Effect of Huangqin Tang on Colonic Gene Expression in Rats with Ulcerative Colitis

被引:8
|
作者
Wang, Dunfang [1 ]
Shi, KaiFeng [2 ]
Wang, Yanli [1 ]
Zou, Dixin [1 ]
Guo, Shanshan [1 ]
Li, Tao [3 ]
Xu, Hangyu [1 ]
Ma, Xuran [1 ]
Liu, JiaXing [1 ]
Song, HongXin [1 ]
Yang, Weipeng [1 ]
Li, Yu [4 ]
机构
[1] China Acad Chinese Med Sci, Inst Chinese Mat Med, Beijing 100700, Peoples R China
[2] China Acad Chinese Med Sci, Wang Jing Hosp, Beijing 100102, Peoples R China
[3] China Acad Chinese Med Sci, Expt Res Ctr, Beijing 100700, Peoples R China
[4] Beijing Univ Chinese Med, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
NF-KAPPA-B; SYNERGISTIC MECHANISM; CHEMICAL-CONSTITUENTS; PATHWAYS; ACID; RADIX; SCUTELLARIAE; BAICALEIN; PROFILES; FORMULA;
D O I
10.1155/2020/4238757
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we explored the pharmacological mechanisms of Huangqin Tang (HQT; a traditional Chinese medicine formula) in ulcerative colitis (UC) and provided evidence for potential roles HQT plays by gene expression profiling. The UC rat model was made via a compound method (trinitrobenzene sulfonic acid plus ethanol). After a ten-day treatment, microarray analysis was performed from the colon segment of the rats. Biological functions and specific signaling pathways were enriched based on differentially expressed genes (DEG), and corresponding gene networks were constructed via Ingenuity Pathway Analysis (IPA). Through the network, we screened the potential "candidate targets," such as ITGB1, FN1, CASP3, and ITGA5 and FABP1, ABCB1, FABP2, and SLC51B. These potential candidate targets were functionally related to immune responses, inflammation, and metabolism. Moreover, HQT significantly decreased serum levels of proinflammatory factors nitrogen monoxide (NO), proinflammatory cytokines interleukin- (IL-) 17, and prostaglandin E2 (PGE2). The degree of HE staining of colonic tissue was severe in the model group but reduced significantly in the HQT group. HQT exhibited protective effects against colon damage by inhibiting the inflammatory response.
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页数:10
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