Effects of Weipixiao(胃痞消)on Wnt Pathway-Associated Proteins in Gastric Mucosal Epithelial Cells from Rats with Gastric Precancerous Lesions*  被引量:8

Effects of Weipixiao(胃痞消) on Wnt Pathway-Associated Proteins in Gastric Mucosal Epithelial Cells from Rats with Gastric Precancerous Lesions

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作  者:曾进浩 潘华峰 刘友章 徐海波 赵自明 李海文 任金玲 陈龙辉 胡霞 严艳 

机构地区:[1]The First Clinical Medical College,Guangzhou University of Chinese Medicine,Guangzhou(510405),China [2]Department of Pharmacology,Chengdu University of Traditional Chinese Medicine,Chengdu(611137),China [3]Guangdong Provincial Institute of Chinese Medicine,Guangzhou(510095),China

出  处:《Chinese Journal of Integrative Medicine》2016年第4期267-275,共9页中国结合医学杂志(英文版)

基  金:Supported by the National Natural Science Foundation of China(No.81273739)

摘  要:Objective: To study the effects of Weipixiao (胃痞消, WPX) on Wnt pathway-associated proteins in gastric mucosal epithelial cells from rats with gastric precancerous lesions (GPL). Methods: Sprague Dawley rats were randomly divided into control, model, vitacoenzyme (0.2 g·kg-l·day-1), WPX high-dose (H-WPX, 15 g·kg-l·day-1), WPX medium-dose (M-WPX, 7.5 g·kg-1·day-1) and WPX low-dose (L-WPX, 3.75 g·kg-l·day-1) groups. After successfully establishing the GPL model, the rats were consecutively administered WPX or vitacoenzyme by gastrogavage for 10 weeks. Differential expression of Leucine-rich repeat-containing G-protein- coupled receptor 5 (Lgr5), matrix metalloproteinase-7 (MMP-7), Wntl, Wnt3a, and 13 -catenin in gastric mucosal epithelial cells in all groups were immunohistochemically detected, and the images were taken and analyzed semiquantitatively by image pro plus 6.0 software. Results: Gastric epithelium in the model group showed significantly higher expression levels of Lgr5, MMP-7, Wntl, Wnt3a and 13 -catenin than those of the control group (P〈0.01). Interestingly, we also observed Lgr5+ cells, which generally located at the base of the gastric glandular unit, migrated to the luminal side of gastric epithelium with GPL. The expression levels of Lgr5, MMP-7, Wntl, and 13-catenin were all down-regulated in the L-WPX group as compared with those of both model and vitacoenzyme groups (P〈0.05). A similar, but nonsignificant down-regulation in expression level of Wnt3a was noted in all WPX groups (P〉0.05). Conclusion: Our findings suggested that the therapeutic mechanisms of WPX in treating GPL might be related with its inhibitory effects on the expressions of Lgr5, MMP-7, Wntl, β -catenin and the aberrant activation of Wnt/β -catenin pathway.Objective: To study the effects of Weipixiao (胃痞消, WPX) on Wnt pathway-associated proteins in gastric mucosal epithelial cells from rats with gastric precancerous lesions (GPL). Methods: Sprague Dawley rats were randomly divided into control, model, vitacoenzyme (0.2 g·kg-l·day-1), WPX high-dose (H-WPX, 15 g·kg-l·day-1), WPX medium-dose (M-WPX, 7.5 g·kg-1·day-1) and WPX low-dose (L-WPX, 3.75 g·kg-l·day-1) groups. After successfully establishing the GPL model, the rats were consecutively administered WPX or vitacoenzyme by gastrogavage for 10 weeks. Differential expression of Leucine-rich repeat-containing G-protein- coupled receptor 5 (Lgr5), matrix metalloproteinase-7 (MMP-7), Wntl, Wnt3a, and 13 -catenin in gastric mucosal epithelial cells in all groups were immunohistochemically detected, and the images were taken and analyzed semiquantitatively by image pro plus 6.0 software. Results: Gastric epithelium in the model group showed significantly higher expression levels of Lgr5, MMP-7, Wntl, Wnt3a and 13 -catenin than those of the control group (P〈0.01). Interestingly, we also observed Lgr5+ cells, which generally located at the base of the gastric glandular unit, migrated to the luminal side of gastric epithelium with GPL. The expression levels of Lgr5, MMP-7, Wntl, and 13-catenin were all down-regulated in the L-WPX group as compared with those of both model and vitacoenzyme groups (P〈0.05). A similar, but nonsignificant down-regulation in expression level of Wnt3a was noted in all WPX groups (P〉0.05). Conclusion: Our findings suggested that the therapeutic mechanisms of WPX in treating GPL might be related with its inhibitory effects on the expressions of Lgr5, MMP-7, Wntl, β -catenin and the aberrant activation of Wnt/β -catenin pathway.

关 键 词:gastric precancerous lesions Wnt/β-catenin pathway LGR5 matrix metalloproteinase-7 Wntl Wnt3a β -catenin Weipixiao Chinese medicine 

分 类 号:R285.5[医药卫生—中药学]

 

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