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白芍口服液复方通过表皮生长因子(EGF)和转化生长因子-β1(TGF-β1)表达对放射性食管毒性的治疗作用

Therapeutic effect of compound of White Peony Root Oral Liquids on radiation-induced esophageal toxicity via the expression of EGF and TGF-β1.

作者信息

Shen Li, Li Xing, Shan Baoen, Zhang Li, Gong Yanjun, Dong Zhiming, Wang Zhiyu

机构信息

Department of Internal Medicine, The First Hospital of the Hebei Medical University, Shijiazhuang, Hebei 050031;

Department of Biotherapy, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei 050011;

出版信息

Biomed Rep. 2013 Mar;1(2):308-314. doi: 10.3892/br.2012.51. Epub 2012 Dec 21.

Abstract

The predominant pathological processes of radiation-induced esophageal toxicity include inflammatory reactions in the early stage and the fibrotic process in the late stage. An increased expression of the epidermal growth factor (EGF) and transforming growth factor β1 (TGF-β1) is capable of reducing inflammatory reactions and TGF-β1 is considered responsible for the initiation, development and persistence of fibrosis. In the present study, we investigated the therapeutic effect of the compound of white peony root oral liquids (cWPROL) on reducing the toxicity via modulating the expression levels of EGF and TGF-β1. Adult male Wistar rats were treated and tissue sections were obtained. The tissue sections were stained using histological, Masson and immunohistochemical staining. The results revealed that cWPROL had a higher rate of repairing damaged structures compared with the control group. In addition, immunohistochemistry showed that although cWPROL and the mixture of lidocaine, dexamethasone and gentamycin (mLDG) induced levels of EGF and TGF-β1 expression, there were differences between the two types of intervention. These results are significant for understanding that the mechanism of therapeutic effect of cWPROL varied to some extent from that of mLDG.

摘要

放射性食管炎的主要病理过程包括早期的炎症反应和晚期的纤维化过程。表皮生长因子(EGF)和转化生长因子β1(TGF-β1)表达增加能够减轻炎症反应,且TGF-β1被认为与纤维化的起始、发展和持续有关。在本研究中,我们研究了白芍根口服液复合物(cWPROL)通过调节EGF和TGF-β1表达水平来减轻毒性的治疗效果。对成年雄性Wistar大鼠进行处理并获取组织切片。使用组织学、Masson和免疫组织化学染色对组织切片进行染色。结果显示,与对照组相比,cWPROL对受损结构的修复率更高。此外,免疫组织化学显示,尽管cWPROL和利多卡因、地塞米松与庆大霉素混合物(mLDG)均可诱导EGF和TGF-β1表达水平,但两种干预类型之间存在差异。这些结果对于理解cWPROL的治疗作用机制在一定程度上与mLDG不同具有重要意义。

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