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Oxazolone-induced gastrointestinal disorders enhance the oral transmission of AA amyloidosis in mice

Amyloid A (AA) amyloidosis is a lethal disease characterized by systemic AA amyloid deposition, and is reported in many animal species. Despite experiments have shown that AA amyloidosis can be transmitted orally, horizontal transmission and cross-species transmission are concerns, the transmission...

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Autores principales: KOBAYASHI, Hiroto, IWAIDE, Susumu, UJIKE, Naoki, MURAKAMI, Tomoaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267199/
https://www.ncbi.nlm.nih.gov/pubmed/33883362
http://dx.doi.org/10.1292/jvms.21-0022
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author KOBAYASHI, Hiroto
IWAIDE, Susumu
UJIKE, Naoki
MURAKAMI, Tomoaki
author_facet KOBAYASHI, Hiroto
IWAIDE, Susumu
UJIKE, Naoki
MURAKAMI, Tomoaki
author_sort KOBAYASHI, Hiroto
collection PubMed
description Amyloid A (AA) amyloidosis is a lethal disease characterized by systemic AA amyloid deposition, and is reported in many animal species. Despite experiments have shown that AA amyloidosis can be transmitted orally, horizontal transmission and cross-species transmission are concerns, the transmission mechanism has been unknown. In this study, we examined the oral transmission efficiency of AA amyloidosis using oxazolone-induced gastrointestinal disorder mice. As a result, the upper or lower gastrointestinal disorder groups developed more severe amyloid deposition in systemic tissues than the group without gastrointestinal disorders. The results of this study suggest that gastrointestinal damage promotes the oral transmission of AA amyloidosis.
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spelling pubmed-82671992021-07-14 Oxazolone-induced gastrointestinal disorders enhance the oral transmission of AA amyloidosis in mice KOBAYASHI, Hiroto IWAIDE, Susumu UJIKE, Naoki MURAKAMI, Tomoaki J Vet Med Sci Pathology Amyloid A (AA) amyloidosis is a lethal disease characterized by systemic AA amyloid deposition, and is reported in many animal species. Despite experiments have shown that AA amyloidosis can be transmitted orally, horizontal transmission and cross-species transmission are concerns, the transmission mechanism has been unknown. In this study, we examined the oral transmission efficiency of AA amyloidosis using oxazolone-induced gastrointestinal disorder mice. As a result, the upper or lower gastrointestinal disorder groups developed more severe amyloid deposition in systemic tissues than the group without gastrointestinal disorders. The results of this study suggest that gastrointestinal damage promotes the oral transmission of AA amyloidosis. The Japanese Society of Veterinary Science 2021-04-20 2021-06 /pmc/articles/PMC8267199/ /pubmed/33883362 http://dx.doi.org/10.1292/jvms.21-0022 Text en ©2021 The Japanese Society of Veterinary Science https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Pathology
KOBAYASHI, Hiroto
IWAIDE, Susumu
UJIKE, Naoki
MURAKAMI, Tomoaki
Oxazolone-induced gastrointestinal disorders enhance the oral transmission of AA amyloidosis in mice
title Oxazolone-induced gastrointestinal disorders enhance the oral transmission of AA amyloidosis in mice
title_full Oxazolone-induced gastrointestinal disorders enhance the oral transmission of AA amyloidosis in mice
title_fullStr Oxazolone-induced gastrointestinal disorders enhance the oral transmission of AA amyloidosis in mice
title_full_unstemmed Oxazolone-induced gastrointestinal disorders enhance the oral transmission of AA amyloidosis in mice
title_short Oxazolone-induced gastrointestinal disorders enhance the oral transmission of AA amyloidosis in mice
title_sort oxazolone-induced gastrointestinal disorders enhance the oral transmission of aa amyloidosis in mice
topic Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267199/
https://www.ncbi.nlm.nih.gov/pubmed/33883362
http://dx.doi.org/10.1292/jvms.21-0022
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