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Sasa veitchii extract protects against carbon tetrachloride-induced hepatic fibrosis in mice
BACKGROUND: The current study aimed to investigate the hepatoprotective effects of Sasa veitchii extract (SE) on carbon tetrachloride (CCl(4))-induced liver fibrosis in mice. METHODS: Male C57BL/6J mice were intraperitoneally injected with CCl(4) dissolved in olive oil (1 g/kg) twice per week for 8 ...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6190662/ https://www.ncbi.nlm.nih.gov/pubmed/30322375 http://dx.doi.org/10.1186/s12199-018-0739-7 |
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author | Yoshioka, Hiroki Nonogaki, Tsunemasa Fukaya, Shiori Ichimaru, Yoshimi Nagatsu, Akito Yoshikawa, Masae Fujii, Hirohisa Nakao, Makoto |
author_facet | Yoshioka, Hiroki Nonogaki, Tsunemasa Fukaya, Shiori Ichimaru, Yoshimi Nagatsu, Akito Yoshikawa, Masae Fujii, Hirohisa Nakao, Makoto |
author_sort | Yoshioka, Hiroki |
collection | PubMed |
description | BACKGROUND: The current study aimed to investigate the hepatoprotective effects of Sasa veitchii extract (SE) on carbon tetrachloride (CCl(4))-induced liver fibrosis in mice. METHODS: Male C57BL/6J mice were intraperitoneally injected with CCl(4) dissolved in olive oil (1 g/kg) twice per week for 8 weeks. SE (0.1 mL) was administered orally once per day throughout the study, and body weight was measured weekly. Seventy-two hours after the final CCl(4) injection, mice were euthanized and plasma samples were collected. The liver and kidneys were collected and weighed. RESULTS: CCl(4) administration increased liver weight, decreased body weight, elevated plasma alanine aminotransferase, and aspartate aminotransferase and increased liver oxidative stress (malondialdehyde and glutathione). These increases were attenuated by SE treatment. Overexpression of tumor necrosis factor-α was also reversed following SE treatment. Furthermore, CCl(4)-induced increases in α-smooth muscle actin, a marker for hepatic fibrosis, were attenuated in mice treated with SE. Moreover, SE inhibited CCl(4)-induced nuclear translocation of hepatic nuclear factor kappa B (NF-κB) p65 and phosphorylation of mitogen-activated protein kinase (MAPK). CONCLUSION: These results suggested that SE prevented CCl(4)-induced hepatic fibrosis by inhibiting the MAPK and NF-κB signaling pathways. |
format | Online Article Text |
id | pubmed-6190662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61906622018-10-22 Sasa veitchii extract protects against carbon tetrachloride-induced hepatic fibrosis in mice Yoshioka, Hiroki Nonogaki, Tsunemasa Fukaya, Shiori Ichimaru, Yoshimi Nagatsu, Akito Yoshikawa, Masae Fujii, Hirohisa Nakao, Makoto Environ Health Prev Med Research Article BACKGROUND: The current study aimed to investigate the hepatoprotective effects of Sasa veitchii extract (SE) on carbon tetrachloride (CCl(4))-induced liver fibrosis in mice. METHODS: Male C57BL/6J mice were intraperitoneally injected with CCl(4) dissolved in olive oil (1 g/kg) twice per week for 8 weeks. SE (0.1 mL) was administered orally once per day throughout the study, and body weight was measured weekly. Seventy-two hours after the final CCl(4) injection, mice were euthanized and plasma samples were collected. The liver and kidneys were collected and weighed. RESULTS: CCl(4) administration increased liver weight, decreased body weight, elevated plasma alanine aminotransferase, and aspartate aminotransferase and increased liver oxidative stress (malondialdehyde and glutathione). These increases were attenuated by SE treatment. Overexpression of tumor necrosis factor-α was also reversed following SE treatment. Furthermore, CCl(4)-induced increases in α-smooth muscle actin, a marker for hepatic fibrosis, were attenuated in mice treated with SE. Moreover, SE inhibited CCl(4)-induced nuclear translocation of hepatic nuclear factor kappa B (NF-κB) p65 and phosphorylation of mitogen-activated protein kinase (MAPK). CONCLUSION: These results suggested that SE prevented CCl(4)-induced hepatic fibrosis by inhibiting the MAPK and NF-κB signaling pathways. BioMed Central 2018-10-15 2018 /pmc/articles/PMC6190662/ /pubmed/30322375 http://dx.doi.org/10.1186/s12199-018-0739-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Yoshioka, Hiroki Nonogaki, Tsunemasa Fukaya, Shiori Ichimaru, Yoshimi Nagatsu, Akito Yoshikawa, Masae Fujii, Hirohisa Nakao, Makoto Sasa veitchii extract protects against carbon tetrachloride-induced hepatic fibrosis in mice |
title | Sasa veitchii extract protects against carbon tetrachloride-induced hepatic fibrosis in mice |
title_full | Sasa veitchii extract protects against carbon tetrachloride-induced hepatic fibrosis in mice |
title_fullStr | Sasa veitchii extract protects against carbon tetrachloride-induced hepatic fibrosis in mice |
title_full_unstemmed | Sasa veitchii extract protects against carbon tetrachloride-induced hepatic fibrosis in mice |
title_short | Sasa veitchii extract protects against carbon tetrachloride-induced hepatic fibrosis in mice |
title_sort | sasa veitchii extract protects against carbon tetrachloride-induced hepatic fibrosis in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6190662/ https://www.ncbi.nlm.nih.gov/pubmed/30322375 http://dx.doi.org/10.1186/s12199-018-0739-7 |
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