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The anti-infarct, antistunning and antiarrhythmic effects of oleuropein in isolated rat heart
Previous studies have reported that oleuropein, the major constituent of olive leaves, has cardioprotective effects. There is no report related to oleuropein and ischemic-reperfusion injuries (cardiac dysfunction and myocardial infarction) as well as preconditioning in rat hearts. 56 male Wistar rat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Leibniz Research Centre for Working Environment and Human Factors
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928024/ https://www.ncbi.nlm.nih.gov/pubmed/27366137 |
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author | Esmailidehaj, Mansour Rasulian, Bahram Rezvani, Mohammad Ebrahim Delfan, Bahram Mosaddeghmehrjardi, Mohammad Hossein Pourkhalili, Khalil |
author_facet | Esmailidehaj, Mansour Rasulian, Bahram Rezvani, Mohammad Ebrahim Delfan, Bahram Mosaddeghmehrjardi, Mohammad Hossein Pourkhalili, Khalil |
author_sort | Esmailidehaj, Mansour |
collection | PubMed |
description | Previous studies have reported that oleuropein, the major constituent of olive leaves, has cardioprotective effects. There is no report related to oleuropein and ischemic-reperfusion injuries (cardiac dysfunction and myocardial infarction) as well as preconditioning in rat hearts. 56 male Wistar rats were divided into 7 groups (n=8). Group 1 as the control group and groups 2 to 7 as the treatment groups that received a single dose of oleuropein (100 mg/kg, i.p.) 1, 3, 6, 12, 24 and 48 hours before the excision of the heart, respectively. After these times, their hearts were excised and subjected to 30 min regional ischemia and 120 min reperfusion under Langendorff apparatus. Electrocardiogram and intraventricular pressures were monitored and recorded throughout the procedure. Finally, infarct size was measured by triphenyltetrazolium chloride staining. Compared to the control group, oleuropein significantly reduced infarct size and reperfusion-induced cardiac dysfunction in groups 2 and 3. Oleuropein markedly attenuated both ischemic and reperfusion arrhythmias in groups 2 and 3. There was no significant difference between other groups (4 to 7) than the control group. Heart rate had no significant difference among all of the groups. These results indicate that pretreatment of rats with a single dose of intraperitoneal oleuropein could protect their heart against ischemic-reperfusion injury for at least 3 hours. However, it has no preconditioning effect, since oleuropein had not cardioprotective effects 24 hour later. |
format | Online Article Text |
id | pubmed-4928024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Leibniz Research Centre for Working Environment and Human Factors |
record_format | MEDLINE/PubMed |
spelling | pubmed-49280242016-06-30 The anti-infarct, antistunning and antiarrhythmic effects of oleuropein in isolated rat heart Esmailidehaj, Mansour Rasulian, Bahram Rezvani, Mohammad Ebrahim Delfan, Bahram Mosaddeghmehrjardi, Mohammad Hossein Pourkhalili, Khalil EXCLI J Original Article Previous studies have reported that oleuropein, the major constituent of olive leaves, has cardioprotective effects. There is no report related to oleuropein and ischemic-reperfusion injuries (cardiac dysfunction and myocardial infarction) as well as preconditioning in rat hearts. 56 male Wistar rats were divided into 7 groups (n=8). Group 1 as the control group and groups 2 to 7 as the treatment groups that received a single dose of oleuropein (100 mg/kg, i.p.) 1, 3, 6, 12, 24 and 48 hours before the excision of the heart, respectively. After these times, their hearts were excised and subjected to 30 min regional ischemia and 120 min reperfusion under Langendorff apparatus. Electrocardiogram and intraventricular pressures were monitored and recorded throughout the procedure. Finally, infarct size was measured by triphenyltetrazolium chloride staining. Compared to the control group, oleuropein significantly reduced infarct size and reperfusion-induced cardiac dysfunction in groups 2 and 3. Oleuropein markedly attenuated both ischemic and reperfusion arrhythmias in groups 2 and 3. There was no significant difference between other groups (4 to 7) than the control group. Heart rate had no significant difference among all of the groups. These results indicate that pretreatment of rats with a single dose of intraperitoneal oleuropein could protect their heart against ischemic-reperfusion injury for at least 3 hours. However, it has no preconditioning effect, since oleuropein had not cardioprotective effects 24 hour later. Leibniz Research Centre for Working Environment and Human Factors 2012-04-03 /pmc/articles/PMC4928024/ /pubmed/27366137 Text en Copyright © 2012 Esmailidehaj et al. http://www.excli.de/documents/assignment_of_rights.pdf This is an Open Access article distributed under the following Assignment of Rights http://www.excli.de/documents/assignment_of_rights.pdf. You are free to copy, distribute and transmit the work, provided the original author and source are credited. |
spellingShingle | Original Article Esmailidehaj, Mansour Rasulian, Bahram Rezvani, Mohammad Ebrahim Delfan, Bahram Mosaddeghmehrjardi, Mohammad Hossein Pourkhalili, Khalil The anti-infarct, antistunning and antiarrhythmic effects of oleuropein in isolated rat heart |
title | The anti-infarct, antistunning and antiarrhythmic effects of oleuropein in isolated rat heart |
title_full | The anti-infarct, antistunning and antiarrhythmic effects of oleuropein in isolated rat heart |
title_fullStr | The anti-infarct, antistunning and antiarrhythmic effects of oleuropein in isolated rat heart |
title_full_unstemmed | The anti-infarct, antistunning and antiarrhythmic effects of oleuropein in isolated rat heart |
title_short | The anti-infarct, antistunning and antiarrhythmic effects of oleuropein in isolated rat heart |
title_sort | anti-infarct, antistunning and antiarrhythmic effects of oleuropein in isolated rat heart |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928024/ https://www.ncbi.nlm.nih.gov/pubmed/27366137 |
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