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Beagle dog 90-day oral toxicity study of a novel coccidiostat – ethanamizuril
BACKGROUND: Triazine coccidiostats are widely used in chickens and turkeys for coccidiosis control. Ethanamizuril is a novel triazine compound that exhibits anticoccidial activity in poultry. This study was designed to evaluate the subchronic toxicity of ethanamizuril in beagle dogs at doses of 12,...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673092/ https://www.ncbi.nlm.nih.gov/pubmed/33203451 http://dx.doi.org/10.1186/s12917-020-02655-2 |
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author | Zhang, Keyu Zheng, Haihong Wei, Shuya Wang, Xiaoyang Fei, Chenzhong Wang, Chunmei Liu, Yingchun Zhang, Lifang Xue, Feiqun Tang, Shusheng |
author_facet | Zhang, Keyu Zheng, Haihong Wei, Shuya Wang, Xiaoyang Fei, Chenzhong Wang, Chunmei Liu, Yingchun Zhang, Lifang Xue, Feiqun Tang, Shusheng |
author_sort | Zhang, Keyu |
collection | PubMed |
description | BACKGROUND: Triazine coccidiostats are widely used in chickens and turkeys for coccidiosis control. Ethanamizuril is a novel triazine compound that exhibits anticoccidial activity in poultry. This study was designed to evaluate the subchronic toxicity of ethanamizuril in beagle dogs at doses of 12, 60 or 300 mg/kg/day in diet for 90 days. RESULTS: Ethanamizuril was well tolerated at low and middle dosages in beagle dogs, and no drug-related toxical effects were observaed in terms of survival, clinical observations, organs weight and damage in these dose groups. However, in high dose administration group, food consumption and histologic changes in kidneys were noticed in both sexes of beagle dog, although the renal lesions were finally resolved at the end of 4 weeks exposure of ethanamizuril. CONCLUSIONS: No-observed-adverse-effect level (NOAEL) was considered for ethanamizuril at dose of 60 mg/kg/day in Beagle dog. This result added toxicity effects of ethanamizuril to the safety database, which might guide safely using of ethanamizuril as a novel coccidiostat. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12917-020-02655-2. |
format | Online Article Text |
id | pubmed-7673092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76730922020-11-20 Beagle dog 90-day oral toxicity study of a novel coccidiostat – ethanamizuril Zhang, Keyu Zheng, Haihong Wei, Shuya Wang, Xiaoyang Fei, Chenzhong Wang, Chunmei Liu, Yingchun Zhang, Lifang Xue, Feiqun Tang, Shusheng BMC Vet Res Research Article BACKGROUND: Triazine coccidiostats are widely used in chickens and turkeys for coccidiosis control. Ethanamizuril is a novel triazine compound that exhibits anticoccidial activity in poultry. This study was designed to evaluate the subchronic toxicity of ethanamizuril in beagle dogs at doses of 12, 60 or 300 mg/kg/day in diet for 90 days. RESULTS: Ethanamizuril was well tolerated at low and middle dosages in beagle dogs, and no drug-related toxical effects were observaed in terms of survival, clinical observations, organs weight and damage in these dose groups. However, in high dose administration group, food consumption and histologic changes in kidneys were noticed in both sexes of beagle dog, although the renal lesions were finally resolved at the end of 4 weeks exposure of ethanamizuril. CONCLUSIONS: No-observed-adverse-effect level (NOAEL) was considered for ethanamizuril at dose of 60 mg/kg/day in Beagle dog. This result added toxicity effects of ethanamizuril to the safety database, which might guide safely using of ethanamizuril as a novel coccidiostat. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12917-020-02655-2. BioMed Central 2020-11-17 /pmc/articles/PMC7673092/ /pubmed/33203451 http://dx.doi.org/10.1186/s12917-020-02655-2 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 Zhang, Keyu Zheng, Haihong Wei, Shuya Wang, Xiaoyang Fei, Chenzhong Wang, Chunmei Liu, Yingchun Zhang, Lifang Xue, Feiqun Tang, Shusheng Beagle dog 90-day oral toxicity study of a novel coccidiostat – ethanamizuril |
title | Beagle dog 90-day oral toxicity study of a novel coccidiostat – ethanamizuril |
title_full | Beagle dog 90-day oral toxicity study of a novel coccidiostat – ethanamizuril |
title_fullStr | Beagle dog 90-day oral toxicity study of a novel coccidiostat – ethanamizuril |
title_full_unstemmed | Beagle dog 90-day oral toxicity study of a novel coccidiostat – ethanamizuril |
title_short | Beagle dog 90-day oral toxicity study of a novel coccidiostat – ethanamizuril |
title_sort | beagle dog 90-day oral toxicity study of a novel coccidiostat – ethanamizuril |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673092/ https://www.ncbi.nlm.nih.gov/pubmed/33203451 http://dx.doi.org/10.1186/s12917-020-02655-2 |
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