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Treatment effect of a flavonoid prescription on duck virus hepatitis by its hepatoprotective and antioxidative ability
Context: Duck virus hepatitis (DVH) caused by duck hepatitis A virus type 1 (DHAV-1) is an acute and lethal disease of young ducklings. However, there is still no effective drug to treat DVH. Objective: This study assessed the curative effect on DVH of a flavonoid prescription baicalin-linarin-icari...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130485/ https://www.ncbi.nlm.nih.gov/pubmed/27927057 http://dx.doi.org/10.1080/13880209.2016.1255977 |
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author | Chen, Yun Zeng, Ling Lu, Yu Yang, Yulan Xu, Meiyun Wang, Yixuan Liu, Jiaguo |
author_facet | Chen, Yun Zeng, Ling Lu, Yu Yang, Yulan Xu, Meiyun Wang, Yixuan Liu, Jiaguo |
author_sort | Chen, Yun |
collection | PubMed |
description | Context: Duck virus hepatitis (DVH) caused by duck hepatitis A virus type 1 (DHAV-1) is an acute and lethal disease of young ducklings. However, there is still no effective drug to treat DVH. Objective: This study assessed the curative effect on DVH of a flavonoid prescription baicalin-linarin-icariin-notoginsenoside R1 (BLIN) as well as the hepatoprotective and antioxidative effects of BLIN. Materials and methods: MTT method was used to test the anti-DHAV-1 ability of BLIN in vitro. We then treated ducklings by BLIN (3 mg per duckling, once a day for 5 days) to evaluate the in vivo efficacy. To study the hepatoprotective and antioxidative roles of BLIN in its curative effect on DVH, we investigated the hepatic injury evaluation biomarkers and the oxidative stress evaluation indices of the ducklings. Results: On duck embryonic hepatocytes, DHAV-1 inhibitory rate of BLIN at 20 μg/mL was 69.3%. The survival rate of ducklings treated by BLIN was about 35.5%, which was significantly higher than that of virus control (0.0%). After the treatment of BLIN, both the hepatic injury and the oxidative stress of infected ducklings alleviated. At the same time, a significant positive correlation (p < 0.05) existed between the hepatic injury indices and the oxidative stress indices. Conclusions: BLIN showed a significant curative effect on DVH. The antioxidative and hepatoprotective effects of BLIN made great contributions to the treatment of DVH. Furthermore, BLIN is expected to be exploited as a new drug for the clinical treatment of DVH. |
format | Online Article Text |
id | pubmed-6130485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-61304852018-09-27 Treatment effect of a flavonoid prescription on duck virus hepatitis by its hepatoprotective and antioxidative ability Chen, Yun Zeng, Ling Lu, Yu Yang, Yulan Xu, Meiyun Wang, Yixuan Liu, Jiaguo Pharm Biol Research Article Context: Duck virus hepatitis (DVH) caused by duck hepatitis A virus type 1 (DHAV-1) is an acute and lethal disease of young ducklings. However, there is still no effective drug to treat DVH. Objective: This study assessed the curative effect on DVH of a flavonoid prescription baicalin-linarin-icariin-notoginsenoside R1 (BLIN) as well as the hepatoprotective and antioxidative effects of BLIN. Materials and methods: MTT method was used to test the anti-DHAV-1 ability of BLIN in vitro. We then treated ducklings by BLIN (3 mg per duckling, once a day for 5 days) to evaluate the in vivo efficacy. To study the hepatoprotective and antioxidative roles of BLIN in its curative effect on DVH, we investigated the hepatic injury evaluation biomarkers and the oxidative stress evaluation indices of the ducklings. Results: On duck embryonic hepatocytes, DHAV-1 inhibitory rate of BLIN at 20 μg/mL was 69.3%. The survival rate of ducklings treated by BLIN was about 35.5%, which was significantly higher than that of virus control (0.0%). After the treatment of BLIN, both the hepatic injury and the oxidative stress of infected ducklings alleviated. At the same time, a significant positive correlation (p < 0.05) existed between the hepatic injury indices and the oxidative stress indices. Conclusions: BLIN showed a significant curative effect on DVH. The antioxidative and hepatoprotective effects of BLIN made great contributions to the treatment of DVH. Furthermore, BLIN is expected to be exploited as a new drug for the clinical treatment of DVH. Taylor & Francis 2016-12-07 /pmc/articles/PMC6130485/ /pubmed/27927057 http://dx.doi.org/10.1080/13880209.2016.1255977 Text en © 2016 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/Licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/Licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chen, Yun Zeng, Ling Lu, Yu Yang, Yulan Xu, Meiyun Wang, Yixuan Liu, Jiaguo Treatment effect of a flavonoid prescription on duck virus hepatitis by its hepatoprotective and antioxidative ability |
title | Treatment effect of a flavonoid prescription on duck virus hepatitis by its hepatoprotective and antioxidative ability |
title_full | Treatment effect of a flavonoid prescription on duck virus hepatitis by its hepatoprotective and antioxidative ability |
title_fullStr | Treatment effect of a flavonoid prescription on duck virus hepatitis by its hepatoprotective and antioxidative ability |
title_full_unstemmed | Treatment effect of a flavonoid prescription on duck virus hepatitis by its hepatoprotective and antioxidative ability |
title_short | Treatment effect of a flavonoid prescription on duck virus hepatitis by its hepatoprotective and antioxidative ability |
title_sort | treatment effect of a flavonoid prescription on duck virus hepatitis by its hepatoprotective and antioxidative ability |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130485/ https://www.ncbi.nlm.nih.gov/pubmed/27927057 http://dx.doi.org/10.1080/13880209.2016.1255977 |
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