Gardenia jasminoides protects against cerulein-induced acute pancreatitis

• Published in: World journal of gastroenterology : WJG 2008-10, Vol.14 (40), p.6188-6194
• Main Authors: Jung, Won-Seok, Chae, Young-Seok, Kim, Do-Yun, Seo, Sang-Wan, Park, Hee-Je, Bae, Gi-Sang, Kim, Tae-Hyeon, Oh, Hyo-Jeong, Yun, Ki-Jung, Park, Rae-Kil, Kim, Jong-Suk, Kim, Eun-Cheol, Hwang, Sung-Yeon, Park, Sung-Joo, Song, Ho-Joon
• Format: Article
• Language: English
• Subjects: Acute Disease; Administration, Oral; Amylases - blood; Animals; Anti-Inflammatory Agents - administration & dosage; Anti-Inflammatory Agents - pharmacology; Basic Research; Body Weight; Ceruletide; Disease Models, Animal; Dose-Response Relationship, Drug; Female; Gardenia; Inflammation Mediators - blood; Interleukin-1beta - blood; Interleukin-6 - blood; Lipase - blood; Lung - drug effects; Lung - immunology; Lung - pathology; Lung Injury - chemically induced; Lung Injury - immunology; Lung Injury - prevention & control; Mice; Mice, Inbred C57BL; Neutrophil Infiltration - drug effects; Organ Size; Pancreas - drug effects; Pancreas - immunology; Pancreas - pathology; Pancreatitis - chemically induced; Pancreatitis - immunology; Pancreatitis - prevention & control; Peroxidase - metabolism; Plant Extracts - pharmacology; RNA, Messenger - metabolism; Tumor Necrosis Factor-alpha - blood
• ISSN: 1007-9327
• DOI: 10.3748/wjg.14.6188

To investigate the effect of Gardenia jasminoides (GJ) on cerulein-induced acute pancreatitis (AP) in mice. C57BL/6 mice weighing 18-20 g were divided into three groups. (1) Normal saline-treated group, (2) treatment with GJ at a dose of 0.1 g/kg, (3) treatment with GJ at a dose of 1 g/kg. GJ was administered orally (n = 6 per group) for 1 wk. Three hours later, the mice were given an intraperitoneal injection of cerulein (50 microg/kg), a stable cholecystokinin (CCK) analogue, every hour for a total of 6 h as described previously. The mice were sacrificed at 6 h after completion of cerulein injections. Blood samples were obtained to determine serum amylase, lipase and cytokine levels. The pancreas was rapidly removed for morphologic examination and scoring. A portion of pancreas was stored at -70 degree and prepared for the measurement of tissue myeloperoxidase (MPO) activity, an indicator of neutrophil sequestration, and for reverse-transcriptase PCR (RT-PCR) and real-time PCR measurements. Treatment with GJ decreased significantly the severity of pancreatitis and pancreatitis-associated lung injury. Treatment with GJ attenuated the severity of AP compared with saline-treated mice, as shown by reduction in pancreatic edema, neutrophil infiltration, serum amylase and lipase levels, serum cytokine levels, and mRNA expression of multiple inflammatory mediators. These results suggest that GJ attenuated the severity of AP as well as pancreatitis-associated lung injury.