Hossain Rajib, Lee Hyun Jae, Lee Choong Jae
Department of Pharmacology, School of Medicine, Chungnam National University, Daejeon 35015, Republic of Korea.
Brain Korea 21 FOUR Project for Medical Science, Chungnam National University, Daejeon 35015, Republic of Korea.
Biomol Ther (Seoul). 2024 Sep 1;32(5):540-545. doi: 10.4062/biomolther.2024.072. Epub 2024 Aug 2.
In this study, the potential effects of pyronaridine, an antimalarial agent, on airway mucin gene expression were investigated. The human pulmonary epithelial NCI-H292 cells were pretreated with pyronaridine for 30 min and then stimulated with phorbol 12-myristate 13-acetate (PMA) for 24 h. The effect of pyronaridine on the PMA-induced nuclear factor kappa B (NF-κB) signaling pathway was also examined. Pyronaridine inhibited glycoprotein production and mRNA expression of mucins induced by PMA through the inhibition of degradation of inhibitory kappa Bα and NF-κB p65 nuclear translocation. These results suggest that pyronaridine suppresses gene expression of mucin through regulation of the NF-κB signaling pathway in human pulmonary epithelial cells.
在本研究中,考察了抗疟药咯萘啶对气道黏蛋白基因表达的潜在影响。将人肺上皮NCI-H292细胞用咯萘啶预处理30分钟,然后用佛波酯12-肉豆蔻酸酯13-乙酸酯(PMA)刺激24小时。还研究了咯萘啶对PMA诱导的核因子κB(NF-κB)信号通路的影响。咯萘啶通过抑制抑制性κBα的降解和NF-κB p65核转位,抑制PMA诱导的黏蛋白糖蛋白产生和mRNA表达。这些结果表明,咯萘啶通过调节人肺上皮细胞中的NF-κB信号通路来抑制黏蛋白的基因表达。