Acute dapagliflozin administration exerts cardioprotective effects in rats with cardiac ischemia/reperfusion injury

© 2020 The Author(s). Background: A sodium-glucose co-transporter 2 (SGLT-2) inhibitor had favorable impact on the attenuation of hyperglycemia together with the severity of heart failure. However, the effects of acute dapagliflozin administration at the time of cardiac ischemia/reperfusion (I/R) in...

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Main Authors: Sarayut Lahnwong, Siripong Palee, Nattayaporn Apaijai, Sirawit Sriwichaiin, Sasiwan Kerdphoo, Thidarat Jaiwongkam, Siriporn C. Chattipakorn, Nipon Chattipakorn
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Published: 2020
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/70835
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spelling th-cmuir.6653943832-708352020-10-14T08:42:10Z Acute dapagliflozin administration exerts cardioprotective effects in rats with cardiac ischemia/reperfusion injury Sarayut Lahnwong Siripong Palee Nattayaporn Apaijai Sirawit Sriwichaiin Sasiwan Kerdphoo Thidarat Jaiwongkam Siriporn C. Chattipakorn Nipon Chattipakorn Medicine © 2020 The Author(s). Background: A sodium-glucose co-transporter 2 (SGLT-2) inhibitor had favorable impact on the attenuation of hyperglycemia together with the severity of heart failure. However, the effects of acute dapagliflozin administration at the time of cardiac ischemia/reperfusion (I/R) injury are not established. Methods: The effects of dapagliflozin on cardiac function were investigated by treating cardiac I/R injury at different time points. Cardiac I/R was instigated in forty-eight Wistar rats. These rats were then split into 4 interventional groups: control, dapagliflozin (SGLT2 inhibitor, 1 mg/kg) given pre-ischemia, at the time of ischemia and at the beginning of reperfusion. Left ventricular (LV) function and arrhythmia score were evaluated. The hearts were used to evaluate size of myocardial infarction, cardiomyocyte apoptosis, cardiac mitochondrial dynamics and function. Results: Dapagliflozin given pre-ischemia conferred the maximum level of cardioprotection quantified through the decrease in arrhythmia, attenuated infarct size, decreased cardiac apoptosis and improved cardiac mitochondrial function, biogenesis and dynamics, leading to LV function improvement during cardiac I/R injury. Dapagliflozin given during ischemia also showed cardioprotection, but at a lower level of efficacy. Conclusions: Acute dapagliflozin administration during cardiac I/R injury exerted cardioprotective effects by attenuating cardiac infarct size, increasing LV function and reducing arrhythmias. These benefits indicate its potential clinical usefulness. 2020-10-14T08:42:10Z 2020-10-14T08:42:10Z 2020-06-15 Journal 14752840 2-s2.0-85086620246 10.1186/s12933-020-01066-9 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85086620246&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/70835
institution Chiang Mai University
building Chiang Mai University Library
continent Asia
country Thailand
Thailand
content_provider Chiang Mai University Library
collection CMU Intellectual Repository
topic Medicine
spellingShingle Medicine
Sarayut Lahnwong
Siripong Palee
Nattayaporn Apaijai
Sirawit Sriwichaiin
Sasiwan Kerdphoo
Thidarat Jaiwongkam
Siriporn C. Chattipakorn
Nipon Chattipakorn
Acute dapagliflozin administration exerts cardioprotective effects in rats with cardiac ischemia/reperfusion injury
description © 2020 The Author(s). Background: A sodium-glucose co-transporter 2 (SGLT-2) inhibitor had favorable impact on the attenuation of hyperglycemia together with the severity of heart failure. However, the effects of acute dapagliflozin administration at the time of cardiac ischemia/reperfusion (I/R) injury are not established. Methods: The effects of dapagliflozin on cardiac function were investigated by treating cardiac I/R injury at different time points. Cardiac I/R was instigated in forty-eight Wistar rats. These rats were then split into 4 interventional groups: control, dapagliflozin (SGLT2 inhibitor, 1 mg/kg) given pre-ischemia, at the time of ischemia and at the beginning of reperfusion. Left ventricular (LV) function and arrhythmia score were evaluated. The hearts were used to evaluate size of myocardial infarction, cardiomyocyte apoptosis, cardiac mitochondrial dynamics and function. Results: Dapagliflozin given pre-ischemia conferred the maximum level of cardioprotection quantified through the decrease in arrhythmia, attenuated infarct size, decreased cardiac apoptosis and improved cardiac mitochondrial function, biogenesis and dynamics, leading to LV function improvement during cardiac I/R injury. Dapagliflozin given during ischemia also showed cardioprotection, but at a lower level of efficacy. Conclusions: Acute dapagliflozin administration during cardiac I/R injury exerted cardioprotective effects by attenuating cardiac infarct size, increasing LV function and reducing arrhythmias. These benefits indicate its potential clinical usefulness.
format Journal
author Sarayut Lahnwong
Siripong Palee
Nattayaporn Apaijai
Sirawit Sriwichaiin
Sasiwan Kerdphoo
Thidarat Jaiwongkam
Siriporn C. Chattipakorn
Nipon Chattipakorn
author_facet Sarayut Lahnwong
Siripong Palee
Nattayaporn Apaijai
Sirawit Sriwichaiin
Sasiwan Kerdphoo
Thidarat Jaiwongkam
Siriporn C. Chattipakorn
Nipon Chattipakorn
author_sort Sarayut Lahnwong
title Acute dapagliflozin administration exerts cardioprotective effects in rats with cardiac ischemia/reperfusion injury
title_short Acute dapagliflozin administration exerts cardioprotective effects in rats with cardiac ischemia/reperfusion injury
title_full Acute dapagliflozin administration exerts cardioprotective effects in rats with cardiac ischemia/reperfusion injury
title_fullStr Acute dapagliflozin administration exerts cardioprotective effects in rats with cardiac ischemia/reperfusion injury
title_full_unstemmed Acute dapagliflozin administration exerts cardioprotective effects in rats with cardiac ischemia/reperfusion injury
title_sort acute dapagliflozin administration exerts cardioprotective effects in rats with cardiac ischemia/reperfusion injury
publishDate 2020
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85086620246&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/70835
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