Preventive Effects of Gardenia jasminoides on Cerulein-Induced Chronic Pancreatitis

Author:

Choi Ji-Won12,Jeong Jun-Hyeok1,Jo Il-Joo3,Kim Dong-Gu2,Shin Joon Yeon1,Kim Myoung-Jin1,Choi Byung-Min4,Shin Yong Kook5,Song Ho-Joon1,Bae Gi-Sang62,Park Sung-Joo12

Affiliation:

1. Department of Herbology, Wonkwang University School of Korean Medicine, Iksan 54538, Republic of Korea

2. Hanbang Cardio-Renal Syndrome Research Center, Wonkwang University, Iksan 54538, Republic of Korea

3. Division of Beauty Sciences, Wonkwang University School of Natural Sciences, Iksan 54538, Republic of Korea

4. Department of Biochemistry, Wonkwang University School of Medicine, Iksan 54538, Republic of Korea

5. Major in Integrated Oriental Medical Bioscience, College of Health Biotechnology, Semyung University, Jecheon 27136, Republic of Korea

6. Department of Pharmacology, Wonkwang University School of Korean Medicine, Iksan 54538, Republic of Korea

Abstract

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[Formula: see text]g/kg) or saline (control group) were intraperitoneally injected 1[Formula: see text]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 signal-regulated 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.

Funder

National Research Foundation of Korea

Publisher

World Scientific Pub Co Pte Lt

Subject

Complementary and alternative medicine,General Medicine

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