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A novel soluble epoxide hydrolase vaccine protects murine cardiac muscle against myocardial infarction
Myocardial infarction is still a life-threatening disease, even though its prognosis has been improved through the development of percutaneous coronary intervention and pharmacotherapy. In addition, heart failure due to remodeling after myocardial infarction requires lifelong management. The aim of...
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/PMC9051153/ https://www.ncbi.nlm.nih.gov/pubmed/35484372 http://dx.doi.org/10.1038/s41598-022-10641-x |
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author | Kitsuka, Takahiro Shiraki, Aya Oyama, Jun-ichi Nakagami, Hironori Tanaka, Atsushi Node, Koichi |
author_facet | Kitsuka, Takahiro Shiraki, Aya Oyama, Jun-ichi Nakagami, Hironori Tanaka, Atsushi Node, Koichi |
author_sort | Kitsuka, Takahiro |
collection | PubMed |
description | Myocardial infarction is still a life-threatening disease, even though its prognosis has been improved through the development of percutaneous coronary intervention and pharmacotherapy. In addition, heart failure due to remodeling after myocardial infarction requires lifelong management. The aim of this study was to develop a novel treatment suppressing the myocardial damage done by myocardial infarction. We focused on inhibition of soluble epoxide hydrolase to prolong the activation of epoxyeicosatrienoic acids, which have vasodilatory and anti-inflammatory properties. We successfully made a new vaccine to inactivate soluble epoxide hydrolase, and we have evaluated the effect of the vaccine in a rat myocardial infarction model. In the vaccinated group, the ischemic area was significantly reduced, and cardiac function was significantly preserved. Vaccine treatment clearly increased microvessels in the border area and suppressed fibrosis secondary to myocardial infarction. This soluble epoxide hydrolase vaccine is a novel treatment for improving cardiac function following myocardial infarction. |
format | Online Article Text |
id | pubmed-9051153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90511532022-04-30 A novel soluble epoxide hydrolase vaccine protects murine cardiac muscle against myocardial infarction Kitsuka, Takahiro Shiraki, Aya Oyama, Jun-ichi Nakagami, Hironori Tanaka, Atsushi Node, Koichi Sci Rep Article Myocardial infarction is still a life-threatening disease, even though its prognosis has been improved through the development of percutaneous coronary intervention and pharmacotherapy. In addition, heart failure due to remodeling after myocardial infarction requires lifelong management. The aim of this study was to develop a novel treatment suppressing the myocardial damage done by myocardial infarction. We focused on inhibition of soluble epoxide hydrolase to prolong the activation of epoxyeicosatrienoic acids, which have vasodilatory and anti-inflammatory properties. We successfully made a new vaccine to inactivate soluble epoxide hydrolase, and we have evaluated the effect of the vaccine in a rat myocardial infarction model. In the vaccinated group, the ischemic area was significantly reduced, and cardiac function was significantly preserved. Vaccine treatment clearly increased microvessels in the border area and suppressed fibrosis secondary to myocardial infarction. This soluble epoxide hydrolase vaccine is a novel treatment for improving cardiac function following myocardial infarction. Nature Publishing Group UK 2022-04-28 /pmc/articles/PMC9051153/ /pubmed/35484372 http://dx.doi.org/10.1038/s41598-022-10641-x 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 Kitsuka, Takahiro Shiraki, Aya Oyama, Jun-ichi Nakagami, Hironori Tanaka, Atsushi Node, Koichi A novel soluble epoxide hydrolase vaccine protects murine cardiac muscle against myocardial infarction |
title | A novel soluble epoxide hydrolase vaccine protects murine cardiac muscle against myocardial infarction |
title_full | A novel soluble epoxide hydrolase vaccine protects murine cardiac muscle against myocardial infarction |
title_fullStr | A novel soluble epoxide hydrolase vaccine protects murine cardiac muscle against myocardial infarction |
title_full_unstemmed | A novel soluble epoxide hydrolase vaccine protects murine cardiac muscle against myocardial infarction |
title_short | A novel soluble epoxide hydrolase vaccine protects murine cardiac muscle against myocardial infarction |
title_sort | novel soluble epoxide hydrolase vaccine protects murine cardiac muscle against myocardial infarction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051153/ https://www.ncbi.nlm.nih.gov/pubmed/35484372 http://dx.doi.org/10.1038/s41598-022-10641-x |
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