Possible Involvement of Pirfenidone Metabolites in the Antifibrotic Action of a Therapy for Idiopathic Pulmonary Fibrosis

被引:17
|
作者
Togami, Kohei [1 ,2 ]
Kanehira, Yukimune [2 ]
Tada, Hitoshi [1 ,2 ]
机构
[1] Hokkaido Pharmaceut Univ, Sch Pharm, Div Pharmaceut, Otaru, Hokkaido 0470264, Japan
[2] Ohu Univ, Sch Pharmaceut Sci, Dept Biopharmaceut, Koriyama, Fukushima 9638611, Japan
基金
日本学术振兴会;
关键词
pirfenidone; 5-hydroxypirfenidone; 5-carboxypirfenidone; idiopathic pulmonary fibrosis; lung fibroblast; BLEOMYCIN HAMSTER MODEL; LUNG FIBROSIS; PHARMACOKINETICS; EXPRESSION; LEVEL;
D O I
10.1248/bpb.b13-00452
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pirfenidone (PFD) is the first and only clinically used antifibrotic drug for the treatment of idiopathic pulmonary fibrosis (IPF). This study evaluated the antifibrotic effects of two metabolites of PFD, 5-hydroxypirfenidone (PFD-OH) and 5-carboxypirfenidone (PFD-COOH), on WI-38 cells in an in vitro lung fibroblast model. The inhibitory effects of PFD-OH and PFD-COOH on transforming growth factor-beta 1 (TGF-beta 1)-induced collagen synthesis in WI-38 cells were evaluated by measuring intracellular hydroxyproline, a major component of the protein collagen. PFD-OH and PFD-COOH at 300 and 1000 mu M concentrations significantly decreased the TGF-beta 1-induced hydroxyproline content in WI-38 cells. These results indicate that PFD-OH and PFD-COOH have antifibrotic activities, which inhibit collagen synthesis in fibroblasts. This study suggests that the concentrations of PFD and its metabolites should be considered in clinical therapy for IPF.
引用
收藏
页码:1525 / 1527
页数:3
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