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Swertia cincta Burkill alleviates LPS/D-GalN-induced acute liver failure by modulating apoptosis and oxidative stress signaling pathways
Swertia cincta Burkill is widely distributed along the southwestern region of China. It is known as “Dida” in Tibetan and “Qingyedan” in Chinese medicine. It was used in folk medicine to treat hepatitis and other liver diseases. To understand how Swertia cincta Burkill extract (ESC) protects against...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333062/ https://www.ncbi.nlm.nih.gov/pubmed/37379130 http://dx.doi.org/10.18632/aging.204848 |
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author | Wu, Xinyan Zheng, Xiaomei Wen, Qiqi Zhang, Yang Tang, Huaqiao Zhao, Ling Shi, Fei Li, Yinglun Yin, Zhongqiong Zou, Yuanfeng Song, Xu Li, Lixia Zhao, Xinghong Ye, Gang |
author_facet | Wu, Xinyan Zheng, Xiaomei Wen, Qiqi Zhang, Yang Tang, Huaqiao Zhao, Ling Shi, Fei Li, Yinglun Yin, Zhongqiong Zou, Yuanfeng Song, Xu Li, Lixia Zhao, Xinghong Ye, Gang |
author_sort | Wu, Xinyan |
collection | PubMed |
description | Swertia cincta Burkill is widely distributed along the southwestern region of China. It is known as “Dida” in Tibetan and “Qingyedan” in Chinese medicine. It was used in folk medicine to treat hepatitis and other liver diseases. To understand how Swertia cincta Burkill extract (ESC) protects against acute liver failure (ALF), firstly, the active ingredients of ESC were identified using liquid chromatography-mass spectrometry (LC-MS), and further screening. Next, network pharmacology analyses were performed to identify the core targets of ESC against ALF and further determine the potential mechanisms. Finally, in vivo experiments as well as in vitro experiments were conducted for further validation. The results revealed that 72 potential targets of ESC were identified using target prediction. The core targets were ALB, ERBB2, AKT1, MMP9, EGFR, PTPRC, MTOR, ESR1, VEGFA, and HIF1A. Next, KEGG pathway analysis showed that EGFR and PI3K-AKT signaling pathways could have been involved in ESC against ALF. ESC exhibits hepatic protective functions via anti-inflammatory, antioxidant, and anti-apoptotic effects. Therefore, the EGFR-ERK, PI3K-AKT, and NRF2/HO-1 signaling pathways could participate in the therapeutic effects of ESC on ALF. |
format | Online Article Text |
id | pubmed-10333062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-103330622023-07-12 Swertia cincta Burkill alleviates LPS/D-GalN-induced acute liver failure by modulating apoptosis and oxidative stress signaling pathways Wu, Xinyan Zheng, Xiaomei Wen, Qiqi Zhang, Yang Tang, Huaqiao Zhao, Ling Shi, Fei Li, Yinglun Yin, Zhongqiong Zou, Yuanfeng Song, Xu Li, Lixia Zhao, Xinghong Ye, Gang Aging (Albany NY) Research Paper Swertia cincta Burkill is widely distributed along the southwestern region of China. It is known as “Dida” in Tibetan and “Qingyedan” in Chinese medicine. It was used in folk medicine to treat hepatitis and other liver diseases. To understand how Swertia cincta Burkill extract (ESC) protects against acute liver failure (ALF), firstly, the active ingredients of ESC were identified using liquid chromatography-mass spectrometry (LC-MS), and further screening. Next, network pharmacology analyses were performed to identify the core targets of ESC against ALF and further determine the potential mechanisms. Finally, in vivo experiments as well as in vitro experiments were conducted for further validation. The results revealed that 72 potential targets of ESC were identified using target prediction. The core targets were ALB, ERBB2, AKT1, MMP9, EGFR, PTPRC, MTOR, ESR1, VEGFA, and HIF1A. Next, KEGG pathway analysis showed that EGFR and PI3K-AKT signaling pathways could have been involved in ESC against ALF. ESC exhibits hepatic protective functions via anti-inflammatory, antioxidant, and anti-apoptotic effects. Therefore, the EGFR-ERK, PI3K-AKT, and NRF2/HO-1 signaling pathways could participate in the therapeutic effects of ESC on ALF. Impact Journals 2023-06-27 /pmc/articles/PMC10333062/ /pubmed/37379130 http://dx.doi.org/10.18632/aging.204848 Text en Copyright: © 2023 Wu et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Wu, Xinyan Zheng, Xiaomei Wen, Qiqi Zhang, Yang Tang, Huaqiao Zhao, Ling Shi, Fei Li, Yinglun Yin, Zhongqiong Zou, Yuanfeng Song, Xu Li, Lixia Zhao, Xinghong Ye, Gang Swertia cincta Burkill alleviates LPS/D-GalN-induced acute liver failure by modulating apoptosis and oxidative stress signaling pathways |
title | Swertia cincta Burkill alleviates LPS/D-GalN-induced acute liver failure by modulating apoptosis and oxidative stress signaling pathways |
title_full | Swertia cincta Burkill alleviates LPS/D-GalN-induced acute liver failure by modulating apoptosis and oxidative stress signaling pathways |
title_fullStr | Swertia cincta Burkill alleviates LPS/D-GalN-induced acute liver failure by modulating apoptosis and oxidative stress signaling pathways |
title_full_unstemmed | Swertia cincta Burkill alleviates LPS/D-GalN-induced acute liver failure by modulating apoptosis and oxidative stress signaling pathways |
title_short | Swertia cincta Burkill alleviates LPS/D-GalN-induced acute liver failure by modulating apoptosis and oxidative stress signaling pathways |
title_sort | swertia cincta burkill alleviates lps/d-galn-induced acute liver failure by modulating apoptosis and oxidative stress signaling pathways |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333062/ https://www.ncbi.nlm.nih.gov/pubmed/37379130 http://dx.doi.org/10.18632/aging.204848 |
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