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Protective effects of gallic acid on cardiac electrophysiology and arrhythmias during reperfusion in diabetes

OBJECTIVE(S): Gallic acid (GA), a potent anti-oxidant, plays an important role in reducing diabetic induced cardiac disorders. Therefore, the present investigation was purposed to determine the beneficial effect of GA in cardiac arrhythmias during reperfusion in diabetes induced by alloxan. MATERIAL...

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Autores principales: Ramezani-Aliakbari, Fatemeh, Badavi, Mohammad, Dianat, Mahin, Mard, Seyed Ali, Ahangarpour, Akram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556507/
https://www.ncbi.nlm.nih.gov/pubmed/31217931
http://dx.doi.org/10.22038/ijbms.2019.27563.6726
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author Ramezani-Aliakbari, Fatemeh
Badavi, Mohammad
Dianat, Mahin
Mard, Seyed Ali
Ahangarpour, Akram
author_facet Ramezani-Aliakbari, Fatemeh
Badavi, Mohammad
Dianat, Mahin
Mard, Seyed Ali
Ahangarpour, Akram
author_sort Ramezani-Aliakbari, Fatemeh
collection PubMed
description OBJECTIVE(S): Gallic acid (GA), a potent anti-oxidant, plays an important role in reducing diabetic induced cardiac disorders. Therefore, the present investigation was purposed to determine the beneficial effect of GA in cardiac arrhythmias during reperfusion in diabetes induced by alloxan. MATERIALS AND METHODS: Male Sprague-Dawley rats (200–250 g) were randomly divided into three groups (eight in each group): control (C), diabetic (D), and diabetic treated with GA (D+G) groups. GA was administered by gavage (25 mg/kg, daily) for eight weeks. Diabetes was induced by a single intraperitoneal injection of alloxan (120 mg/kg). Ischemia-reperfusion (IR) injury was performed by ischemia and then reperfusion (30 and 120 min, respectively). The score and magnitude of arrhythmias, creatine kinase (CK-MB), and lactate dehydrogenase (LDH) of the heart, electrocardiographic, and hemodynamic parameters were measured. One-way ANOVA followed by LSD tests were used for the differences between groups. The percentage of incidence was also evaluated by Fisher’s exact test. RESULTS: The duration (P<0.05), onset (P<0.01), score and incidence of arrhythmia, QT interval (P<0.001), LDH, and CK-MB (P<0.05) were significantly elevated and the contractility of the heart (±dp/dt, P<0.01), LVSP, QRS complex voltage (P<0.05), and heart rate (P<0.01) were significantly reduced in the diabetic animals compared with the control rats. However, administration with GA significantly improved these alterations in the diabetic group compared with the diabetic animals. CONCLUSION: This study indicated the beneficial effects of GA on cardiac electrophysiology and arrhythmias during reperfusion in diabetes.
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spelling pubmed-65565072019-06-19 Protective effects of gallic acid on cardiac electrophysiology and arrhythmias during reperfusion in diabetes Ramezani-Aliakbari, Fatemeh Badavi, Mohammad Dianat, Mahin Mard, Seyed Ali Ahangarpour, Akram Iran J Basic Med Sci Original Article OBJECTIVE(S): Gallic acid (GA), a potent anti-oxidant, plays an important role in reducing diabetic induced cardiac disorders. Therefore, the present investigation was purposed to determine the beneficial effect of GA in cardiac arrhythmias during reperfusion in diabetes induced by alloxan. MATERIALS AND METHODS: Male Sprague-Dawley rats (200–250 g) were randomly divided into three groups (eight in each group): control (C), diabetic (D), and diabetic treated with GA (D+G) groups. GA was administered by gavage (25 mg/kg, daily) for eight weeks. Diabetes was induced by a single intraperitoneal injection of alloxan (120 mg/kg). Ischemia-reperfusion (IR) injury was performed by ischemia and then reperfusion (30 and 120 min, respectively). The score and magnitude of arrhythmias, creatine kinase (CK-MB), and lactate dehydrogenase (LDH) of the heart, electrocardiographic, and hemodynamic parameters were measured. One-way ANOVA followed by LSD tests were used for the differences between groups. The percentage of incidence was also evaluated by Fisher’s exact test. RESULTS: The duration (P<0.05), onset (P<0.01), score and incidence of arrhythmia, QT interval (P<0.001), LDH, and CK-MB (P<0.05) were significantly elevated and the contractility of the heart (±dp/dt, P<0.01), LVSP, QRS complex voltage (P<0.05), and heart rate (P<0.01) were significantly reduced in the diabetic animals compared with the control rats. However, administration with GA significantly improved these alterations in the diabetic group compared with the diabetic animals. CONCLUSION: This study indicated the beneficial effects of GA on cardiac electrophysiology and arrhythmias during reperfusion in diabetes. Mashhad University of Medical Sciences 2019-05 /pmc/articles/PMC6556507/ /pubmed/31217931 http://dx.doi.org/10.22038/ijbms.2019.27563.6726 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ramezani-Aliakbari, Fatemeh
Badavi, Mohammad
Dianat, Mahin
Mard, Seyed Ali
Ahangarpour, Akram
Protective effects of gallic acid on cardiac electrophysiology and arrhythmias during reperfusion in diabetes
title Protective effects of gallic acid on cardiac electrophysiology and arrhythmias during reperfusion in diabetes
title_full Protective effects of gallic acid on cardiac electrophysiology and arrhythmias during reperfusion in diabetes
title_fullStr Protective effects of gallic acid on cardiac electrophysiology and arrhythmias during reperfusion in diabetes
title_full_unstemmed Protective effects of gallic acid on cardiac electrophysiology and arrhythmias during reperfusion in diabetes
title_short Protective effects of gallic acid on cardiac electrophysiology and arrhythmias during reperfusion in diabetes
title_sort protective effects of gallic acid on cardiac electrophysiology and arrhythmias during reperfusion in diabetes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556507/
https://www.ncbi.nlm.nih.gov/pubmed/31217931
http://dx.doi.org/10.22038/ijbms.2019.27563.6726
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