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化疗联合放疗诱导口腔黏膜炎大鼠模型。

A rat model against chemotherapy plus radiation-induced oral mucositis.

机构信息

Department of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal University, Manipal 576104, Karnataka, India.

出版信息

Saudi Pharm J. 2013 Oct;21(4):399-403. doi: 10.1016/j.jsps.2012.11.003.

Abstract

OBJECTIVES

Present study was aimed at developing an experimental model of oral mucositis in rats using a combination of chemotherapeutic agent and radiation.

STUDY DESIGN

Female Wistar rats (150-200 g) were divided into 3 groups (n = 6). Rats in group 1 (normal control) and group 2 (mucositis control) were treated with vehicle. Rats in group 3 were treated with l-glutamine (1 g/kg, p.o.; 15 days) before and after mucositis induction. Oral mucositis was induced by busulfan (6 mg/kg, p.o.; 4 days) and the tongue exposed to infrared (IR) radiation of intensity 40 mV/cm(2) for 5 s on the 1st, 4th and 10th days of challenge using a tail flick apparatus. Parameters monitored were body weight, food intake, blood count and survival. Oral mucositis score (OMS) was recorded daily. Histological changes of the irradiated tongue were assessed by hematoxylin and eosin staining.

RESULTS

Busulfan and IR radiation significantly reduced body weight and food intake of the mucositis control group as compared to normal control. Clear ulceration of the tongue reflected in the OMS. Histopathology of the tongue revealed intense lymphocytic infiltration, decreased thickness of squamous epithelial cell layer, decrease in number of blood vessels, and necrosis of cells along with pseudo-membrane formation in the mucositis control group. These findings suggested that oral mucositis was successfully induced and treatment with l-glutamine partially reversed these conditions.

CONCLUSION

Oral mucositis was established successfully in rats by the combination of chemotherapeutic agent and IR radiation. This may be a useful model for screening drugs in the treatment of oral mucositis.

摘要

目的

本研究旨在使用化疗药物和辐射联合建立大鼠口腔黏膜炎实验模型。

研究设计

将雌性 Wistar 大鼠(150-200g)分为 3 组(n=6)。第 1 组(正常对照组)和第 2 组(黏膜炎对照组)给予载体处理。第 3 组大鼠在口腔黏膜炎诱导前和诱导后给予 L-谷氨酰胺(1g/kg,po;15 天)。采用尾 flick 装置,用 6mg/kg 白消安(po;4 天)口服和 40mV/cm2 强度的红外(IR)辐射照射舌头,第 1、4 和 10 天各照射 5s,诱导口腔黏膜炎。监测的参数包括体重、摄食量、血常规和存活率。每天记录口腔黏膜炎评分(OMS)。采用苏木精和伊红染色评估受照射舌的组织学变化。

结果

与正常对照组相比,白消安和 IR 辐射显著降低了黏膜炎对照组的体重和摄食量。OMS 清楚地反映了舌的溃疡。舌组织病理学显示,黏膜炎对照组出现强烈的淋巴细胞浸润、鳞状上皮细胞层厚度降低、血管数量减少以及细胞坏死和伪膜形成。这些发现表明成功诱导了口腔黏膜炎,并且 L-谷氨酰胺治疗部分逆转了这些情况。

结论

通过化疗药物和 IR 辐射联合成功建立了大鼠口腔黏膜炎模型。这可能是筛选治疗口腔黏膜炎药物的有用模型。

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