このエントリーをはてなブックマークに追加


ID 67676
FullText URL
fulltext.pdf 1.73 MB
Author
Hayashida, Tomohiro Department of Cardiovascular Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kuroko, Yosuke Department of Cardiovascular Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences and Okayama University Hospital
Shimizu, Shuji Department of Cardiovascular Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Akiyama, Tsuyoshi Department of Cardiac Physiology, National Cerebral and Cardiovascular Center
Suezawa, Takanori Department of Cardiovascular Surgery, Fukuyama City Hospital
Kioka, Yukio Department of Cardiovascular Surgery, Fukuyama City Hospital
Kotani, Yasuhiro Department of Cardiovascular Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences and Okayama University Hospital
Shishido, Toshiaki Department of Research Promotion and Management, National Cerebral and Cardiovascular Center
Kasahara, Shingo Department of Cardiovascular Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences and Okayama University Hospital Kaken ID publons
Abstract
It has been suggested that sodium-glucose cotransporter 2 (SGLT2) inhibitors have cardioprotective effects during myocardial ischemia/reperfusion (I/R) independent of glucose-lowering action. However, the effects of SGLT2 inhibitors on structural damage to cardiomyocytes in the ischemic region during I/R remain unknown. We applied a microdialysis technique to the heart of anesthetized rats and investigated the effects of an SGLT2 inhibitor, dapagliflozin, on myocardial interstitial myoglobin levels in the ischemic region during coronary occlusion followed by reperfusion. Dapagliflozin was administered systemically (40 mu g/body iv) or locally via a dialysis probe (100 mu M and 1 mM) 30 min before coronary occlusion. In the vehicle group, coronary occlusion increased the dialysate myoglobin concentration in the ischemic region. Reperfusion further increased the dialysate myoglobin concentration. Intravenous administration of dapagliflozin reduced dialysate myoglobin concentration during ischemia and at 0-15 min after reperfusion, but local administration (100 mu M and 1 mM) did not. Therefore, acute systemic administration of dapagliflozin prior to ischemia has cardioprotective effects on structural damage during I/R.
Keywords
Sodium-glucose-cotransporter 2 inhibitor
Dapagliflozin
Myocardial ischemia/reperfusion
Cardiac microdialysis
Myoglobin
Note
The version of record of this article, first published in Scientific Reports, is available online at Publisher’s website: http://dx.doi.org/10.1038/s41598-024-67195-3
Published Date
2024-07-16
Publication Title
Scientific Reports
Volume
volume14
Issue
issue1
Publisher
Nature Portfolio
Start Page
16337
ISSN
2045-2322
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© The Author(s) 2024
File Version
publisher
PubMed ID
DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.1038/s41598-024-67195-3
License
http://creativecommons.org/licenses/by/4.0/
Citation
Hayashida, T., Kuroko, Y., Shimizu, S. et al. Effects of dapagliflozin on myoglobin efflux from cardiomyocyte during myocardial ischemia/reperfusion in anesthetized rats. Sci Rep 14, 16337 (2024). https://doi.org/10.1038/s41598-024-67195-3
Funder Name
Japan Society for the Promotion of Science
助成番号
JP19K09417
JP22K09182