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Fucoidan partly prevents CCl(4)-induced liver fibrosis
Fucoidan, a sulfated polysaccharide extracted from brown algae, has a wide range of biological activities, including anti-inflammatory, anti-viral, and anti-tumor activities. In the present study, we investigated the effects of fucoidan on CCl(4)-induced liver fibrosis. Administration of fucoidan re...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2258315/ https://www.ncbi.nlm.nih.gov/pubmed/18068155 http://dx.doi.org/10.1016/j.ejphar.2007.11.015 |
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author | Hayashi, Shinji Itoh, Ayano Isoda, Katsuhiro Kondoh, Masuo Kawase, Masaya Yagi, Kiyohito |
author_facet | Hayashi, Shinji Itoh, Ayano Isoda, Katsuhiro Kondoh, Masuo Kawase, Masaya Yagi, Kiyohito |
author_sort | Hayashi, Shinji |
collection | PubMed |
description | Fucoidan, a sulfated polysaccharide extracted from brown algae, has a wide range of biological activities, including anti-inflammatory, anti-viral, and anti-tumor activities. In the present study, we investigated the effects of fucoidan on CCl(4)-induced liver fibrosis. Administration of fucoidan reduced CCl(4)-induced acute and chronic liver failure. Hepatic fibrosis induced by CCl(4) was also attenuated by injection of fucoidan. Damage to hepatocytes and activation of hepatic stellate cells are key events in liver fibrosis, and, interestingly, treatment of hepatocytes with fucoidan prevented CCl(4)-induced cell death and inhibited the proliferation hepatic stellate cells. These results indicate that fucoidan might be a promising anti-fibrotic agent possessing dual functions, namely, protection of hepatocytes and inhibition of hepatic stellate cell proliferation. |
format | Text |
id | pubmed-2258315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-22583152008-03-05 Fucoidan partly prevents CCl(4)-induced liver fibrosis Hayashi, Shinji Itoh, Ayano Isoda, Katsuhiro Kondoh, Masuo Kawase, Masaya Yagi, Kiyohito Eur J Pharmacol Article Fucoidan, a sulfated polysaccharide extracted from brown algae, has a wide range of biological activities, including anti-inflammatory, anti-viral, and anti-tumor activities. In the present study, we investigated the effects of fucoidan on CCl(4)-induced liver fibrosis. Administration of fucoidan reduced CCl(4)-induced acute and chronic liver failure. Hepatic fibrosis induced by CCl(4) was also attenuated by injection of fucoidan. Damage to hepatocytes and activation of hepatic stellate cells are key events in liver fibrosis, and, interestingly, treatment of hepatocytes with fucoidan prevented CCl(4)-induced cell death and inhibited the proliferation hepatic stellate cells. These results indicate that fucoidan might be a promising anti-fibrotic agent possessing dual functions, namely, protection of hepatocytes and inhibition of hepatic stellate cell proliferation. Elsevier Science 2008-02-12 /pmc/articles/PMC2258315/ /pubmed/18068155 http://dx.doi.org/10.1016/j.ejphar.2007.11.015 Text en © 2008 Elsevier B.V. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Hayashi, Shinji Itoh, Ayano Isoda, Katsuhiro Kondoh, Masuo Kawase, Masaya Yagi, Kiyohito Fucoidan partly prevents CCl(4)-induced liver fibrosis |
title | Fucoidan partly prevents CCl(4)-induced liver fibrosis |
title_full | Fucoidan partly prevents CCl(4)-induced liver fibrosis |
title_fullStr | Fucoidan partly prevents CCl(4)-induced liver fibrosis |
title_full_unstemmed | Fucoidan partly prevents CCl(4)-induced liver fibrosis |
title_short | Fucoidan partly prevents CCl(4)-induced liver fibrosis |
title_sort | fucoidan partly prevents ccl(4)-induced liver fibrosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2258315/ https://www.ncbi.nlm.nih.gov/pubmed/18068155 http://dx.doi.org/10.1016/j.ejphar.2007.11.015 |
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