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Histopathological Injuries, Ultrastructural Changes, and Depressed TLR Expression in the Small Intestine of Broiler Chickens with Aflatoxin B(1)

To explore AFB(1)-induced damage of the small intestine, the changes in structure and expression of TLRs (Toll-like Receptors) in the small intestine of chickens were systematically investigated. Ninety healthy neonatal Cobb chickens were randomized into a control group (0 mg/kg AFB(1)) and an AFB(1...

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Autores principales: Wang, Fengyuan, Zuo, Zhicai, Chen, Kejie, Gao, Caixia, Yang, Zhuangzhi, Zhao, Song, Li, Jianzhen, Song, Hetao, Peng, Xi, Fang, Jing, Cui, Hengmin, Ouyang, Ping, Zhou, Yi, Shu, Gang, Jing, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923297/
https://www.ncbi.nlm.nih.gov/pubmed/29561786
http://dx.doi.org/10.3390/toxins10040131
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author Wang, Fengyuan
Zuo, Zhicai
Chen, Kejie
Gao, Caixia
Yang, Zhuangzhi
Zhao, Song
Li, Jianzhen
Song, Hetao
Peng, Xi
Fang, Jing
Cui, Hengmin
Ouyang, Ping
Zhou, Yi
Shu, Gang
Jing, Bo
author_facet Wang, Fengyuan
Zuo, Zhicai
Chen, Kejie
Gao, Caixia
Yang, Zhuangzhi
Zhao, Song
Li, Jianzhen
Song, Hetao
Peng, Xi
Fang, Jing
Cui, Hengmin
Ouyang, Ping
Zhou, Yi
Shu, Gang
Jing, Bo
author_sort Wang, Fengyuan
collection PubMed
description To explore AFB(1)-induced damage of the small intestine, the changes in structure and expression of TLRs (Toll-like Receptors) in the small intestine of chickens were systematically investigated. Ninety healthy neonatal Cobb chickens were randomized into a control group (0 mg/kg AFB(1)) and an AFB(1) group (0.6 mg/kg AFB(1)). The crypt depth of the small intestine in the AFB(1) group was significantly increased in comparison to the control chickens, while the villus height and area were evidently decreased, as well as the villus:crypt ratio and epithelial thickness. The histopathological observations showed that the villi of the small intestine exposed to AFB(1) were obviously shedding. Based on ultrastructural observation, the absorptive cells of small intestine in the AFB(1) group exhibited fewer microvilli, mitochondrial vacuolation and the disappearance of mitochondrial cristae, and junctional complexes as well as terminal web. Moreover, the number of goblet cells in the small intestine in the AFB(1) group significantly decreased. Also, AFB(1) evidently decreased the mRNA expression of TLR2-2, TLR4, and TLR7 in the small intestine. Taken together, our study indicated that dietary 0.6 mg/kg AFB(1) could induce histopathological injuries and ultrastructural changes, and depress levels of TLR mRNA in the chicken small intestine.
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spelling pubmed-59232972018-05-03 Histopathological Injuries, Ultrastructural Changes, and Depressed TLR Expression in the Small Intestine of Broiler Chickens with Aflatoxin B(1) Wang, Fengyuan Zuo, Zhicai Chen, Kejie Gao, Caixia Yang, Zhuangzhi Zhao, Song Li, Jianzhen Song, Hetao Peng, Xi Fang, Jing Cui, Hengmin Ouyang, Ping Zhou, Yi Shu, Gang Jing, Bo Toxins (Basel) Article To explore AFB(1)-induced damage of the small intestine, the changes in structure and expression of TLRs (Toll-like Receptors) in the small intestine of chickens were systematically investigated. Ninety healthy neonatal Cobb chickens were randomized into a control group (0 mg/kg AFB(1)) and an AFB(1) group (0.6 mg/kg AFB(1)). The crypt depth of the small intestine in the AFB(1) group was significantly increased in comparison to the control chickens, while the villus height and area were evidently decreased, as well as the villus:crypt ratio and epithelial thickness. The histopathological observations showed that the villi of the small intestine exposed to AFB(1) were obviously shedding. Based on ultrastructural observation, the absorptive cells of small intestine in the AFB(1) group exhibited fewer microvilli, mitochondrial vacuolation and the disappearance of mitochondrial cristae, and junctional complexes as well as terminal web. Moreover, the number of goblet cells in the small intestine in the AFB(1) group significantly decreased. Also, AFB(1) evidently decreased the mRNA expression of TLR2-2, TLR4, and TLR7 in the small intestine. Taken together, our study indicated that dietary 0.6 mg/kg AFB(1) could induce histopathological injuries and ultrastructural changes, and depress levels of TLR mRNA in the chicken small intestine. MDPI 2018-03-21 /pmc/articles/PMC5923297/ /pubmed/29561786 http://dx.doi.org/10.3390/toxins10040131 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Fengyuan
Zuo, Zhicai
Chen, Kejie
Gao, Caixia
Yang, Zhuangzhi
Zhao, Song
Li, Jianzhen
Song, Hetao
Peng, Xi
Fang, Jing
Cui, Hengmin
Ouyang, Ping
Zhou, Yi
Shu, Gang
Jing, Bo
Histopathological Injuries, Ultrastructural Changes, and Depressed TLR Expression in the Small Intestine of Broiler Chickens with Aflatoxin B(1)
title Histopathological Injuries, Ultrastructural Changes, and Depressed TLR Expression in the Small Intestine of Broiler Chickens with Aflatoxin B(1)
title_full Histopathological Injuries, Ultrastructural Changes, and Depressed TLR Expression in the Small Intestine of Broiler Chickens with Aflatoxin B(1)
title_fullStr Histopathological Injuries, Ultrastructural Changes, and Depressed TLR Expression in the Small Intestine of Broiler Chickens with Aflatoxin B(1)
title_full_unstemmed Histopathological Injuries, Ultrastructural Changes, and Depressed TLR Expression in the Small Intestine of Broiler Chickens with Aflatoxin B(1)
title_short Histopathological Injuries, Ultrastructural Changes, and Depressed TLR Expression in the Small Intestine of Broiler Chickens with Aflatoxin B(1)
title_sort histopathological injuries, ultrastructural changes, and depressed tlr expression in the small intestine of broiler chickens with aflatoxin b(1)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923297/
https://www.ncbi.nlm.nih.gov/pubmed/29561786
http://dx.doi.org/10.3390/toxins10040131
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