Objective: To investigate the effect of modified Xiaochaihu Decoction (小柴胡汤, MXD) on transforming growth factor- [3 1/Sma- and Mad-related proteins (TGF- 13 1/Smads) signaling pathway in rats with chronic pan...Objective: To investigate the effect of modified Xiaochaihu Decoction (小柴胡汤, MXD) on transforming growth factor- [3 1/Sma- and Mad-related proteins (TGF- 13 1/Smads) signaling pathway in rats with chronic pancreatitis (CP) induced by dibutyltin dichloride. Methods: Thirty healthy male Wistar rats were randomly divided into the normal control group, CP group and CP+MXD-treated group. CP was induced by injection of dibutyltin dichloride (DBTC, 7 mg/kg of body weight) into the right caudal vein, and the control rats were treated with vehicle. MXD was given daily by gavage at a dose of 10 g/kg of body weight, starting from the day after CP induction. After 28-day treatment, the n-benzoyl-tyrosyl para-aminobenzoic acid (NBT-PABA) test was carried out to evaluate exocrine pancreatic function. Then, rats were sacrificed, and pancreatic tissues were harvested for histological evaluation. In addition, the mRNA expression of TGF- β 1, TGF- β 1 type Ⅱ receptor (TGF β R 11 ), Smad3 and Smad7 was determined in pancreatic tissues by using real-time polymerase chain reaction. Results: Treatment of CP with MXD improved the PABA recovery, decreased the histological lesion, and reduced the mRNA expression of TGF- β 1, TGF β R 11 and Smad3 (P〈0.05). However, MXD had no effect on Smad7 mRNA level. Conclusions: MXD could protect the pancreas against chronic injury and improve pancreatic exocrine function in DBTC induced rat CP model. Its mechanism may involve inhibition of the TGF-β 1/Smads signaling pathway.展开更多
基金Supported by National Natural Science Foundation of China(No.81102686)
文摘Objective: To investigate the effect of modified Xiaochaihu Decoction (小柴胡汤, MXD) on transforming growth factor- [3 1/Sma- and Mad-related proteins (TGF- 13 1/Smads) signaling pathway in rats with chronic pancreatitis (CP) induced by dibutyltin dichloride. Methods: Thirty healthy male Wistar rats were randomly divided into the normal control group, CP group and CP+MXD-treated group. CP was induced by injection of dibutyltin dichloride (DBTC, 7 mg/kg of body weight) into the right caudal vein, and the control rats were treated with vehicle. MXD was given daily by gavage at a dose of 10 g/kg of body weight, starting from the day after CP induction. After 28-day treatment, the n-benzoyl-tyrosyl para-aminobenzoic acid (NBT-PABA) test was carried out to evaluate exocrine pancreatic function. Then, rats were sacrificed, and pancreatic tissues were harvested for histological evaluation. In addition, the mRNA expression of TGF- β 1, TGF- β 1 type Ⅱ receptor (TGF β R 11 ), Smad3 and Smad7 was determined in pancreatic tissues by using real-time polymerase chain reaction. Results: Treatment of CP with MXD improved the PABA recovery, decreased the histological lesion, and reduced the mRNA expression of TGF- β 1, TGF β R 11 and Smad3 (P〈0.05). However, MXD had no effect on Smad7 mRNA level. Conclusions: MXD could protect the pancreas against chronic injury and improve pancreatic exocrine function in DBTC induced rat CP model. Its mechanism may involve inhibition of the TGF-β 1/Smads signaling pathway.