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Restenosis following balloon dilation of benign esophageal stenosis

机译:良性食管狭窄球囊扩张后的再狭窄

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AIM: To elucidate the mechanism of restenosis following balloon dilation of benign esophageal stenosis. METHODS: A total of 49 rats with esophageal stenosis were induced in 70 rats using 5 ml of 50 % sodium hydroxide solution and the double-balloon method, and an esophageal restenosis (RS) model was developed by esophageal stenosis using dilation of a percutaneous transluminal coronary angioplasty (PTCA) balloon catheter. These 49 rats were divided into two groups: rats with benign esophageal stricture caused by chemical burn only (control group, n=21) and rats with their esophageal stricture treated with balloon catheter dilation (experimental group, n=28). Imaging analysis and immunohistochemistry were used for both quantitative and qualitative analyses of esophageal stenosis and RS formation in the rats, respectively. RESULTS: Cross-sectional areas and perimeters of the esophageal mucosa layer, muscle layer, and the entire esophageal layers increased significantly in the experimental group compared with the control group. Proliferating cell nuclear antigen (PCNA) was expressed on the 5th day after dilation, and was still present at 1 month. Fibronectin (FN) was expressed on the 1st day after dilation, and was still present at 1 month. CONCLUSION: Expression of PCNA and FN plays an important role in RS after balloon dilation of benign esophageal stenosis.
机译:目的:阐明良性食管狭窄球囊扩张后再狭窄的机制。方法:采用5 ml 50%氢氧化钠溶液和双气囊法在70只大鼠中共诱发49只食管狭窄大鼠,并通过经皮腔内扩张术通过食管狭窄建立食管再狭窄(RS)模型。冠状动脉成形术(PTCA)球囊导管。这49只大鼠分为两组:仅由化学灼伤引起的良性食管狭窄大鼠(对照组,n = 21)和经球囊导管扩张治疗的食管狭窄大鼠(实验组,n = 28)。成像分析和免疫组织化学分别用于大鼠食管狭窄和RS形成的定量和定性分析。结果:与对照组相比,实验组的食管粘膜层,肌肉层和整个食管层的横截面积和周长明显增加。增殖细胞核抗原(PCNA)在扩张后的第5天表达,并在1个月时仍存在。纤连蛋白(FN)在扩张后的第一天表达,并在1个月时仍存在。结论:良性食管狭窄球囊扩张后,PCNA和FN的表达在RS中起重要作用。

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