05-26
  • 基金资助:
    山东省重点研发计划(重大科技创新工程)(2021CXGC010511);山东省自然科学基金(ZR2019QH007);国家中医药管理局高水平中医药重点学科-中药药剂学(国中医药人教函[2023]85号)

Anti-respiratory syncytial virus mechanism of Callicarpae Nudiflorae Folium based on the p38 MAPK/NF-κB signaling pathway

SHAO Bing-mei1,2,CUI Jun-li1,2,TIAN Jing-zhen3,HOU Lin 1,2*   

  1. 1Marine Chinese Medicine Research Institute of Shandong University of Traditional Chinese Medicine;2Qingdao Academy of Chinese Medicinal Sciences,Shandong University of Traditional Chinese Medicine,Qingdao 266000,China;3Shandong Xiehe University,Jinan 250109,China
  • Online:2026-05-26 Published:2026-05-26

摘要:

基于p38丝裂原活化蛋白激酶/核因子κB(p38 mitogen-activated protein kinase/nuclear factor kappa B,p38 MAPK/NF-κB)信号通路探讨裸花紫珠(Callicarpae Nudiflorae Folium,CNF)提取物抗呼吸道合胞病毒(respiratory syncytial virus,RSV)的作用机制。体外采用细胞病变效应法,以选择指数(selectivity index,SI)为指标考察CNF抗RSV作用;体内建立了小鼠RSV感染模型,以小鼠肺指数、肺病毒载量、肺组织病理变化情况、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)、白细胞介素-1β(interleukin-1β,IL-1β)细胞因子的分泌水平研究CNF的体内抗RSV作用,RT-qPCR法检测p38 MAPK/NF-κB信号通路相关基因mRNA表达,Western blot法检测p38 MAPK/NF-κB信号通路相关蛋白表达。实验结果表明,体外研究表明CNF具有抗RSV作用,SI值为12.10,IC50为26.10 µg/mL;体内研究表明RSV感染小鼠肺指数的升高,与模型组比较,CNF给药组小鼠肺指数、肺病毒载量显著下降,肺组织的肺泡壁增厚程度、淋巴细胞和中性粒细胞的浸润程度明显地降低,同时,CNF给药组小鼠TNF-α、IL-1β炎性细胞因子的分泌水平显著低于模型组,可以显著降低p38 MAPK、p65 NF-κB、核因子κB抑制蛋白α(inhibitor of nuclear factor kappa B alpha,IκBα的mRNA和蛋白的表达。本研究表明CNF具有抗RSV作用,其作用机制可能与p38 MAPK/NF-κB通路发挥免疫调节和抗炎作用相关。

关键词: 裸花紫珠, 呼吸道合胞病毒, p38 MAPK/NF-κB信号通路

Abstract:

This study investigated the anti-respiratory syncytial virus (RSV) mechanism of Callicarpae Nudiflorae Folium(CNF) extract based on the p38 mitogen-activated protein kinase/nuclear factor kappa B (p38 MAPK/NF-κB) signaling pathway. In vitro, the cytopathic effect assay was employed to evaluate the anti-RSV activity of CNF, with the selectivity index (SI) as the primary indicator. In vivo, an RSV-infected mouse model was established to assess the anti-RSV effects of CNF by monitoring lung index, lung viral load, histopathological changes in lung tissue, and secretion levels of inflammatory cytokines, including tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β). The mRNA expression of genes associated with the p38 MAPK/NF-κB pathway was analyzed using RT-qPCR, and protein expression was detected via Western blot. In vitro studies demonstrated that CNF possesses anti-RSV activity, with SI of 12.10 and IC50 of 26.10 µg/mL. In vivo results showed that RSV infection significantly increased the lung index in mice. Compared to the model group, the CNF group exhibited a notable reduction in lung index and lung viral load, along with alleviated histopathological changes in lung tissue, including decreased alveolar wall thickening and reduced infiltration of lymphocytes and neutrophils. Furthermore, CNF group significantly lowered the secretion levels of pro-inflammatory cytokines TNF-α and IL-1β and downregulated the mRNA and protein expression of p38 MAPK, p65 NF-κB, and inhibitor of nuclear factor kappa B alpha (IκBα). These findings suggest that CNF exerts anti-RSV effects, likely through immunomodulatory and anti-inflammatory mechanisms mediated by the p38 MAPK/NF-κB signaling pathway.

Key words: Callicarpae Nudiflorae Folium, anti-respiratory syncytial virus, p38 MAPK/NF-κB signaling pathway

中图分类号:  R285