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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...

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Autores principales: Morikawa, Takanori, Shimasaki, Miyako, Ichiseki, Toru, Ueda, Shusuke, Ueda, Yoshimichi, Takahashi, Kan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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