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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 ...

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Autores principales: Yoshioka, Hiroki, Nonogaki, Tsunemasa, Fukaya, Shiori, Ichimaru, Yoshimi, Nagatsu, Akito, Yoshikawa, Masae, Fujii, Hirohisa, Nakao, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
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.
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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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