Modified Xiaochaihu Decoction ((sic)&x5473;(sic)&x67f4;&x80e1;&x6c64;) Promotes Collagen Degradation and Inhibits Pancreatic Fibrosis in Chronic Pancreatitis Rats

被引:15
作者
Zhang, Shu-kun [1 ]
Cui, Nai-qiang [2 ]
Zhuo, Yu-zhen [1 ]
Hu, Jian-gong [3 ]
Liu, Jun-hong [4 ]
Li, Di-hua [4 ]
Cui, Li-hua [1 ]
机构
[1] Tianjin Nankai Hosp, Inst Acute Abdominal Dis Integrated Tradit Chines, Dept Cell & Mol Biol, Tianjin 300100, Peoples R China
[2] Tianjin Nankai Hosp, Dept Biliary & Pancreat Surg 1, Tianjin 300100, Peoples R China
[3] Tianjin Univ Tradit Chinese Med, Liated Hosp 2, Dept Pathol, Tianjin 300150, Peoples R China
[4] Tianjin Nankai Hosp, Inst Acute Abdominal Dis Intergrated Tradit Chine, Dept Pharmacol, Tianjin 300100, Peoples R China
关键词
Modified Xiaochaihu Decoction; collagen degradation; chronic pancreatitis rats; matrix metalloproteinase 13; tissue inhibitor of metalloproteinase 1; MAD-RELATED PROTEINS; EXPRESSION;
D O I
10.1007/s11655-017-2413-0
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Objective To investigate the effect of Modified Xiaochaihu Decoction (MXD, (sic)& x5473;(sic)& x67f4;& x80e1;& x6c64;) on collagen degradation in rats with chronic pancreatitis (CP). Methods Rats were injected dibutyltin dichloride (DBTC, 7 mg/kg of body weight) into the right caudal vein to induce CP model. Thirty heallhy male Wistar rats were randomly divided into three groups by a random number table: the control, the model and the treatment groups. Rats of treatment group were administered MXD (10 g/kg of body weight) orally once daily starting from the day post-model establishment. Pancreatic tissues were harvested after 28-day feeding and fibrosis was evaluated by picro-sirius red staining. The contents of collagen type I and III were detected using enzymelinked immunosorbent assay (ELISA), the expression of matrix metalloproteinase 13 (MMP13) and tissue inhibitor of metalloproteinase 1 (TIMP1) was analyzed by Western blot and real-time polymerase chain reaction (PCR). Results The fibrosis scoring of pancreatic tissues, the concentrations of collagen type I and III, the expression levels of MMP13 and TIMP1 proteins and mRNA in the model group were all increased compared with the control group (P<0.05). After treatment with MXD, the fibrosis scoring of pancreatic tissues, the concentrations of collagen type I and III, the expression levels of MMP13 proteins and mRNA in the teatment group were all decreased compared with the model group (P<0.05), but there were no significant differences in the expression levels of TIMP1 proteins and mRNA (P>0.05). Conclusions MXD could promote collagen degradation and reverse pancreatic fibrosis in CP rats via a mechanism involve up-regulation of MMP13 expression.
引用
收藏
页码:599 / 603
页数:5
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