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The study of the Oxytropis kansuensis-induced apoptotic pathway in the cerebrum of SD rats
BACKGROUND: Locoweeds cause significant livestock poisoning and economic loss all over the world. Animals can develop locoism, a chronic neurological disease, after grazing on locoweeds. Oxytropis kansuensis is a variety of locoweed that contains swainsonine as its main toxic ingredient. The purpose...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015804/ https://www.ncbi.nlm.nih.gov/pubmed/24148892 http://dx.doi.org/10.1186/1746-6148-9-217 |
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author | Lu, Hao Zhang, Liang Wang, Shan-shan Wang, Wen-long Zhao, Bao-yu |
author_facet | Lu, Hao Zhang, Liang Wang, Shan-shan Wang, Wen-long Zhao, Bao-yu |
author_sort | Lu, Hao |
collection | PubMed |
description | BACKGROUND: Locoweeds cause significant livestock poisoning and economic loss all over the world. Animals can develop locoism, a chronic neurological disease, after grazing on locoweeds. Oxytropis kansuensis is a variety of locoweed that contains swainsonine as its main toxic ingredient. The purpose of this study was to investigate the apoptotic pathway induced in the cerebrum by swainsonine. RESULTS: Twenty-four Sprague-Dawley rats were randomly divided into four groups (experimental groups I, II, III and a control group) and 6 SD rats of each group were feed in 3 cages separately. Rats were penned as groups and fed with feeds containing 15% (SW content 0.03‰), 30% (SW content 0.06‰), or 45% (SW content 0.09‰) O. kansuensis for experimental groups I, II, and III, respectively, or complete feed in the case of the control group. One hundred and nineteen days after poisoning, and all rats showed neurological disorders at different degrees, which were considered to be successful established a chronic poisoning model of O. kansuensis. rats were sacrificed and the expression of Fas, FasL, Bcl-2, Bax as well as cleaved caspase-3, -8 and -9 proteins in brain tissues were detected by Western blot. The results showed that SW treatment up-regulated Fas and Fas ligand (FasL) (P < 0.05), and that there was an increase in Bax and a decrease in Bcl-2 protein (P < 0.01). Moreover, SW treatment significantly increases the activation of caspase-3, 8 and -9, the key effectors in apoptosis pathway (P < 0.01). CONCLUSION: Our data suggest that SW induces apoptosis in cells of the brain through death receptor and mitochondria-mediated, caspase-dependent apoptotic pathways in the brain tissue of SD rats. |
format | Online Article Text |
id | pubmed-4015804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40158042014-05-10 The study of the Oxytropis kansuensis-induced apoptotic pathway in the cerebrum of SD rats Lu, Hao Zhang, Liang Wang, Shan-shan Wang, Wen-long Zhao, Bao-yu BMC Vet Res Research Article BACKGROUND: Locoweeds cause significant livestock poisoning and economic loss all over the world. Animals can develop locoism, a chronic neurological disease, after grazing on locoweeds. Oxytropis kansuensis is a variety of locoweed that contains swainsonine as its main toxic ingredient. The purpose of this study was to investigate the apoptotic pathway induced in the cerebrum by swainsonine. RESULTS: Twenty-four Sprague-Dawley rats were randomly divided into four groups (experimental groups I, II, III and a control group) and 6 SD rats of each group were feed in 3 cages separately. Rats were penned as groups and fed with feeds containing 15% (SW content 0.03‰), 30% (SW content 0.06‰), or 45% (SW content 0.09‰) O. kansuensis for experimental groups I, II, and III, respectively, or complete feed in the case of the control group. One hundred and nineteen days after poisoning, and all rats showed neurological disorders at different degrees, which were considered to be successful established a chronic poisoning model of O. kansuensis. rats were sacrificed and the expression of Fas, FasL, Bcl-2, Bax as well as cleaved caspase-3, -8 and -9 proteins in brain tissues were detected by Western blot. The results showed that SW treatment up-regulated Fas and Fas ligand (FasL) (P < 0.05), and that there was an increase in Bax and a decrease in Bcl-2 protein (P < 0.01). Moreover, SW treatment significantly increases the activation of caspase-3, 8 and -9, the key effectors in apoptosis pathway (P < 0.01). CONCLUSION: Our data suggest that SW induces apoptosis in cells of the brain through death receptor and mitochondria-mediated, caspase-dependent apoptotic pathways in the brain tissue of SD rats. BioMed Central 2013-10-22 /pmc/articles/PMC4015804/ /pubmed/24148892 http://dx.doi.org/10.1186/1746-6148-9-217 Text en Copyright © 2013 Lu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lu, Hao Zhang, Liang Wang, Shan-shan Wang, Wen-long Zhao, Bao-yu The study of the Oxytropis kansuensis-induced apoptotic pathway in the cerebrum of SD rats |
title | The study of the Oxytropis kansuensis-induced apoptotic pathway in the cerebrum of SD rats |
title_full | The study of the Oxytropis kansuensis-induced apoptotic pathway in the cerebrum of SD rats |
title_fullStr | The study of the Oxytropis kansuensis-induced apoptotic pathway in the cerebrum of SD rats |
title_full_unstemmed | The study of the Oxytropis kansuensis-induced apoptotic pathway in the cerebrum of SD rats |
title_short | The study of the Oxytropis kansuensis-induced apoptotic pathway in the cerebrum of SD rats |
title_sort | study of the oxytropis kansuensis-induced apoptotic pathway in the cerebrum of sd rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015804/ https://www.ncbi.nlm.nih.gov/pubmed/24148892 http://dx.doi.org/10.1186/1746-6148-9-217 |
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