The effects of glycyrrhizin on acute pancreatitis in mice

This study aimed to investigate the effects of glycyrrhizin on acute pancreatitis in mice. Sixty Balb/c mice were randomly divided into four groups as control group, model group, low dose group and high dose group (n=15). Acute pancreatitis was induced by intraperitoneal injection of Caerulein (100...

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Published inEuropean review for medical and pharmacological sciences Vol. 18; no. 24; p. 3943
Main Author Pan, Y-L
Format Journal Article
LanguageEnglish
Published Italy 01.12.2014
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Abstract This study aimed to investigate the effects of glycyrrhizin on acute pancreatitis in mice. Sixty Balb/c mice were randomly divided into four groups as control group, model group, low dose group and high dose group (n=15). Acute pancreatitis was induced by intraperitoneal injection of Caerulein (100 µg/kg) hourly for 6 times. Mice in low dose group and high dose group received intraperitoneal administration of 15 mg/kg and 45 mg/kg glycyrrhizin respectively 4 hours before Caerulein injection. Mice in four groups were sacrificed in three equal lots at 8, 16 and 24 hours after model construction. High Mobility Group Box-1 (HMGB1) expression and serum levels of amylase, TNF-α and IL-6 were determined. The pancreatic tissues were taken for histopathologic analysis. Amylase, TNF-α, IL-6 and HMGB1 levels were significantly higher and pancreas lesion was severer in model group than in control group. However, Amylase, TNF-α, IL-6 and HMGB1 levels in low dose group and high dose group decreased significantly compared with model group. The pancreas lesion was also improved after administration of glycyrrhizin. Glycyrrhizin could decrease the levels of pro-inflammatory cytokines and downregulate the expression of HMGB1 which finally improved the pancreas lesion in mice with acute pancreatitis.
AbstractList This study aimed to investigate the effects of glycyrrhizin on acute pancreatitis in mice. Sixty Balb/c mice were randomly divided into four groups as control group, model group, low dose group and high dose group (n=15). Acute pancreatitis was induced by intraperitoneal injection of Caerulein (100 µg/kg) hourly for 6 times. Mice in low dose group and high dose group received intraperitoneal administration of 15 mg/kg and 45 mg/kg glycyrrhizin respectively 4 hours before Caerulein injection. Mice in four groups were sacrificed in three equal lots at 8, 16 and 24 hours after model construction. High Mobility Group Box-1 (HMGB1) expression and serum levels of amylase, TNF-α and IL-6 were determined. The pancreatic tissues were taken for histopathologic analysis. Amylase, TNF-α, IL-6 and HMGB1 levels were significantly higher and pancreas lesion was severer in model group than in control group. However, Amylase, TNF-α, IL-6 and HMGB1 levels in low dose group and high dose group decreased significantly compared with model group. The pancreas lesion was also improved after administration of glycyrrhizin. Glycyrrhizin could decrease the levels of pro-inflammatory cytokines and downregulate the expression of HMGB1 which finally improved the pancreas lesion in mice with acute pancreatitis.
Author Pan, Y-L
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  fullname: Pan, Y-L
  email: yonglipan@yeah.net
  organization: Department of Emergency Medicine, People's Hospital of Zhengzhou, Zhengzhou, Henan Province, China. yonglipan@yeah.net
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25555888$$D View this record in MEDLINE/PubMed
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Snippet This study aimed to investigate the effects of glycyrrhizin on acute pancreatitis in mice. Sixty Balb/c mice were randomly divided into four groups as control...
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StartPage 3943
SubjectTerms Acute Disease
Amylases - blood
Animals
Dose-Response Relationship, Drug
Down-Regulation - drug effects
Glycyrrhizic Acid - pharmacology
HMGB1 Protein - biosynthesis
Interleukin-6 - blood
Mice
Mice, Inbred BALB C
Pancreatitis - blood
Pancreatitis - drug therapy
Pancreatitis - metabolism
Pancreatitis - pathology
Random Allocation
Tumor Necrosis Factor-alpha - blood
Title The effects of glycyrrhizin on acute pancreatitis in mice
URI https://www.ncbi.nlm.nih.gov/pubmed/25555888
Volume 18
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