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The Possibility of IPC to Prevent Ischemic-Reperfusion Injury in Skeletal Muscle in a Rat
Blood removal with air tourniquets for a long time induces muscle damage after reperfusion. Ischemic preconditioning (IPC) has a protective effect against ischemia-reperfusion injury in striated muscle and myocardium. However, the mechanism of action of IPC on skeletal muscle injury is unclear. Thus...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964745/ https://www.ncbi.nlm.nih.gov/pubmed/36836038 http://dx.doi.org/10.3390/jcm12041501 |
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author | Morikawa, Takanori Shimasaki, Miyako Ichiseki, Toru Ueda, Shusuke Ueda, Yoshimichi Takahashi, Kan |
author_facet | Morikawa, Takanori Shimasaki, Miyako Ichiseki, Toru Ueda, Shusuke Ueda, Yoshimichi Takahashi, Kan |
author_sort | Morikawa, Takanori |
collection | PubMed |
description | Blood removal with air tourniquets for a long time induces muscle damage after reperfusion. Ischemic preconditioning (IPC) has a protective effect against ischemia-reperfusion injury in striated muscle and myocardium. However, the mechanism of action of IPC on skeletal muscle injury is unclear. Thus, this study aimed to investigate the effect of IPC in reducing skeletal muscle damage caused by ischemia-reperfusion injury. The hindlimbs of 6-month-old rats were wounded with air tourniquets at a carminative blood pressure of 300 mmHg on the thighs. Rats were divided into the IPC (−) group and the IPC (+) group. The vascular endothelial growth factor (VEGF), 8-hydroxyguanosine (8-OHdG), and cyclooxygenase 2 (COX-2) were investigated by protein levels. Quantitative analysis of apoptosis was performed using the TUNEL method. Compared with the IPC (−) group, the IPC (+) group retained the VEGF expression, and the COX-2 and 8-OHdG expressions were suppressed. The proportion of apoptosis cells decreased in the IPC (+) group compared with the IPC (−) group. IPC in skeletal muscles proliferated VEGF and suppressed inflammatory response and oxidative DNA damage. IPC has the potential to reduce muscle damage after ischemia-reperfusion. |
format | Online Article Text |
id | pubmed-9964745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99647452023-02-26 The Possibility of IPC to Prevent Ischemic-Reperfusion Injury in Skeletal Muscle in a Rat Morikawa, Takanori Shimasaki, Miyako Ichiseki, Toru Ueda, Shusuke Ueda, Yoshimichi Takahashi, Kan J Clin Med Article Blood removal with air tourniquets for a long time induces muscle damage after reperfusion. Ischemic preconditioning (IPC) has a protective effect against ischemia-reperfusion injury in striated muscle and myocardium. However, the mechanism of action of IPC on skeletal muscle injury is unclear. Thus, this study aimed to investigate the effect of IPC in reducing skeletal muscle damage caused by ischemia-reperfusion injury. The hindlimbs of 6-month-old rats were wounded with air tourniquets at a carminative blood pressure of 300 mmHg on the thighs. Rats were divided into the IPC (−) group and the IPC (+) group. The vascular endothelial growth factor (VEGF), 8-hydroxyguanosine (8-OHdG), and cyclooxygenase 2 (COX-2) were investigated by protein levels. Quantitative analysis of apoptosis was performed using the TUNEL method. Compared with the IPC (−) group, the IPC (+) group retained the VEGF expression, and the COX-2 and 8-OHdG expressions were suppressed. The proportion of apoptosis cells decreased in the IPC (+) group compared with the IPC (−) group. IPC in skeletal muscles proliferated VEGF and suppressed inflammatory response and oxidative DNA damage. IPC has the potential to reduce muscle damage after ischemia-reperfusion. MDPI 2023-02-14 /pmc/articles/PMC9964745/ /pubmed/36836038 http://dx.doi.org/10.3390/jcm12041501 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Morikawa, Takanori Shimasaki, Miyako Ichiseki, Toru Ueda, Shusuke Ueda, Yoshimichi Takahashi, Kan The Possibility of IPC to Prevent Ischemic-Reperfusion Injury in Skeletal Muscle in a Rat |
title | The Possibility of IPC to Prevent Ischemic-Reperfusion Injury in Skeletal Muscle in a Rat |
title_full | The Possibility of IPC to Prevent Ischemic-Reperfusion Injury in Skeletal Muscle in a Rat |
title_fullStr | The Possibility of IPC to Prevent Ischemic-Reperfusion Injury in Skeletal Muscle in a Rat |
title_full_unstemmed | The Possibility of IPC to Prevent Ischemic-Reperfusion Injury in Skeletal Muscle in a Rat |
title_short | The Possibility of IPC to Prevent Ischemic-Reperfusion Injury in Skeletal Muscle in a Rat |
title_sort | possibility of ipc to prevent ischemic-reperfusion injury in skeletal muscle in a rat |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964745/ https://www.ncbi.nlm.nih.gov/pubmed/36836038 http://dx.doi.org/10.3390/jcm12041501 |
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