A Japanese herbal medicine (kampo), hochuekkito (TJ-41), has anti-inflammatory effects on the chronic obstructive pulmonary disease mouse model

被引:0
作者
Yuki, Masaaki [1 ]
Ishimori, Taro [1 ]
Kono, Shiho [1 ]
Nagoshi, Saki [1 ]
Saito, Minako [1 ]
Isago, Hideaki [1 ,2 ]
Tamiya, Hiroyuki [1 ,3 ]
Fukuda, Kensuke [1 ]
Miyashita, Naoya [1 ]
Ishii, Takashi [1 ,3 ]
Matsuzaki, Hirotaka [1 ,4 ]
Hiraishi, Yoshihisa [1 ]
Saito, Akira [1 ]
Jo, Taisuke [1 ,5 ]
Nagase, Takahide [1 ]
Mitani, Akihisa [1 ]
机构
[1] Univ Tokyo, Dept Resp Med, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1138655, Japan
[2] Univ Tokyo Hosp, Grad Sch Med, Dept Clin Lab Med, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1138655, Japan
[3] Univ Tokyo, Div Hlth Serv Promot, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1130033, Japan
[4] Univ Tokyo Hosp, Ctr Epidemiol & Prevent Med, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1138655, Japan
[5] Univ Tokyo, Dept Hlth Serv Res, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1138655, Japan
关键词
IMPROVES SYSTEMIC INFLAMMATION; ELDERLY-PATIENTS; LIPOPOLYSACCHARIDE; EXPRESSION; EMPHYSEMA; CELLS;
D O I
10.1038/s41598-024-60646-x
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
Chronic obstructive pulmonary disease (COPD) is a progressive disease that is characterized by chronic airway inflammation. A Japanese herbal medicine, hochuekkito (TJ-41), is prominently used for chronic inflammatory diseases in Japan. This study aimed to analyze the anti-inflammatory effect of TJ-41 in vivo and its underlying mechanisms. We created a COPD mouse model using intratracheal administration of porcine pancreatic elastase and lipopolysaccharide (LPS) and analyzed them with and without TJ-41 administration. A TJ-41-containing diet reduced inflammatory cell infiltration of the lungs in the acute and chronic phases and body weight loss in the acute phase. In vitro experiments revealed that TJ-41 treatment suppressed the LPS-induced inflammatory cytokines in BEAS-2B cells. Furthermore, TJ-41 administration activated the AMP-activated protein kinase (AMPK) pathway and inhibited the mechanistic target of the rapamycin (mTOR) pathway, both in cellular and mouse experiments. We concluded that TJ-41 administration reduced airway inflammation in the COPD mouse model, which might be regulated by the activated AMPK pathway, and inhibited the mTOR pathway.
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页数:13
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