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Sodium selenite prevents suppression of mucosal humoral response by AFB(1) in broiler’s cecal tonsil

Aflatoxin B(1) (AFB(1)), the most common mycotoxin in human food and animal feed, produces hepatotoxic, genotoxic and immunosuppressive effects in multiple species. Selenium (Se) has emerged as an important element in the dietary prevention of various toxic agents. The present study was designed to...

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Autores principales: Liu, Chunyu, Zuo, Zhicai, Zhu, Panpan, Zheng, Zhixiang, Peng, Xi, Fang, Jing, Cui, Hengmin, Zhou, Yi, Ouyang, Ping, Geng, Yi, Deng, Junliang, Sun, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589574/
https://www.ncbi.nlm.nih.gov/pubmed/28903335
http://dx.doi.org/10.18632/oncotarget.17105
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author Liu, Chunyu
Zuo, Zhicai
Zhu, Panpan
Zheng, Zhixiang
Peng, Xi
Fang, Jing
Cui, Hengmin
Zhou, Yi
Ouyang, Ping
Geng, Yi
Deng, Junliang
Sun, Yu
author_facet Liu, Chunyu
Zuo, Zhicai
Zhu, Panpan
Zheng, Zhixiang
Peng, Xi
Fang, Jing
Cui, Hengmin
Zhou, Yi
Ouyang, Ping
Geng, Yi
Deng, Junliang
Sun, Yu
author_sort Liu, Chunyu
collection PubMed
description Aflatoxin B(1) (AFB(1)), the most common mycotoxin in human food and animal feed, produces hepatotoxic, genotoxic and immunosuppressive effects in multiple species. Selenium (Se) has emerged as an important element in the dietary prevention of various toxic agents. The present study was designed to scrutinize the protective effects of sodium selenite on the histological lesions and suppression of mucosal humoral response in the cecal tonsil generated by AFB(1). A total of 156 one-day-old broilers were divided into four groups and fed on basal diet (control group), 0.6 mg/kg AFB(1) (AFB(1) group), 0.4 mg/kg Se supplement (+Se group), and 0.6 mg/kg AFB(1) + 0.4 mg/kg Se supplement (AFB(1)+Se group) respectively for 21 days. Our results showed that 0.4 mg/kg Se supplement in broiler's diets could improve the AFB(1)-induced histological lesions in the cecal tonsils including the depletion of lymphocytes in the lymphatic nodules as well as the shedding of microvilli in the absorptive cells. Moreover, Se could restore the decreased number of IgA+ cells and expression levels of pIgR, IgA, IgG, and IgM mRNA induced by AFB(1) to be close to those in the control group. These results demonstrated that 0.4 mg/kg supplemented dietary Se in the form of sodium selenite could protect the cecal tonsils from the histological lesions and suppression of the mucosal humoral response provoked by 0.6 mg/kg AFB(1). Our study may provide new experimental evidences for better understanding of AFB(1)-induced damage of mucosal immunity and protective effect of Se against this toxin.
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spelling pubmed-55895742017-09-12 Sodium selenite prevents suppression of mucosal humoral response by AFB(1) in broiler’s cecal tonsil Liu, Chunyu Zuo, Zhicai Zhu, Panpan Zheng, Zhixiang Peng, Xi Fang, Jing Cui, Hengmin Zhou, Yi Ouyang, Ping Geng, Yi Deng, Junliang Sun, Yu Oncotarget Research Paper Aflatoxin B(1) (AFB(1)), the most common mycotoxin in human food and animal feed, produces hepatotoxic, genotoxic and immunosuppressive effects in multiple species. Selenium (Se) has emerged as an important element in the dietary prevention of various toxic agents. The present study was designed to scrutinize the protective effects of sodium selenite on the histological lesions and suppression of mucosal humoral response in the cecal tonsil generated by AFB(1). A total of 156 one-day-old broilers were divided into four groups and fed on basal diet (control group), 0.6 mg/kg AFB(1) (AFB(1) group), 0.4 mg/kg Se supplement (+Se group), and 0.6 mg/kg AFB(1) + 0.4 mg/kg Se supplement (AFB(1)+Se group) respectively for 21 days. Our results showed that 0.4 mg/kg Se supplement in broiler's diets could improve the AFB(1)-induced histological lesions in the cecal tonsils including the depletion of lymphocytes in the lymphatic nodules as well as the shedding of microvilli in the absorptive cells. Moreover, Se could restore the decreased number of IgA+ cells and expression levels of pIgR, IgA, IgG, and IgM mRNA induced by AFB(1) to be close to those in the control group. These results demonstrated that 0.4 mg/kg supplemented dietary Se in the form of sodium selenite could protect the cecal tonsils from the histological lesions and suppression of the mucosal humoral response provoked by 0.6 mg/kg AFB(1). Our study may provide new experimental evidences for better understanding of AFB(1)-induced damage of mucosal immunity and protective effect of Se against this toxin. Impact Journals LLC 2017-04-13 /pmc/articles/PMC5589574/ /pubmed/28903335 http://dx.doi.org/10.18632/oncotarget.17105 Text en Copyright: © 2017 Liu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Liu, Chunyu
Zuo, Zhicai
Zhu, Panpan
Zheng, Zhixiang
Peng, Xi
Fang, Jing
Cui, Hengmin
Zhou, Yi
Ouyang, Ping
Geng, Yi
Deng, Junliang
Sun, Yu
Sodium selenite prevents suppression of mucosal humoral response by AFB(1) in broiler’s cecal tonsil
title Sodium selenite prevents suppression of mucosal humoral response by AFB(1) in broiler’s cecal tonsil
title_full Sodium selenite prevents suppression of mucosal humoral response by AFB(1) in broiler’s cecal tonsil
title_fullStr Sodium selenite prevents suppression of mucosal humoral response by AFB(1) in broiler’s cecal tonsil
title_full_unstemmed Sodium selenite prevents suppression of mucosal humoral response by AFB(1) in broiler’s cecal tonsil
title_short Sodium selenite prevents suppression of mucosal humoral response by AFB(1) in broiler’s cecal tonsil
title_sort sodium selenite prevents suppression of mucosal humoral response by afb(1) in broiler’s cecal tonsil
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589574/
https://www.ncbi.nlm.nih.gov/pubmed/28903335
http://dx.doi.org/10.18632/oncotarget.17105
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