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Triptolide attenuates irritable bowel syndrome via inhibiting ODC1
BACKGROUND: Irritable bowel syndrome (IBS) is a chronic disorder of the gut-brain axis with significant morbidity. Triptolide, an active compound extracted from Tripterygium wilfordii Hook F (TwHF), has been widely used as a major medicinal herb in the treatment of inflammatory disease. METHODS: The...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10258977/ https://www.ncbi.nlm.nih.gov/pubmed/37308808 http://dx.doi.org/10.1186/s12876-023-02847-8 |
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author | Zhu, Ning Zhu, Liuyan Zhang, Xueliang Huang, Chengbin Xiang, Wenjun Huang, Bingwu |
author_facet | Zhu, Ning Zhu, Liuyan Zhang, Xueliang Huang, Chengbin Xiang, Wenjun Huang, Bingwu |
author_sort | Zhu, Ning |
collection | PubMed |
description | BACKGROUND: Irritable bowel syndrome (IBS) is a chronic disorder of the gut-brain axis with significant morbidity. Triptolide, an active compound extracted from Tripterygium wilfordii Hook F (TwHF), has been widely used as a major medicinal herb in the treatment of inflammatory disease. METHODS: The chronic-acute combined stress (CAS) stimulation was used to establish IBS rat model. The model rats were then gavaged with triptolide. Forced swimming, marble-burying, fecal weight and abdominal withdrawal reflex (AWR) score were recorded. Pathologic changes in the ileal and colonic tissues were validated by hematoxylin and eosin staining. The inflammatory cytokines and Ornithine Decarboxylase-1 (ODC1) in the ileal and colonic tissues were performed by ELISA and WB. RESULTS: Triptolide didn’t have antidepressant- and antianxiety- effects in rats caused by CAS, but decreased fecal weight and AWR score. In addition, Triptolide reduced the release of IL-1, IL-6, and TNF-α and the expression of ODC1 in the ileum and colon. CONCLUSION: The therapeutic efficacy of triptolide for IBS induced by CAS was revealed in this study, which may be related to the reduction of ODC1. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-023-02847-8. |
format | Online Article Text |
id | pubmed-10258977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102589772023-06-13 Triptolide attenuates irritable bowel syndrome via inhibiting ODC1 Zhu, Ning Zhu, Liuyan Zhang, Xueliang Huang, Chengbin Xiang, Wenjun Huang, Bingwu BMC Gastroenterol Research BACKGROUND: Irritable bowel syndrome (IBS) is a chronic disorder of the gut-brain axis with significant morbidity. Triptolide, an active compound extracted from Tripterygium wilfordii Hook F (TwHF), has been widely used as a major medicinal herb in the treatment of inflammatory disease. METHODS: The chronic-acute combined stress (CAS) stimulation was used to establish IBS rat model. The model rats were then gavaged with triptolide. Forced swimming, marble-burying, fecal weight and abdominal withdrawal reflex (AWR) score were recorded. Pathologic changes in the ileal and colonic tissues were validated by hematoxylin and eosin staining. The inflammatory cytokines and Ornithine Decarboxylase-1 (ODC1) in the ileal and colonic tissues were performed by ELISA and WB. RESULTS: Triptolide didn’t have antidepressant- and antianxiety- effects in rats caused by CAS, but decreased fecal weight and AWR score. In addition, Triptolide reduced the release of IL-1, IL-6, and TNF-α and the expression of ODC1 in the ileum and colon. CONCLUSION: The therapeutic efficacy of triptolide for IBS induced by CAS was revealed in this study, which may be related to the reduction of ODC1. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-023-02847-8. BioMed Central 2023-06-12 /pmc/articles/PMC10258977/ /pubmed/37308808 http://dx.doi.org/10.1186/s12876-023-02847-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhu, Ning Zhu, Liuyan Zhang, Xueliang Huang, Chengbin Xiang, Wenjun Huang, Bingwu Triptolide attenuates irritable bowel syndrome via inhibiting ODC1 |
title | Triptolide attenuates irritable bowel syndrome via inhibiting ODC1 |
title_full | Triptolide attenuates irritable bowel syndrome via inhibiting ODC1 |
title_fullStr | Triptolide attenuates irritable bowel syndrome via inhibiting ODC1 |
title_full_unstemmed | Triptolide attenuates irritable bowel syndrome via inhibiting ODC1 |
title_short | Triptolide attenuates irritable bowel syndrome via inhibiting ODC1 |
title_sort | triptolide attenuates irritable bowel syndrome via inhibiting odc1 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10258977/ https://www.ncbi.nlm.nih.gov/pubmed/37308808 http://dx.doi.org/10.1186/s12876-023-02847-8 |
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