Kim Mun-Ock, Lee Jae-Won, Lee Jae Kyoung, Song Yu Na, Oh Eun Sol, Ro Hyunju, Yoon Dahye, Jeong Yun-Hwa, Park Ji-Yoon, Hong Sung-Tae, Ryu Hyung Won, Lee Su Ui, Lee Dae Young
Natural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju 28116, Korea.
Rpbio Research Institute, Rpbio Co., Ltd., Suwon 16229, Korea.
Antioxidants (Basel). 2022 Mar 30;11(4):679. doi: 10.3390/antiox11040679.
Cigarette smoke (CS) is a risk factor that can induce airway enlargement, airway obstruction, and airway mucus hypersecretion. Although studies have shown that Korean black ginseng extract (BGE) has potent anti-inflammatory and antioxidant activities, the CS-induced inflammatory responses and molecular mechanisms are yet to be examined. The aim of this study was to examine the effect of BGE on the airway inflammatory response and its molecular mechanisms, using CS/lipopolysaccharides (LPS)-exposed animals and PMA-stimulated human airway epithelial NCI-H292 cells. The results show that BGE inhibited the recruitment of immune cells and the release of inflammatory mediators, such as tumor necrosis factor (TNF)-α and interleukin (IL)-6, monocyte chemoattractant protein (MCP)-1, elastase, and reactive oxygen species (ROS) in the airways of CS/LPS-exposed animals. BGE inhibited mucus secretion and the expression of Mucin 5AC (MUC5AC). Furthermore, BGE exhibited an anti-inflammatory effect by downregulating a signaling pathway mediated by transforming growth factor-β-activated kinase (TAK) 1, an important protein that accelerates inflammation by cigarette smoke (CS). Overall, the findings show that BGE inhibits lung inflammation and mucus secretion by decreasing the activation of TAK1 both in human epithelial cells and in CS/LPS-exposed animals, and could be a potential adjuvant in the treatment and prevention of airway inflammatory diseases caused by airway irritants such as CS.
香烟烟雾(CS)是一种可诱发气道扩张、气道阻塞和气道黏液高分泌的危险因素。尽管研究表明韩国黑参提取物(BGE)具有强大的抗炎和抗氧化活性,但CS诱导的炎症反应及其分子机制尚待研究。本研究的目的是使用暴露于CS/脂多糖(LPS)的动物和经佛波酯(PMA)刺激的人呼吸道上皮NCI-H292细胞,研究BGE对气道炎症反应及其分子机制的影响。结果表明,BGE抑制了免疫细胞的募集以及炎症介质的释放,如肿瘤坏死因子(TNF)-α、白细胞介素(IL)-6、单核细胞趋化蛋白(MCP)-1、弹性蛋白酶和活性氧(ROS)在暴露于CS/LPS的动物气道中的释放。BGE抑制了黏液分泌和黏蛋白5AC(MUC5AC)的表达。此外,BGE通过下调由转化生长因子-β激活激酶(TAK)1介导的信号通路发挥抗炎作用,TAK1是一种因香烟烟雾(CS)而加速炎症的重要蛋白质。总体而言,研究结果表明,BGE通过降低人上皮细胞和暴露于CS/LPS的动物中TAK1的激活来抑制肺部炎症和黏液分泌,并且可能是治疗和预防由CS等气道刺激物引起的气道炎症性疾病的潜在佐剂。