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

机译:常润通改善链脲佐菌素诱导的糖尿病大鼠结肠重塑的机制研究

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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-β1 (TGF-β1), and TGF-β1 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.
机译:先前的研究表明,Chang Run Tong(CRT)可以部分恢复链脲佐菌素(STZ-)诱导的糖尿病大鼠的结肠重塑。在这里,我们研究了这种CRT影响的机制。糖尿病是通过单次注射40 µmg / kg的STZ诱导的。每天一次通过洗胃将CRT倒入胃中60天。从糖尿病(DM),经CRT治疗的糖尿病(T1,50μg/ kg; T2,25μg/ kg)和正常(Con)大鼠获得重塑参数。免疫化学检测并定量分析了结肠壁中晚期糖基化终产物(AGE),AGE受体,转化生长因子-β1(TGF-β1)和TGF-β1受体的表达。分析了这些蛋白质的表达与重塑参数之间的关联。 DM组不同结肠层中这些蛋白的表达明显较高(P <0.05,P <0.01),并且与重塑参数高度相关。此外,这些蛋白的表达在T1组中显着降低(P <0.05,P <0.01),而在T2组中则没有显着降低(P> 0.05)。对那些蛋白质表达的纠正作用可能是改善CRT对糖尿病引起的结肠重塑的分子途径。

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