Jianpiyifei II Granules Suppress Apoptosis of Bronchial Epithelial Cells in Chronic Obstructive Pulmonary Disease via Inhibition of the Reactive Oxygen Species-Endoplasmic Reticulum Stress-Ca2+ Signaling Pathway

被引:15
|
作者
Fan, Long [1 ]
Li, Leng [1 ]
Yu, Xuhua [1 ]
Liang, Ziyao [1 ]
Cai, Tiantian [1 ]
Chen, Yuanbin [1 ]
Xu, Yinji [1 ]
Hu, Tao [1 ]
Wu, Lei [1 ]
Lin, Lin [1 ]
机构
[1] Guangzhou Univ Chinese Med, Guangdong Prov Key Lab Res Emergency TCM, Clin Coll 2, Guangzhou, Peoples R China
来源
FRONTIERS IN PHARMACOLOGY | 2020年 / 11卷
基金
中国国家自然科学基金;
关键词
chronic obstructive pulmonary disease; Jianpiyifei II; endoplasmic reticulum stress; bronchial epithelial cell; apoptosis; UNFOLDED PROTEIN RESPONSE; ENDOTHELIAL GROWTH-FACTOR; CIGARETTE-SMOKE; ASTRAGALOSIDE IV; LUNG; DEATH; MECHANISMS; CALCIUM; DYSFUNCTION; PREVENTION;
D O I
10.3389/fphar.2020.00581
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Jianpiyifei II granules (JPYF II), a herbal formula, are used for the treatment of chronic obstructive pulmonary disease (COPD) in Guangdong Provincial Hospital of Chinese Medicine. The protective effects of JPYF II against bronchial epithelial cell apoptosis in mice exposed to cigarette smoke (CS) and apoptosis of human bronchial epithelial cell lines (BEAS-2B and 16-HBE) stimulated with cigarette smoke extract (CSE) were investigated. Mice were exposed to CS generated from four cigarettes/day for 30 days and administered a dose of JPYF II (0.75, 1.5, and 3 g/kg/d) from the 3rd week of CS exposure. In mice exposed to CS, JPYF II significantly inhibited CS-induced apoptosis and overexpression of endoplasmic reticulum (ER) stress-related markers in bronchial epithelial cells of the lung tissues. In CSE-stimulated BEAS-2B and 16-HBE cells, JPYF II attenuated apoptosis and cell cycle arrest in the G(0)/G(1) phase. Mechanistically, CSE initially induced intracellular reactive oxygen species (ROS) production, which then triggered ER stress, leading to the release of Ca2+ from ER inositol trisphosphate receptor (IP3R)-mediated stores and finally cell death. Treatment with JPYF II resulted in a significant reduction in CSE-induced apoptosis through interruption of the ROS-ER stress-Ca2+ signaling pathway. Therefore, the results of this study have revealed the underlying mechanism of action of JPYF II in the treatment of COPD.
引用
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页数:15
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