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Twenty-four-week oral dosing toxicities of Herba Siegesbeckiae in rats
BACKGROUND: Herba Siegesbeckiae (HS), the dried aerial parts of Siegesbeckia orientalis L., S. pubescens Makino, or S. glabrescens Makino, is traditionally used for treating chronic diseases in China. However, there is no information about the chronic toxicity of HS. The objective of this study is t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7661185/ https://www.ncbi.nlm.nih.gov/pubmed/33176782 http://dx.doi.org/10.1186/s12906-020-03137-6 |
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author | Wu, Jia-Ying Chan, Yuen-Cheung Guo, Hui Chen, Ying-Jie Liu, Yu-Xi Yi, Hua Yu, Zhi-Ling |
author_facet | Wu, Jia-Ying Chan, Yuen-Cheung Guo, Hui Chen, Ying-Jie Liu, Yu-Xi Yi, Hua Yu, Zhi-Ling |
author_sort | Wu, Jia-Ying |
collection | PubMed |
description | BACKGROUND: Herba Siegesbeckiae (HS), the dried aerial parts of Siegesbeckia orientalis L., S. pubescens Makino, or S. glabrescens Makino, is traditionally used for treating chronic diseases in China. However, there is no information about the chronic toxicity of HS. The objective of this study is to evaluate the 24-week oral dosing toxicities of HS aqueous extract (HSE) in rats. METHODS: S. orientalis-originated HS was reflux-extracted with distilled water. Sprague–Dawley rats were randomly divided into four groups, with 10 males and 10 females in each group. The rats were intragastrically administered with HSE at 5, 1.67 and 0.56 g/kg (experimental groups) or an equal volume of distilled water (control group), 6 days a week, for 24 weeks. The high dose of HSE (5 g/kg) was its maximum tolerated dose. Body weight was recorded every 2 days during the experimental period. Chemical, hematological and histopathological parameters, as well as organ weights, were measured at the end of the experiment. RESULTS: Decreased body weight gain; increased liver and lung relative weights; histopathological alterations in liver and lung tissues; elevated serum levels of alkaline phosphatase, aspartate aminotransferase, alanine aminotransferase and lactate dehydrogenase were found after HSE treatments. In liver tissues, HSE treatment upregulated levels of three pro-inflammatory cytokines: IL-6, IL-1β and TNF-α. In lung tissues, HSE treatment caused oxidative stress and activated mitogen-activated protein kinases (MAPKs). CONCLUSION: Long-term oral administration of HSE caused toxicities in rats evidenced by decreased body weight gain, as well as liver and lung damage. Treatment-induced oxidative stress, inflammation and MAPK activation are involved in HSE’s toxicities. Caution should be taken when using HS to treat chronic diseases. |
format | Online Article Text |
id | pubmed-7661185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76611852020-11-13 Twenty-four-week oral dosing toxicities of Herba Siegesbeckiae in rats Wu, Jia-Ying Chan, Yuen-Cheung Guo, Hui Chen, Ying-Jie Liu, Yu-Xi Yi, Hua Yu, Zhi-Ling BMC Complement Med Ther Research Article BACKGROUND: Herba Siegesbeckiae (HS), the dried aerial parts of Siegesbeckia orientalis L., S. pubescens Makino, or S. glabrescens Makino, is traditionally used for treating chronic diseases in China. However, there is no information about the chronic toxicity of HS. The objective of this study is to evaluate the 24-week oral dosing toxicities of HS aqueous extract (HSE) in rats. METHODS: S. orientalis-originated HS was reflux-extracted with distilled water. Sprague–Dawley rats were randomly divided into four groups, with 10 males and 10 females in each group. The rats were intragastrically administered with HSE at 5, 1.67 and 0.56 g/kg (experimental groups) or an equal volume of distilled water (control group), 6 days a week, for 24 weeks. The high dose of HSE (5 g/kg) was its maximum tolerated dose. Body weight was recorded every 2 days during the experimental period. Chemical, hematological and histopathological parameters, as well as organ weights, were measured at the end of the experiment. RESULTS: Decreased body weight gain; increased liver and lung relative weights; histopathological alterations in liver and lung tissues; elevated serum levels of alkaline phosphatase, aspartate aminotransferase, alanine aminotransferase and lactate dehydrogenase were found after HSE treatments. In liver tissues, HSE treatment upregulated levels of three pro-inflammatory cytokines: IL-6, IL-1β and TNF-α. In lung tissues, HSE treatment caused oxidative stress and activated mitogen-activated protein kinases (MAPKs). CONCLUSION: Long-term oral administration of HSE caused toxicities in rats evidenced by decreased body weight gain, as well as liver and lung damage. Treatment-induced oxidative stress, inflammation and MAPK activation are involved in HSE’s toxicities. Caution should be taken when using HS to treat chronic diseases. BioMed Central 2020-11-11 /pmc/articles/PMC7661185/ /pubmed/33176782 http://dx.doi.org/10.1186/s12906-020-03137-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Wu, Jia-Ying Chan, Yuen-Cheung Guo, Hui Chen, Ying-Jie Liu, Yu-Xi Yi, Hua Yu, Zhi-Ling Twenty-four-week oral dosing toxicities of Herba Siegesbeckiae in rats |
title | Twenty-four-week oral dosing toxicities of Herba Siegesbeckiae in rats |
title_full | Twenty-four-week oral dosing toxicities of Herba Siegesbeckiae in rats |
title_fullStr | Twenty-four-week oral dosing toxicities of Herba Siegesbeckiae in rats |
title_full_unstemmed | Twenty-four-week oral dosing toxicities of Herba Siegesbeckiae in rats |
title_short | Twenty-four-week oral dosing toxicities of Herba Siegesbeckiae in rats |
title_sort | twenty-four-week oral dosing toxicities of herba siegesbeckiae in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7661185/ https://www.ncbi.nlm.nih.gov/pubmed/33176782 http://dx.doi.org/10.1186/s12906-020-03137-6 |
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