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Fox smell abrogates the effect of herbal odor to prolong mouse cardiac allograft survival
BACKGROUND: Herbal medicines have unique odors, and the act of smelling may have modulatory effects on the immune system. We investigated the effect of olfactory exposure to Tokishakuyaku-san (TJ-23), a Japanese herbal medicine, on alloimmune responses in a murine model of cardiac allograft transpla...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026832/ https://www.ncbi.nlm.nih.gov/pubmed/24886081 http://dx.doi.org/10.1186/1749-8090-9-82 |
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author | Jin, Xiangyuan Uchiyama, Masateru Zhang, Qi Niimi, Masanori |
author_facet | Jin, Xiangyuan Uchiyama, Masateru Zhang, Qi Niimi, Masanori |
author_sort | Jin, Xiangyuan |
collection | PubMed |
description | BACKGROUND: Herbal medicines have unique odors, and the act of smelling may have modulatory effects on the immune system. We investigated the effect of olfactory exposure to Tokishakuyaku-san (TJ-23), a Japanese herbal medicine, on alloimmune responses in a murine model of cardiac allograft transplantation. METHODS: Naïve or olfactory-dysfunctional CBA mice underwent transplantation of a C57BL/6 heart and were exposed to the odor of TJ-23 until rejection. Some naïve CBA recipients of an allograft were given olfactory exposure to Sairei-to (TJ-114), trimethylthiazoline (TMT), individual components of TJ-23, or a TJ-23 preparation lacking one component. Adoptive transfer studies were performed to determine whether regulatory cells were generated. RESULTS: Untreated CBA mice rejected their C57BL/6 allografts acutely, as did olfactory-dysfunctional CBA mice exposed to the odor of TJ-23. CBA recipients of a C57BL/6 heart given olfactory exposure to TJ-23 had significantly prolonged allograft survival, whereas those exposed to the odor of TJ-114, TMT, one component of TJ-23, or TJ-23 lacking a component did not. Secondary allograft recipients that were given, at 30 days after transplantation, either whole splenocytes, CD4(+) cells, or CD4(+)CD25(+) cells from primary recipients exposed to the odor of TJ-23 had indefinitely prolonged allograft survival. CONCLUSIONS: Prolonged survival of cardiac allografts and generation of regulatory cells was associated with exposure to the odor of TJ-23 in our model. The olfactory area of the brain may have a role in the modulation of immune responses. |
format | Online Article Text |
id | pubmed-4026832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40268322014-05-21 Fox smell abrogates the effect of herbal odor to prolong mouse cardiac allograft survival Jin, Xiangyuan Uchiyama, Masateru Zhang, Qi Niimi, Masanori J Cardiothorac Surg Research Article BACKGROUND: Herbal medicines have unique odors, and the act of smelling may have modulatory effects on the immune system. We investigated the effect of olfactory exposure to Tokishakuyaku-san (TJ-23), a Japanese herbal medicine, on alloimmune responses in a murine model of cardiac allograft transplantation. METHODS: Naïve or olfactory-dysfunctional CBA mice underwent transplantation of a C57BL/6 heart and were exposed to the odor of TJ-23 until rejection. Some naïve CBA recipients of an allograft were given olfactory exposure to Sairei-to (TJ-114), trimethylthiazoline (TMT), individual components of TJ-23, or a TJ-23 preparation lacking one component. Adoptive transfer studies were performed to determine whether regulatory cells were generated. RESULTS: Untreated CBA mice rejected their C57BL/6 allografts acutely, as did olfactory-dysfunctional CBA mice exposed to the odor of TJ-23. CBA recipients of a C57BL/6 heart given olfactory exposure to TJ-23 had significantly prolonged allograft survival, whereas those exposed to the odor of TJ-114, TMT, one component of TJ-23, or TJ-23 lacking a component did not. Secondary allograft recipients that were given, at 30 days after transplantation, either whole splenocytes, CD4(+) cells, or CD4(+)CD25(+) cells from primary recipients exposed to the odor of TJ-23 had indefinitely prolonged allograft survival. CONCLUSIONS: Prolonged survival of cardiac allografts and generation of regulatory cells was associated with exposure to the odor of TJ-23 in our model. The olfactory area of the brain may have a role in the modulation of immune responses. BioMed Central 2014-05-09 /pmc/articles/PMC4026832/ /pubmed/24886081 http://dx.doi.org/10.1186/1749-8090-9-82 Text en Copyright © 2014 Jin 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 credited. 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. |
spellingShingle | Research Article Jin, Xiangyuan Uchiyama, Masateru Zhang, Qi Niimi, Masanori Fox smell abrogates the effect of herbal odor to prolong mouse cardiac allograft survival |
title | Fox smell abrogates the effect of herbal odor to prolong mouse cardiac allograft survival |
title_full | Fox smell abrogates the effect of herbal odor to prolong mouse cardiac allograft survival |
title_fullStr | Fox smell abrogates the effect of herbal odor to prolong mouse cardiac allograft survival |
title_full_unstemmed | Fox smell abrogates the effect of herbal odor to prolong mouse cardiac allograft survival |
title_short | Fox smell abrogates the effect of herbal odor to prolong mouse cardiac allograft survival |
title_sort | fox smell abrogates the effect of herbal odor to prolong mouse cardiac allograft survival |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026832/ https://www.ncbi.nlm.nih.gov/pubmed/24886081 http://dx.doi.org/10.1186/1749-8090-9-82 |
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