...
首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Protective effects of Weipixiao decoction against MNNG-induced gastric precancerous lesions in rats
【24h】

Protective effects of Weipixiao decoction against MNNG-induced gastric precancerous lesions in rats

机译:WeiPixiao汤对大鼠Mnng诱导的胃癌癌前病变的保护作用

获取原文
获取原文并翻译 | 示例

摘要

Gastric cancer is recognized as one of the most common cancer. In-depth research of gastric precancerous lesions (GPL) plays an important role in preventing the occurrence of gastric cancer. Meanwhile, traditional treatment provides a novel sight in the prevention of occurrence and development of gastric cancer. The current study was designed to assess the effects of therapy with Weipixiao (WPX) decoction on N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced GPL rats and the underlying molecular mechanisms. After 10-weeks treatment, all rats were sacrificed. Histopathological changes of gastric tissue were assessed via hematoxylin-eosin (HE) and High-iron diamine-Alcian blue-Periodic acid-Schiff (HID-AB-PAS) staining. To be fully evidenced, RT-qPCR, Western blot and immunohistochemistry were used to detect the expressions of LDHA, CD147, HIF-1 alpha, MCT4, PI3K, AKT, mTOR and miRNA-34a, which were crucial factors for evaluating GPL in the aspect of glycolysis pathogenesis. According to the results of HE and HID-AB-PAS staining, it could be confirmed that MNNG-induced GPL rats were obviously reversed by WPX decoction. Additionally, the increased gene levels of LDHA, CD147, MCT4, PI3K, AKT, mTOR and HIF-1 alpha in model group were down-regulated by WPX decoction, while miRNA-34a expression was decreased and up-regulated by WPX decoction. The significantly increased protein levels of LDHA, CD147, MCT4, PI3K, AKT, mTOR and HIF-1 alpha induced by MNNG were attenuated in rats treated with WPX decoction. In brief, the findings of this study imply that abnormal glycolysis in MNNG-induced GPL rats was relieved by WPX decoction via regulation of the expressions of LDHA, CD147, HIF-1 alpha, MCT4, PI3K, AKT, mTOR and miRNA-34a.
机译:胃癌被认为是最常见的癌症之一。对胃癌癌前病变的深入研究(GPL)在预防胃癌的发生方面发挥着重要作用。与此同时,传统治疗在预防胃癌的发生和发展方面提供了一种新颖的景象。目前的研究旨在评估治疗对魏霞(WPX)汤对N-甲基-N'-硝基 - N-硝基胍(MNNG)的影响的影响,诱导的GPL大鼠和下面的分子机制。治疗10周后,牺牲了所有大鼠。通过苏木精 - 曙红(HE)和高铁二胺 - 阿里西蓝核酸 - 席夫(HID-AB-PAS)染色评估胃组织的组织病理学变化。为了完全证明,使用RT-QPCR,免疫印迹和免疫组织化学来检测LDHA,CD147,HIF-1α,MCT4,PI3K,AKT,MTOR和MIRNA-34A的表达,这是评估GPL中的关键因素糖酵解发病机制的方面。根据他和HID-AB-PAS染色的结果,可以证实MNNG诱导的GPL大鼠明显通过WPX煎剂逆转。另外,通过WPX煎剂对模型组的LDHA,CD147,MCT4,PI3K,AKT,MTOR和HIF-1α的增加的基因水平增加,而MiRNA-34A表达通过WPX煎剂降低和上调。在用WPX煎剂处理的大鼠中衰减了MNNG诱导的LDHA,CD147,MCT4,PI3K,AKT,MTOR和HIF-1α的显着增加的蛋白质水平。简而言之,本研究的发现意味着通过调节LDHA,CD147,HIF-1α,MCT4,PI3K,AKT,MTOR和MiRNA-34a的表达,通过调节WPX汤,通过调节WPX煎剂对MNNG诱导的GPL大鼠异常溶解。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号