Stem bark of Fraxinus rhynchophylla ameliorates the severity of pancreatic fibrosis by regulating the TGF-β/Smad signaling pathway

被引:3
作者
Choi, Ji-Won [1 ,2 ]
Shin, Joon Yeon [1 ]
Zhou, Ziqi [1 ]
Kim, Dong-Uk [2 ]
Kweon, Bitna [1 ]
Oh, Hyuncheol [3 ]
Kim, Youn-Chul [3 ]
Song, Ho-Joon [1 ]
Bae, Gi-Sang [2 ,4 ,5 ]
Park, Sung-Joo [1 ,2 ]
机构
[1] Wonkwang Univ, Sch Korean Med, Dept Herbol, Iksan, Jeollabuk Do, South Korea
[2] Wonkwang Univ, Hanbang Cardiorenal Syndrome Res Ctr, Sch Korean Med, Iksan, Jeollabuk Do, South Korea
[3] WonkwangUniv, Coll Pharm, Inst Pharmaceut Res & Dev, Iksan, Jeollabuk Do, South Korea
[4] Wonkwang Univ, Sch Korean Med, Dept Pharmacol, Iksan, Jeollabuk Do, South Korea
[5] Wonkwang Univ, Res Ctr Tradit Korean Med, Iksan, Jeollabuk Do, South Korea
基金
新加坡国家研究基金会;
关键词
pancreatitis; fibroblasts; transforming growth factors; GROWTH-FACTOR-BETA; STELLATE CELL ACTIVATION; HEREDITARY PANCREATITIS; EXTRACELLULAR-MATRIX; CANCER; INFLAMMATION; INHIBITION; INSIGHTS; ROLES;
D O I
10.1136/jim-2021-002169
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic pancreatitis (CP) is a pathological fibroinflammatory syndrome of the pancreas. Currently, there are no therapeutic agents available for treating CP-associated pancreatic fibrosis. Fraxinus rhynchophylla (FR) reportedly exhibits anti-inflammatory, antioxidative and antitumor activities. Although FR possesses numerous properties associated with the regulation of diverse diseases, the effects of FR on CP remain unknown. Herein, we examined the effects of FR on CP. For CP induction, mice were intraperitoneally administered cerulein (50 mu g/kg) 6 times a day, 4 days per week for 3 weeks. FR extract (100 or 400 mg/kg) or saline (control group) was intraperitoneally injected 1 hour before the first cerulein injection. After 3 weeks, the pancreas was harvested for histological analysis. In addition, pancreatic stellate cells (PSCs) were isolated to examine the antifibrogenic effects and regulatory mechanisms of FR. Administration of FR significantly inhibited histological damage in the pancreas, increased pancreatic acinar cell survival, decreased PSC activation and collagen deposition, and decreased pro-inflammatory cytokines. Moreover, FR treatment inhibited the expression of fibrotic mediators, such as alpha-smooth muscle actin (alpha-SMA), collagen, fibronectin 1, and decreased pro-inflammatory cytokines in isolated PSCs stimulated with transforming growth factor (TGF)-beta. Furthermore, FR treatment suppressed the phosphorylation of Smad 2/3 but not of Smad 1/5 in TGF-beta-stimulated PSCs. Collectively, these results suggest that FR ameliorates pancreatic fibrosis by inhibiting PSC activation during CP.
引用
收藏
页码:1285 / 1292
页数:8
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