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CCl(4)-Induced Liver Injury Was Ameliorated by Qi-Ge Decoction through the Antioxidant Pathway
Qi-Ge decoction (QGD), which is derived from the Huangqi Gegen decoction, contains three traditional Chinese herbs: Astragalus membranaceus (Huangqi), Pueraria lobata (Gegen), and Citri Reticulatae Blanco Pericarpium (Chenpi). Gastric mucosal damage caused by ethanol was prevented and alleviated by...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6955120/ https://www.ncbi.nlm.nih.gov/pubmed/31976000 http://dx.doi.org/10.1155/2019/5941263 |
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author | Peng, Chong Zhou, Zun-ming Li, Jing Luo, Yan Zhou, Yun-song Ke, Xue-hong Huang, Ke-er |
author_facet | Peng, Chong Zhou, Zun-ming Li, Jing Luo, Yan Zhou, Yun-song Ke, Xue-hong Huang, Ke-er |
author_sort | Peng, Chong |
collection | PubMed |
description | Qi-Ge decoction (QGD), which is derived from the Huangqi Gegen decoction, contains three traditional Chinese herbs: Astragalus membranaceus (Huangqi), Pueraria lobata (Gegen), and Citri Reticulatae Blanco Pericarpium (Chenpi). Gastric mucosal damage caused by ethanol was prevented and alleviated by QGD. However, the role of QGD in protecting the liver from toxins has not been reported. High-performance liquid chromatography with diode-array detection was used to qualitatively analyze QGD. Positive control (silymarin 100 mg/kg/day), QGD (20, 10, or 5 g/kg/day), and Nrf2 inhibitor brusatol (0.4 mg/kg/2 d) were administered to rats for 7 days, and then, liver injury was induced by injecting 2 mL/kg 25% CCl(4). After 24 h, blood and liver were collected for analysis and evaluation. QGD was found to contain 12 main components including calycosin, puerarin, and hesperidin. QGD treatment significantly reduced liver damage and decreased serum alanine aminotransferase, aspartate aminotransferase, and lactate dehydrogenase activities. QGD increased superoxide dismutase and catalase activities, and glutathione levels, but decreased malondialdehyde levels in livers from CCl(4)-treated rats. Compared to rats treated with CCl(4) alone, after QGD administration, mRNA and protein levels of nuclear factor erythroid 2-related factor 2 (Nrf2) and heme oxygenase-1 were increased, while those of Kelch-like ECH-related protein 1 (Keap1) and cytochrome P450 (CYP)2E1 were decreased. However, these improvements in QGD were reversed by brusatol. In conclusion, QGD can achieve its hepatoprotective effect through an antioxidant mechanism by activating the Nrf2 pathway. |
format | Online Article Text |
id | pubmed-6955120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-69551202020-01-23 CCl(4)-Induced Liver Injury Was Ameliorated by Qi-Ge Decoction through the Antioxidant Pathway Peng, Chong Zhou, Zun-ming Li, Jing Luo, Yan Zhou, Yun-song Ke, Xue-hong Huang, Ke-er Evid Based Complement Alternat Med Research Article Qi-Ge decoction (QGD), which is derived from the Huangqi Gegen decoction, contains three traditional Chinese herbs: Astragalus membranaceus (Huangqi), Pueraria lobata (Gegen), and Citri Reticulatae Blanco Pericarpium (Chenpi). Gastric mucosal damage caused by ethanol was prevented and alleviated by QGD. However, the role of QGD in protecting the liver from toxins has not been reported. High-performance liquid chromatography with diode-array detection was used to qualitatively analyze QGD. Positive control (silymarin 100 mg/kg/day), QGD (20, 10, or 5 g/kg/day), and Nrf2 inhibitor brusatol (0.4 mg/kg/2 d) were administered to rats for 7 days, and then, liver injury was induced by injecting 2 mL/kg 25% CCl(4). After 24 h, blood and liver were collected for analysis and evaluation. QGD was found to contain 12 main components including calycosin, puerarin, and hesperidin. QGD treatment significantly reduced liver damage and decreased serum alanine aminotransferase, aspartate aminotransferase, and lactate dehydrogenase activities. QGD increased superoxide dismutase and catalase activities, and glutathione levels, but decreased malondialdehyde levels in livers from CCl(4)-treated rats. Compared to rats treated with CCl(4) alone, after QGD administration, mRNA and protein levels of nuclear factor erythroid 2-related factor 2 (Nrf2) and heme oxygenase-1 were increased, while those of Kelch-like ECH-related protein 1 (Keap1) and cytochrome P450 (CYP)2E1 were decreased. However, these improvements in QGD were reversed by brusatol. In conclusion, QGD can achieve its hepatoprotective effect through an antioxidant mechanism by activating the Nrf2 pathway. Hindawi 2019-12-31 /pmc/articles/PMC6955120/ /pubmed/31976000 http://dx.doi.org/10.1155/2019/5941263 Text en Copyright © 2019 Chong Peng et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Peng, Chong Zhou, Zun-ming Li, Jing Luo, Yan Zhou, Yun-song Ke, Xue-hong Huang, Ke-er CCl(4)-Induced Liver Injury Was Ameliorated by Qi-Ge Decoction through the Antioxidant Pathway |
title | CCl(4)-Induced Liver Injury Was Ameliorated by Qi-Ge Decoction through the Antioxidant Pathway |
title_full | CCl(4)-Induced Liver Injury Was Ameliorated by Qi-Ge Decoction through the Antioxidant Pathway |
title_fullStr | CCl(4)-Induced Liver Injury Was Ameliorated by Qi-Ge Decoction through the Antioxidant Pathway |
title_full_unstemmed | CCl(4)-Induced Liver Injury Was Ameliorated by Qi-Ge Decoction through the Antioxidant Pathway |
title_short | CCl(4)-Induced Liver Injury Was Ameliorated by Qi-Ge Decoction through the Antioxidant Pathway |
title_sort | ccl(4)-induced liver injury was ameliorated by qi-ge decoction through the antioxidant pathway |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6955120/ https://www.ncbi.nlm.nih.gov/pubmed/31976000 http://dx.doi.org/10.1155/2019/5941263 |
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