Preventive Effects of Gardenia jasminoides on Cerulein-Induced Chronic Pancreatitis

被引:6
作者
Choi, Ji-Won [1 ,3 ]
Jeong, Jun-Hyeok [1 ]
Jo, Il-Joo [4 ]
Kim, Dong-Gu [3 ]
Shin, Joon Yeon [1 ]
Kim, Myoung-Jin [1 ]
Choi, Byung-Min [5 ]
Shin, Yong Kook [6 ]
Song, Ho-Joon [1 ]
Bae, Gi-Sang [2 ,3 ]
Park, Sung-Joo [1 ,3 ]
机构
[1] Wonkwang Univ, Sch Korean Med, Dept Herbol, 460 Iksandaero, Iksan 54538, Jeonbuk, South Korea
[2] Wonkwang Univ, Sch Korean Med, Dept Pharmacol, 460 Iksandaero, Iksan 54538, Jeonbuk, South Korea
[3] Wonkwang Univ, Hanbang Cardiorenal Syndrome Res Ctr, Iksan 54538, South Korea
[4] Wonkwang Univ, Sch Nat Sci, Div Beauty Sci, Iksan 54538, South Korea
[5] Wonkwang Univ, Sch Med, Dept Biochem, Iksan 54538, South Korea
[6] Semyung Univ, Coll Hlth Biotechnol, Major Integrated Oriental Med Biosci, Jecheon 27136, South Korea
来源
AMERICAN JOURNAL OF CHINESE MEDICINE | 2020年 / 48卷 / 04期
基金
新加坡国家研究基金会;
关键词
Chronic Pancreatitis; Fibrosis; Gardenia jasminoides; Pancreatic Stellate Cells; STELLATE CELLS; HEREDITARY PANCREATITIS; INSIGHTS; FIBROGENESIS; FIBROSIS; DISEASES; ALCOHOL; MODEL; FRUIT;
D O I
10.1142/S0192415X20500470
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Our previous report revealed that Gardenia jasminoides (GJ) has protective effects against acute pancreatitis. So, we examined whether aqueous extract of GJ has anti-inflammation and antifibrotic effects even against cerulein-induced chronic pancreatitis (CP). CP was induced in mice by an intraperitoneal injection of a stable cholecystokinin (CCK) analogue, cerulein, six times a day, four days per week for three weeks. GJ extract (0.1 or 1 g/kg) or saline (control group) were intraperitoneally injected 1 h before first cerulein injection. After three weeks of stimulation, the pancreas was harvested for the examination of several fibrotic parameters. In addition, pancreatic stellate cells (PSCs) were isolated using gradient methods to examine the antifibrogenic effects of GJ. In the cerulein-induced CP mice, the histological features of the pancreas showed severe tissue damage such as enlarged interstitial spaces, inflammatory cell infiltrate and glandular atrophy, and tissue fibrosis. However, treatment of GJ reduced the severity of CP such as pancreatic edema and inflammatory cell infiltration. Furthermore, treatment of GJ increased pancreatic acinar cell survival, and reduced pancreatic fibrosis and activation of PSC in vivo and in vitro. In addition, GJ treatment inhibited the activation of c-Jun N-terminal kinase (JNK) and extracellular signalregulated protein kinase (ERK) in the PSCs. These results suggest that GJ attenuated the severity of CP and the pancreatic fibrosis by inhibiting JNK and ERK activation during CP.
引用
收藏
页码:987 / 1003
页数:17
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