A standardized herbal extract PM014 ameliorates pulmonary fibrosis by suppressing the TGF-β1 pathway

被引:20
作者
Kim, Kyung Hwa [1 ]
Lee, Sujin [1 ]
Lee, Hyunji [1 ]
Shin, Dasom [1 ]
Min, Daeun [1 ]
Kim, Miran [2 ]
Ryu, Byeol [3 ,4 ]
Kim, HyeonWoo [3 ,4 ]
Bae, Hyunsu [1 ]
机构
[1] Kyung Hee Univ, Coll Korean Med, Dept Physiol, Seoul 02447, South Korea
[2] Hanlim Pharm Co Ltd, Cent Res Inst, Yongin 17040, South Korea
[3] Seoul Natl Univ, Coll Pharm, Seoul 08826, South Korea
[4] Seoul Natl Univ, Res Inst Pharmaceut Sci, Seoul 08826, South Korea
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
基金
新加坡国家研究基金会;
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; TGF-BETA; FORMULA PM014; MURINE MODEL; INFLAMMATION; PIRFENIDONE; EXPRESSION; NINTEDANIB; RESPONSES; CAPACITY;
D O I
10.1038/s41598-018-35320-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Idiopathic pulmonary fibrosis (IPF) is a devastating and common chronic lung disease pathologically characterized by loss of epithelial cells and activation of fibroblasts and myofibroblasts. The etiology of IPF remains unclear and the disease pathology is poorly understood with no known efficacious therapy. PM014 is an herbal extract that has been shown to have beneficial effects in pulmonary diseases, which are likely to exert anti-inflammatory bioactions. In the present study, we observed that bleomycin (BLM) caused increased inflammatory infiltration as well as collagen deposition in lungs of mice on day 14 after treatment. Administration of PM014 suppressed BLM-induced inflammatory responses and fibrotic changes in dose-dependent manner in mice. Additionally, we provided in vitro evidence suggesting that PM014 inhibited TGF-beta 1-induced epithelial-mesenchyma I transition (EMT) and fibroblast activation in alveolar epithelial cells and human lung fibroblasts from healthy donor and IPF patients. PM014 appeared to target TGF-beta 1 signaling via Smad-dependent pathways and p38 mitogen-activated protein kinases (MAPKs) pathways. Taken together, our data suggest that PM014 administration exerts a protective effect against lung fibrosis and highlight PM014 as a viable treatment option that may bring benefits to patient with IPF.
引用
收藏
页数:12
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