Mechanism Investigation of the Improvement of Chang Run Tong on the Colonic Remodeling in Streptozotocin-Induced Diabetic Rats

被引:5
|
作者
Sha, Hong [1 ]
Zhao, Dong [1 ]
Tong, Xiaolin [2 ]
Gregersen, Hans [3 ]
Zhao, Jingbo [3 ,4 ]
机构
[1] China Japan Hosp, Beijing 100029, Peoples R China
[2] China Acad Chinese Med Sci, Guanganmen Hosp, Beijing 100053, Peoples R China
[3] Chongqing Univ, Bioengn Coll, Chongqing 400044, Peoples R China
[4] Aarhus Univ, Dept Clin Med, DK-8200 Aarhus, Denmark
关键词
GLYCATION END-PRODUCTS; GROWTH-FACTOR-BETA; GASTROINTESTINAL COMPLICATIONS; TGF-BETA-1; EXPRESSION; EXTRACELLULAR-MATRIX; IGF-I; RECEPTOR; RAGE; CONSTIPATION; PATHWAY;
D O I
10.1155/2016/1826281
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Previous study demonstrated that Chang Run Tong (CRT) could partly restore the colon remodeling in streptozotocin- (STZ-) induced diabetic rats. Here we investigated the mechanisms of such effects of CRT. Diabetes was induced by a single injection of 40 mg/kg of STZ. CRT was poured into the stomach by gastric lavage once daily for 60 days. The remodeling parameters were obtained from diabetic (DM), CRT treated diabetic (T1, 50 g/kg; T2, 25 g/kg), and normal (Con) rats. Expressions of advanced glycation end product (AGE), AGE receptor, transforming growth factor-beta 1 (TGF-beta 1), and TGF-beta 1 receptor in the colon wall were immunochemically detected and quantitatively analyzed. The association between the expressions of those proteins and the remodeling parameters was analyzed. The expressions of those proteins were significantly higher in different colon layers in the DM group (P < 0.05, P < 0.01) and highly correlated to the remodeling parameters. Furthermore, the expressions of those proteins were significantly decreased in the T1 group (P < 0.05, P < 0.01) but not in the T2 group (P > 0.05). The corrective effect on the expressions of those proteins is likely to be one molecular pathway for the improvement of CRT on the diabetes-induced colon remodeling.
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页数:14
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