Korean Red Ginseng water extract inhibits cadmium-induced lung injury via suppressing MAPK/ERK1/2/AP-1 pathway

被引:17
|
作者
Mitra, Ankita [1 ,2 ]
Rahmawati, Laily [1 ,2 ]
Lee, Hwa Pyoung [1 ,2 ]
Kim, Seung A. [1 ,2 ]
Han, Chang-Kyun [3 ]
Hyun, Sun Hee [3 ]
Cho, Jae Youl [1 ,2 ]
机构
[1] Sungkyunkwan Univ, Dept Integrat Biotechnol, Suwon 16419, South Korea
[2] Sungkyunkwan Univ, Biomed Inst Convergence SICKU BICS, Suwon 16419, South Korea
[3] Korea Ginseng Corp, R&D Headquarters, Daejeon, South Korea
基金
新加坡国家研究基金会;
关键词
Korean Red Ginseng; Panax ginseng; Lung injury; Cadmium; Anti-inflammatory activity. AP-1; NF-KAPPA-B; MECHANISM; GINSENOSIDES; ACTIVATION; RESPONSES; KINASE; CELLS;
D O I
10.1016/j.jgr.2022.04.003
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Few studies reported the therapeutic effect of Korean Red Ginseng (KRG) in lung inflammatory diseases. However, the anti-inflammatory role and underlying molecular in cadmium-induced lung injury have been poorly understood, directly linked to chronic lung diseases (CLDs): chronic obstructive pulmonary disease (COPD), cancer etc. Therefore, in this study we aim to investigate the therapeutic activities of water extract of KRG (KRG-WE) in mouse cadmium-induced lung injury model. Method: The anti-inflammatory roles and underlying mechanisms of KRG-WE were evaluated in vitro under cadmium-stimulated lung epithelial cells (A549) and HEK293T cell line and in vivo in cadmiuminduced lung injury mouse model using semi-quantitative polymerase chain reaction (RT-PCR), quantitative real-time PCR (qPCR), luciferase assay, immunoblotting, and FACS. Results: KRG-WE strongly ameliorated the symptoms of CdSO4-induced lung injury in mice according to total cell number in bronchoalveolar lavage fluid (BALE) and severity scores as well as cytokine levels. KRG-WE significantly suppressed the upregulation of inflammatory signaling comprising mitogen-activated protein kinases (MAPK) and their upstream enzymes. In in vitro study, KRG-WE suppressed expression of interleukin (IL)-6, matrix metalloproteinase (MMP)-2, and IL-8 while promoting recovery in CdSO 4 -treated A549 cells. Similarly, KRG-WE reduced phosphorylation of MAPK and c-Jun/c-Fos in cadmium-exposed A549 cells. Conclusion: KRG-WE was found to attenuate symptoms of cadmium-induced lung injury and reduce the expression of inflammatory genes by suppression of MAPK/AP-1-mediated pathway. (C) 2022 The Korean Society of Ginseng. Publishing services by Elsevier B.V.
引用
收藏
页码:690 / 699
页数:10
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