Protective Effects of Lithospermum erythrorhizon Against Cerulein-Induced Acute Pancreatitis

作者：Choi Sun Bok; Bae Gi Sang; Jo Il Joo; Seo Seung Hee; Kim Dong Goo; Shin Joon Yeon; Hong Seung Heon; Choi Byung Min; Park Sang Hyun; Song Ho Joon; Park Sung Joo^*

来源：Pancreas, 2015, 44(1): 31-40.

DOI：10.1097/MPA.0000000000000195

• acute pancreatitis
• cytokines
• mitogen-activated protein kinases (MAPKs)
• Lithospermum erythrorhizon
• high-mobility group box protein 1 (HMGB-1)

Objectives We aimed to evaluate the anti-inflammatory and inhibitory effects of Lithospermum erythrorhizon (LE) on cerulein-induced acute pancreatitis (AP) in a mouse model.
Methods Acute pancreatitis was induced via intraperitoneal injection of cerulein (50 g/kg) every hour for 6 times. In the LE, water extract (100, 250, or 500 mg/kg) was administered intraperitoneally 1 hour before the first injection of cerulein. Six hours after AP, blood, the pancreas, and the lung were harvested for further examination. In addition, pancreatic acinar cells were isolated using a collagenase method, and then, we investigated the acinar cell viability and cytokine productions.
Results Treatment with LE reduced pancreatic damage and AP-associated lung injury and attenuated the severity of AP, as evidenced by the reduction in neutrophil infiltration, serum amylase and lipase levels, trypsin activity, and proinflammatory cytokine expression. In addition, treatment with LE inhibited high mobility group box 1 expression in the pancreas during AP. In accordance with in vivo data, LE inhibited the cerulein-induced acinar cell death, cytokine productions, and high-mobility group box 1 expression. Furthermore, LE also inhibited the activation of p38 mitogen-activated protein kinases.
Conclusions These results suggest that LE plays a protective role during the development of AP by inhibiting the activation of p38.

• 出版日期2015-1