Mechanisms of indigo naturalis on treating ulcerative colitis explored by GEO gene chips combined with network pharmacology and molecular docking

被引:68
|
作者
Gu, Sizhen [1 ]
Xue, Yan [2 ]
Gao, Yang [1 ]
Shen, Shuyang [1 ]
Zhang, Yuli [1 ]
Chen, Kanjun [1 ]
Xue, Shigui [3 ]
Pan, Ji [3 ]
Tang, Yini [3 ]
Zhu, Hui [4 ]
Wu, Huan [1 ]
Dou, Danbo [1 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, Tradit Chinese Med Dept, 528 Zhang Heng Rd, Shanghai 201203, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, Shis Ctr Orthoped & Traumatol, Shanghai 201203, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, Digest Endoscopy Ctr, Shanghai 201203, Peoples R China
[4] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, Emergency Dept, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
INFLAMMATORY-BOWEL-DISEASE; ALTERNATIVE MEDICINE USE; CHINESE HERBAL MEDICINE; SULFATE-INDUCED COLITIS; TNBS-INDUCED COLITIS; BETA-SITOSTEROL; XILEI-SAN; QING-DAI; COMPLEMENTARY; EFFICACY;
D O I
10.1038/s41598-020-71030-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Oral administration of indigo naturalis (IN) can induce remission in ulcerative colitis (UC); however, the underlying mechanism remains unknown. The main active components and targets of IN were obtained by searching three traditional Chinese medicine network databases such as TCMSP and five Targets fishing databases such as PharmMapper. UC disease targets were obtained from three disease databases such as DrugBank,combined with four GEO gene chips. IN-UC targets were identified by matching the two. A protein-protein interaction network was constructed, and the core targets were screened according to the topological structure. GO and KEGG enrichment analysis and bioGPS localization were performed,and an Herbs-Components-Targets network, a Compound Targets-Organs location network, and a Core Targets-Signal Pathways network were established. Molecular docking technology was used to verify the main compounds-targets. Ten core active components and 184 compound targets of IN-UC, of which 43 were core targets, were enriched and analyzed by bioGPS, GO, and KEGG. The therapeutic effect of IN on UC may involve activation of systemic immunity, which is involved in the regulation of nuclear transcription, protein phosphorylation, cytokine activity, reactive oxygen metabolism, epithelial cell proliferation, and cell apoptosis through Th17 cell differentiation, the Jak-STAT and IL-17 signaling pathways, toll-like and NOD-like receptors, and other cellular and innate immune signaling pathways. The molecular mechanism underlying the effect of IN on inducing UC remission was predicted using a network pharmacology method, thereby providing a theoretical basis for further study of the effective components and mechanism of IN in the treatment of UC.
引用
收藏
页数:17
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