Cargando…

Identification of Active Compounds and Mechanism of Huangtu Decoction for the Treatment of Ulcerative Colitis by Network Pharmacology Combined with Experimental Verification

INTRODUCTION: Huangtu decoction (HTD) has been widely used in the treatment of gastrointestinal bleeding, ulcerative colitis (UC) and gastrointestinal tumors in China, but its active compounds and mechanism are still not clear yet. The present research aimed to identify the active compounds and mech...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Wenwen, He, Lin, Zhong, Lian, Sun, Jiayi, Zhang, Lilin, Wei, Daneng, Wu, Chunjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487861/
https://www.ncbi.nlm.nih.gov/pubmed/34616145
http://dx.doi.org/10.2147/DDDT.S328333
_version_ 1784578044974858240
author Chen, Wenwen
He, Lin
Zhong, Lian
Sun, Jiayi
Zhang, Lilin
Wei, Daneng
Wu, Chunjie
author_facet Chen, Wenwen
He, Lin
Zhong, Lian
Sun, Jiayi
Zhang, Lilin
Wei, Daneng
Wu, Chunjie
author_sort Chen, Wenwen
collection PubMed
description INTRODUCTION: Huangtu decoction (HTD) has been widely used in the treatment of gastrointestinal bleeding, ulcerative colitis (UC) and gastrointestinal tumors in China, but its active compounds and mechanism are still not clear yet. The present research aimed to identify the active compounds and mechanism of HTD for the treatment of UC. METHODS: Firstly, the chemical compounds of HTD were qualitatively identified based on Q Exactive Orbitrap LC-MS/MS, and their potential targets were predicted through SwissTargetPrediction. Secondly, the differential expressed genes (DEGs) in colon tissues of UC patients and normal controls were retrieved from the GEO database. Thirdly, the overlapping targets of DEGs and the predicted targets were obtained and subjected to GO and KEGG analysis. Finally, the key targets in the most significantly enriched pathway were verified by in vivo experiment, and the protein and mRNA expressions of matrix metalloproteinase-1 (MMP1), MMP3, MMP7, MMP9 and MMP12 were determined by immunohistochemistry (IHC), Western blotting (WB) and quantitative real-time-PCR (qRT-PCR). RESULTS: A total of 47 compounds were identified and 29 overlapping targets were obtained from HTD extract. The most significantly enriched pathway of overlapping targets involved was MMP. HTD improved the pathological damage in colon tissues of DSS-induced UC model and significantly decreased the serum levels of IL-1β and IL-6. The protein and mRNA expressions of MMP1, MMP3 and MMP9 in colon tissues were significantly decreased after HTD treatment. CONCLUSION: HTD treatment can alleviate the colonic inflammation via inhibiting MMPs including MMP1, MMP3 and MMP9.
format Online
Article
Text
id pubmed-8487861
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-84878612021-10-05 Identification of Active Compounds and Mechanism of Huangtu Decoction for the Treatment of Ulcerative Colitis by Network Pharmacology Combined with Experimental Verification Chen, Wenwen He, Lin Zhong, Lian Sun, Jiayi Zhang, Lilin Wei, Daneng Wu, Chunjie Drug Des Devel Ther Original Research INTRODUCTION: Huangtu decoction (HTD) has been widely used in the treatment of gastrointestinal bleeding, ulcerative colitis (UC) and gastrointestinal tumors in China, but its active compounds and mechanism are still not clear yet. The present research aimed to identify the active compounds and mechanism of HTD for the treatment of UC. METHODS: Firstly, the chemical compounds of HTD were qualitatively identified based on Q Exactive Orbitrap LC-MS/MS, and their potential targets were predicted through SwissTargetPrediction. Secondly, the differential expressed genes (DEGs) in colon tissues of UC patients and normal controls were retrieved from the GEO database. Thirdly, the overlapping targets of DEGs and the predicted targets were obtained and subjected to GO and KEGG analysis. Finally, the key targets in the most significantly enriched pathway were verified by in vivo experiment, and the protein and mRNA expressions of matrix metalloproteinase-1 (MMP1), MMP3, MMP7, MMP9 and MMP12 were determined by immunohistochemistry (IHC), Western blotting (WB) and quantitative real-time-PCR (qRT-PCR). RESULTS: A total of 47 compounds were identified and 29 overlapping targets were obtained from HTD extract. The most significantly enriched pathway of overlapping targets involved was MMP. HTD improved the pathological damage in colon tissues of DSS-induced UC model and significantly decreased the serum levels of IL-1β and IL-6. The protein and mRNA expressions of MMP1, MMP3 and MMP9 in colon tissues were significantly decreased after HTD treatment. CONCLUSION: HTD treatment can alleviate the colonic inflammation via inhibiting MMPs including MMP1, MMP3 and MMP9. Dove 2021-09-29 /pmc/articles/PMC8487861/ /pubmed/34616145 http://dx.doi.org/10.2147/DDDT.S328333 Text en © 2021 Chen et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Chen, Wenwen
He, Lin
Zhong, Lian
Sun, Jiayi
Zhang, Lilin
Wei, Daneng
Wu, Chunjie
Identification of Active Compounds and Mechanism of Huangtu Decoction for the Treatment of Ulcerative Colitis by Network Pharmacology Combined with Experimental Verification
title Identification of Active Compounds and Mechanism of Huangtu Decoction for the Treatment of Ulcerative Colitis by Network Pharmacology Combined with Experimental Verification
title_full Identification of Active Compounds and Mechanism of Huangtu Decoction for the Treatment of Ulcerative Colitis by Network Pharmacology Combined with Experimental Verification
title_fullStr Identification of Active Compounds and Mechanism of Huangtu Decoction for the Treatment of Ulcerative Colitis by Network Pharmacology Combined with Experimental Verification
title_full_unstemmed Identification of Active Compounds and Mechanism of Huangtu Decoction for the Treatment of Ulcerative Colitis by Network Pharmacology Combined with Experimental Verification
title_short Identification of Active Compounds and Mechanism of Huangtu Decoction for the Treatment of Ulcerative Colitis by Network Pharmacology Combined with Experimental Verification
title_sort identification of active compounds and mechanism of huangtu decoction for the treatment of ulcerative colitis by network pharmacology combined with experimental verification
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487861/
https://www.ncbi.nlm.nih.gov/pubmed/34616145
http://dx.doi.org/10.2147/DDDT.S328333
work_keys_str_mv AT chenwenwen identificationofactivecompoundsandmechanismofhuangtudecoctionforthetreatmentofulcerativecolitisbynetworkpharmacologycombinedwithexperimentalverification
AT helin identificationofactivecompoundsandmechanismofhuangtudecoctionforthetreatmentofulcerativecolitisbynetworkpharmacologycombinedwithexperimentalverification
AT zhonglian identificationofactivecompoundsandmechanismofhuangtudecoctionforthetreatmentofulcerativecolitisbynetworkpharmacologycombinedwithexperimentalverification
AT sunjiayi identificationofactivecompoundsandmechanismofhuangtudecoctionforthetreatmentofulcerativecolitisbynetworkpharmacologycombinedwithexperimentalverification
AT zhanglilin identificationofactivecompoundsandmechanismofhuangtudecoctionforthetreatmentofulcerativecolitisbynetworkpharmacologycombinedwithexperimentalverification
AT weidaneng identificationofactivecompoundsandmechanismofhuangtudecoctionforthetreatmentofulcerativecolitisbynetworkpharmacologycombinedwithexperimentalverification
AT wuchunjie identificationofactivecompoundsandmechanismofhuangtudecoctionforthetreatmentofulcerativecolitisbynetworkpharmacologycombinedwithexperimentalverification