Effects of Changtai granules, a traditional compound Chinese medicine, on chronic trinitrobenzene sulfonic acid-induced colitis in rats

被引:12
作者
Cao, Yong-Bing [1 ]
Zhang, Jun-Dong [1 ]
Diao, Ya-Ying [2 ]
Yan, Lan [1 ]
Wang, De-Jun [1 ]
Jia, Xin-Ming [1 ]
Gao, Ping-Hui [1 ]
Cheng, Ming-He [1 ]
Xu, Zheng [1 ]
Wang, Yan [1 ]
Jiang, Yuan-Ying [1 ]
机构
[1] Second Mil Med Univ, Dept Pharmacol, Sch Pharm, Shanghai 200433, Peoples R China
[2] Second Mil Med Univ, Changhai Hosp, Dept Pharm, Shanghai 200433, Peoples R China
关键词
Ulcerative colitis; Changtai granules; 2,4,6-Trinitrobenzene sulfonic acid; Myeloperoxidase;
D O I
10.3748/wjg.v11.i23.3539
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To study the effects of Changtai granules (CTG), a traditional compound Chinese medicine, on chronic trinitrobenzene sulfonic acid-induced colitis in rats. METHODS: Healthy adult Sprague-Dawley (SD) rats of both sexes, weighing 250-300 g, were employed in the present study. The rat colitis models were induced by 2, 4,6-trinitrobenzene sulfonic acid (TNBS) enemas at a concentration of 100 mg/kg in 50% ethanol. The experimental animals were randomly divided into dexamethasone (DX) treatment, CTG treatment, and model control groups, which were intracolicly treated daily with DX (0.2 mg/kg), CTG at doses of 2.9, 5.7 and 11.4 g crude drug/kg, and the equal amount of saline respectively from 6 h following induction of the colitis in rats inflicted with TNBS to the end of study. A normal control group of rats treated without TNBS but saline enema was also included in the study. After 3 wk of treatment, the animals were assessed for colonal inflammatory and ulcerative responses with respect to mortality, frequency of diarrhea, histology and myeloperoxidase activity (MPO). RESULTS: The therapeutic effect of CTG on ulcerative colitis (UC) was better than DX. CTG effectively inhibited the activity of granulocytes, macrophages and monocytes in a dose-dependent manner. Also it reduced MPO and formation of inflammation in colonic mucosal tissue. Furthermore, administration of CTG significantly prevented body mass loss and death, and decreased frequency of diarrhea in UC rats, when compared with the model control group rats. CONCLUSION: CTG would prove to be an ideal drug for chronic UC, and is warranted to be studied further. (C) 2005 The WJG Press and Elsevier Inc. All rights reserved.
引用
收藏
页码:3539 / 3543
页数:5
相关论文
共 33 条
[1]   Saccharomyces cerevisiae -: Associated diarrhea in an immunocompetent patient with ulcerative colitis [J].
Candelli, M ;
Nista, EC ;
Nestola, M ;
Armuzzi, A ;
Silveri, NG ;
Gasbarrini, G ;
Gasbarrini, A .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 2003, 36 (01) :39-40
[2]  
CAO YB, 2004, PHARM CARE RES, V4, P22
[3]  
Cheng W J, 2001, Zhongguo Zhong Xi Yi Jie He Za Zhi, V21, P34
[4]  
Cottone M, 1999, ITAL J GASTROENTEROL, V31, P503
[5]  
Delcò F, 1999, AM J GASTROENTEROL, V94, P2171
[6]   The genetics of inflammatory bowel disease [J].
Duerr, RH .
GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 2002, 31 (01) :63-+
[7]   Challenges in IBD research: Updating the scientific agendas [J].
Elson, CO ;
Sartor, RB ;
Targan, SR ;
Sandborn, WJ .
INFLAMMATORY BOWEL DISEASES, 2003, 9 (03) :137-153
[8]   Screening and surveillance colonoscopy in chronic Crohn's colitis [J].
Friedman, S ;
Rubin, PH ;
Bodian, C ;
Goldstein, E ;
Harpaz, N ;
Present, DH .
GASTROENTEROLOGY, 2001, 120 (04) :820-826
[9]   Systemic antibodies towards mucosal bacteria in ulcerative colitis and Crohn's disease differentially activate the innate immune response [J].
Furrie, E ;
Macfarlane, S ;
Cummings, JH ;
Macfarlane, GT .
GUT, 2004, 53 (01) :91-98
[10]   Etiology of the inflammatory bowel diseases [J].
Hugot, JP ;
Zouali, H ;
Lesage, S ;
Thomas, G .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 1999, 14 (01) :2-9