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Toxicity Assessment of Cadinene Sesquiterpenes from Eupatorium adenophorum in Mice
This study evaluated toxic efficacy of Eupatorium adenophorum extracts, against the Kunming mice. In acute study, we firstly tested median lethal dose (LD(50)) in mice of three cadinene sesquiterpenes 2-deoxo-2-(acetyloxy)-9-oxoageraphorone (DAOA), 9-oxo-agerophorone (OA) and 9-oxo-10,11-dehydro-age...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327999/ https://www.ncbi.nlm.nih.gov/pubmed/25500813 http://dx.doi.org/10.1007/s13659-014-0050-2 |
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author | Ouyang, Can-Bin Liu, Xiao-Man Liu, Qi Bai, Jie Li, Hou-Yong Li, Yuan Wang, Qiu-Xia Yan, Dong-Dong Mao, Lian-Gang Cao, Aocheng Guo, Mei-Xia |
author_facet | Ouyang, Can-Bin Liu, Xiao-Man Liu, Qi Bai, Jie Li, Hou-Yong Li, Yuan Wang, Qiu-Xia Yan, Dong-Dong Mao, Lian-Gang Cao, Aocheng Guo, Mei-Xia |
author_sort | Ouyang, Can-Bin |
collection | PubMed |
description | This study evaluated toxic efficacy of Eupatorium adenophorum extracts, against the Kunming mice. In acute study, we firstly tested median lethal dose (LD(50)) in mice of three cadinene sesquiterpenes 2-deoxo-2-(acetyloxy)-9-oxoageraphorone (DAOA), 9-oxo-agerophorone (OA) and 9-oxo-10,11-dehydro-agerophorone (ODA) from Eupatorium adenophorum (Ea). DAOA (215–4640 mg/kg BW, given orally) showed lowest LD(50) at 926 mg/kg BW for male mice in contrast with OA (1470 mg/kg BW) and ODA (1470 mg/kg BW). In sub-acute study, repeated doses (75–300 mg/kg BW, for 7 days) of DAOA/OA increased blood parameters, liver and spleen index in dose dependent relationship, along with decrease in thymus index. The blood biochemical and histopathological examination showed that DAOA/OA dose 300 mg/kg BW significantly causes pathological changes of hepatic lobules and hepatocytes, which are consistent with cholestasis and hepatic injury. 75 mg/kg dose of DAOA/OA was found to be approximately/totally safe over the span of 7 days treatment showing no change in all above described parameters. Cadinene sesquiterpenes guarantee low risk to environment as a type of low toxic botanical components, which may find potential application in biopesticides development field. [Image: see text] |
format | Online Article Text |
id | pubmed-4327999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-43279992015-02-19 Toxicity Assessment of Cadinene Sesquiterpenes from Eupatorium adenophorum in Mice Ouyang, Can-Bin Liu, Xiao-Man Liu, Qi Bai, Jie Li, Hou-Yong Li, Yuan Wang, Qiu-Xia Yan, Dong-Dong Mao, Lian-Gang Cao, Aocheng Guo, Mei-Xia Nat Prod Bioprospect Original Article This study evaluated toxic efficacy of Eupatorium adenophorum extracts, against the Kunming mice. In acute study, we firstly tested median lethal dose (LD(50)) in mice of three cadinene sesquiterpenes 2-deoxo-2-(acetyloxy)-9-oxoageraphorone (DAOA), 9-oxo-agerophorone (OA) and 9-oxo-10,11-dehydro-agerophorone (ODA) from Eupatorium adenophorum (Ea). DAOA (215–4640 mg/kg BW, given orally) showed lowest LD(50) at 926 mg/kg BW for male mice in contrast with OA (1470 mg/kg BW) and ODA (1470 mg/kg BW). In sub-acute study, repeated doses (75–300 mg/kg BW, for 7 days) of DAOA/OA increased blood parameters, liver and spleen index in dose dependent relationship, along with decrease in thymus index. The blood biochemical and histopathological examination showed that DAOA/OA dose 300 mg/kg BW significantly causes pathological changes of hepatic lobules and hepatocytes, which are consistent with cholestasis and hepatic injury. 75 mg/kg dose of DAOA/OA was found to be approximately/totally safe over the span of 7 days treatment showing no change in all above described parameters. Cadinene sesquiterpenes guarantee low risk to environment as a type of low toxic botanical components, which may find potential application in biopesticides development field. [Image: see text] Springer Berlin Heidelberg 2014-12-12 /pmc/articles/PMC4327999/ /pubmed/25500813 http://dx.doi.org/10.1007/s13659-014-0050-2 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ This article is published under license to BioMed Central Ltd.Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Ouyang, Can-Bin Liu, Xiao-Man Liu, Qi Bai, Jie Li, Hou-Yong Li, Yuan Wang, Qiu-Xia Yan, Dong-Dong Mao, Lian-Gang Cao, Aocheng Guo, Mei-Xia Toxicity Assessment of Cadinene Sesquiterpenes from Eupatorium adenophorum in Mice |
title | Toxicity Assessment of Cadinene Sesquiterpenes from Eupatorium adenophorum in Mice |
title_full | Toxicity Assessment of Cadinene Sesquiterpenes from Eupatorium adenophorum in Mice |
title_fullStr | Toxicity Assessment of Cadinene Sesquiterpenes from Eupatorium adenophorum in Mice |
title_full_unstemmed | Toxicity Assessment of Cadinene Sesquiterpenes from Eupatorium adenophorum in Mice |
title_short | Toxicity Assessment of Cadinene Sesquiterpenes from Eupatorium adenophorum in Mice |
title_sort | toxicity assessment of cadinene sesquiterpenes from eupatorium adenophorum in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327999/ https://www.ncbi.nlm.nih.gov/pubmed/25500813 http://dx.doi.org/10.1007/s13659-014-0050-2 |
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