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A new therapy against ulcerative colitis via the intestine and brain using the Si-based agent
Ulcerative colitis (UC) is a non-specific inflammatory bowel disease that causes ulcers and erosions in the colonic mucosa and becomes chronic with cycles of amelioration and exacerbation. Because its exact etiology remains largely unclear, and the primary therapy is limited to symptomatic treatment...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187638/ https://www.ncbi.nlm.nih.gov/pubmed/35688905 http://dx.doi.org/10.1038/s41598-022-13655-7 |
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author | Koyama, Yoshihisa Kobayashi, Yuki Hirota, Ikuei Sun, Yuanjie Ohtsu, Iwao Imai, Hiroe Yoshioka, Yoshichika Yanagawa, Hiroto Sumi, Takuya Kobayashi, Hikaru Shimada, Shoichi |
author_facet | Koyama, Yoshihisa Kobayashi, Yuki Hirota, Ikuei Sun, Yuanjie Ohtsu, Iwao Imai, Hiroe Yoshioka, Yoshichika Yanagawa, Hiroto Sumi, Takuya Kobayashi, Hikaru Shimada, Shoichi |
author_sort | Koyama, Yoshihisa |
collection | PubMed |
description | Ulcerative colitis (UC) is a non-specific inflammatory bowel disease that causes ulcers and erosions in the colonic mucosa and becomes chronic with cycles of amelioration and exacerbation. Because its exact etiology remains largely unclear, and the primary therapy is limited to symptomatic treatment, the development of new therapeutic agent for UC is highly desired. Because one of the disease pathogenesis is involvement of oxidative stress, it is likely that an appropriate antioxidant will be an effective therapeutic agent for UC. Our silicon (Si)-based agent, when ingested, allowed for stable and persistent generation of massive amounts of hydrogen in the gastrointestinal tract. We demonstrated the Si-based agent alleviated the mental symptom as well as the gastrointestinal symptoms, inflammation, and oxidation associated with dextran sodium sulfate-induced UC model through Hydrogen and antioxidant sulfur compounds. As the Si-based agent was effective in treating UC in the brain and large intestine of mice, it was considered to be capable of suppressing exacerbations and sustaining remission of UC. |
format | Online Article Text |
id | pubmed-9187638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91876382022-06-12 A new therapy against ulcerative colitis via the intestine and brain using the Si-based agent Koyama, Yoshihisa Kobayashi, Yuki Hirota, Ikuei Sun, Yuanjie Ohtsu, Iwao Imai, Hiroe Yoshioka, Yoshichika Yanagawa, Hiroto Sumi, Takuya Kobayashi, Hikaru Shimada, Shoichi Sci Rep Article Ulcerative colitis (UC) is a non-specific inflammatory bowel disease that causes ulcers and erosions in the colonic mucosa and becomes chronic with cycles of amelioration and exacerbation. Because its exact etiology remains largely unclear, and the primary therapy is limited to symptomatic treatment, the development of new therapeutic agent for UC is highly desired. Because one of the disease pathogenesis is involvement of oxidative stress, it is likely that an appropriate antioxidant will be an effective therapeutic agent for UC. Our silicon (Si)-based agent, when ingested, allowed for stable and persistent generation of massive amounts of hydrogen in the gastrointestinal tract. We demonstrated the Si-based agent alleviated the mental symptom as well as the gastrointestinal symptoms, inflammation, and oxidation associated with dextran sodium sulfate-induced UC model through Hydrogen and antioxidant sulfur compounds. As the Si-based agent was effective in treating UC in the brain and large intestine of mice, it was considered to be capable of suppressing exacerbations and sustaining remission of UC. Nature Publishing Group UK 2022-06-10 /pmc/articles/PMC9187638/ /pubmed/35688905 http://dx.doi.org/10.1038/s41598-022-13655-7 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Koyama, Yoshihisa Kobayashi, Yuki Hirota, Ikuei Sun, Yuanjie Ohtsu, Iwao Imai, Hiroe Yoshioka, Yoshichika Yanagawa, Hiroto Sumi, Takuya Kobayashi, Hikaru Shimada, Shoichi A new therapy against ulcerative colitis via the intestine and brain using the Si-based agent |
title | A new therapy against ulcerative colitis via the intestine and brain using the Si-based agent |
title_full | A new therapy against ulcerative colitis via the intestine and brain using the Si-based agent |
title_fullStr | A new therapy against ulcerative colitis via the intestine and brain using the Si-based agent |
title_full_unstemmed | A new therapy against ulcerative colitis via the intestine and brain using the Si-based agent |
title_short | A new therapy against ulcerative colitis via the intestine and brain using the Si-based agent |
title_sort | new therapy against ulcerative colitis via the intestine and brain using the si-based agent |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187638/ https://www.ncbi.nlm.nih.gov/pubmed/35688905 http://dx.doi.org/10.1038/s41598-022-13655-7 |
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