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Efficacious rat model displays non-toxic effect with Korean beechwood creosote: a possible antibiotic substitute

Wood creosote, an herbal anti-diarrheal and a mixture of major volatile compounds, was tested for its non-toxicological effects, using a rat model, with the objective to use the creosote as an antibiotic substitute. A total of 30 Sprague-Dawley rats were studied to form five groups with 6 rats each....

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Autores principales: Quynh, Anh Nguyen Thai, Sharma, Neelesh, Cho, Kwang Keun, Yeo, Tae Jong, Kim, Ki Beom, Jeong, Chul Yon, Min, Tae Sun, Young, Kim Jae, Kim, Jin Nam, Jeong, Dong-Kee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433953/
https://www.ncbi.nlm.nih.gov/pubmed/26019530
http://dx.doi.org/10.1080/13102818.2014.931696
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author Quynh, Anh Nguyen Thai
Sharma, Neelesh
Cho, Kwang Keun
Yeo, Tae Jong
Kim, Ki Beom
Jeong, Chul Yon
Min, Tae Sun
Young, Kim Jae
Kim, Jin Nam
Jeong, Dong-Kee
author_facet Quynh, Anh Nguyen Thai
Sharma, Neelesh
Cho, Kwang Keun
Yeo, Tae Jong
Kim, Ki Beom
Jeong, Chul Yon
Min, Tae Sun
Young, Kim Jae
Kim, Jin Nam
Jeong, Dong-Kee
author_sort Quynh, Anh Nguyen Thai
collection PubMed
description Wood creosote, an herbal anti-diarrheal and a mixture of major volatile compounds, was tested for its non-toxicological effects, using a rat model, with the objective to use the creosote as an antibiotic substitute. A total of 30 Sprague-Dawley rats were studied to form five groups with 6 rats each. Korea beechwood creosote was supplemented into three test groups with 0.03 g/kg, 0.07 g/kg and 0.1 g/kg body weight/day without antibiotic support, along with a positive control of Apramycin sulphate (at 0.5% of the daily feed) and a negative control. Korean beechwood creosote supplementation showed no negative effect on the body weight gain in comparison to the negative and the positive control groups and the feed conversion ratio was also comparable with that of the control groups. The clinical pathology parameters studied were also under the umbrella of normal range, including liver specific enzymes, blood glucose, total protein, blood urea nitrogen (BUN), which indicated no toxic effect of creosote at the given doses. The non-hepatotoxic effect was also confirmed using hepatic damage specific molecular markers like Tim-p1, Tim-p2 and Tgf-β1. The results suggested that Korean beechwood may be used as antibiotic substitute in weanling pigs feed without any toxic effect on the body. Although the antimicrobial properties of creosote were not absolutely similar to those of apramycin sulphate, they were comparable.
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spelling pubmed-44339532015-05-25 Efficacious rat model displays non-toxic effect with Korean beechwood creosote: a possible antibiotic substitute Quynh, Anh Nguyen Thai Sharma, Neelesh Cho, Kwang Keun Yeo, Tae Jong Kim, Ki Beom Jeong, Chul Yon Min, Tae Sun Young, Kim Jae Kim, Jin Nam Jeong, Dong-Kee Biotechnol Biotechnol Equip Articles; Agriculture and Biotechnology Wood creosote, an herbal anti-diarrheal and a mixture of major volatile compounds, was tested for its non-toxicological effects, using a rat model, with the objective to use the creosote as an antibiotic substitute. A total of 30 Sprague-Dawley rats were studied to form five groups with 6 rats each. Korea beechwood creosote was supplemented into three test groups with 0.03 g/kg, 0.07 g/kg and 0.1 g/kg body weight/day without antibiotic support, along with a positive control of Apramycin sulphate (at 0.5% of the daily feed) and a negative control. Korean beechwood creosote supplementation showed no negative effect on the body weight gain in comparison to the negative and the positive control groups and the feed conversion ratio was also comparable with that of the control groups. The clinical pathology parameters studied were also under the umbrella of normal range, including liver specific enzymes, blood glucose, total protein, blood urea nitrogen (BUN), which indicated no toxic effect of creosote at the given doses. The non-hepatotoxic effect was also confirmed using hepatic damage specific molecular markers like Tim-p1, Tim-p2 and Tgf-β1. The results suggested that Korean beechwood may be used as antibiotic substitute in weanling pigs feed without any toxic effect on the body. Although the antimicrobial properties of creosote were not absolutely similar to those of apramycin sulphate, they were comparable. Taylor & Francis 2014-05-04 2014-07-10 /pmc/articles/PMC4433953/ /pubmed/26019530 http://dx.doi.org/10.1080/13102818.2014.931696 Text en © 2014 The Author(s). Published by Taylor & Francis. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Articles; Agriculture and Biotechnology
Quynh, Anh Nguyen Thai
Sharma, Neelesh
Cho, Kwang Keun
Yeo, Tae Jong
Kim, Ki Beom
Jeong, Chul Yon
Min, Tae Sun
Young, Kim Jae
Kim, Jin Nam
Jeong, Dong-Kee
Efficacious rat model displays non-toxic effect with Korean beechwood creosote: a possible antibiotic substitute
title Efficacious rat model displays non-toxic effect with Korean beechwood creosote: a possible antibiotic substitute
title_full Efficacious rat model displays non-toxic effect with Korean beechwood creosote: a possible antibiotic substitute
title_fullStr Efficacious rat model displays non-toxic effect with Korean beechwood creosote: a possible antibiotic substitute
title_full_unstemmed Efficacious rat model displays non-toxic effect with Korean beechwood creosote: a possible antibiotic substitute
title_short Efficacious rat model displays non-toxic effect with Korean beechwood creosote: a possible antibiotic substitute
title_sort efficacious rat model displays non-toxic effect with korean beechwood creosote: a possible antibiotic substitute
topic Articles; Agriculture and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433953/
https://www.ncbi.nlm.nih.gov/pubmed/26019530
http://dx.doi.org/10.1080/13102818.2014.931696
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