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Effects of short-term administration of estradiol on reperfusion arrhythmias in rats of different ages

Little is known about age-related differences in short-term effects of estradiol on ischemia-reperfusion (I/R) insults. The present study was designed to evaluate the effects of short-term treatment with estradiol on reperfusion arrhythmias in isolated hearts of 6-7-week-old and 12-14-month-old fema...

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Autores principales: Savergnini, S.Q., Reis, A.M., Santos, R.A.S., Santos, P.E.B., Ferreira, A.J., Almeida, A.P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Medicina Tropical 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854225/
https://www.ncbi.nlm.nih.gov/pubmed/23108785
http://dx.doi.org/10.1590/S0100-879X2012007500169
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author Savergnini, S.Q.
Reis, A.M.
Santos, R.A.S.
Santos, P.E.B.
Ferreira, A.J.
Almeida, A.P.
author_facet Savergnini, S.Q.
Reis, A.M.
Santos, R.A.S.
Santos, P.E.B.
Ferreira, A.J.
Almeida, A.P.
author_sort Savergnini, S.Q.
collection PubMed
description Little is known about age-related differences in short-term effects of estradiol on ischemia-reperfusion (I/R) insults. The present study was designed to evaluate the effects of short-term treatment with estradiol on reperfusion arrhythmias in isolated hearts of 6-7-week-old and 12-14-month-old female rats. Wistar rats were sham-operated, ovariectomized and treated with vehicle or ovariectomized and treated with 17β-estradiol (E(2); 5 µg·100 g(−1)·day(−1)) for 4 days. Hearts were perfused by the Langendorff technique. Reperfusion arrhythmias, i.e., ventricular tachycardia and/or ventricular fibrillation, were induced by 15 min of left coronary artery ligation and 30 min of reperfusion. The duration and incidence of I/R arrhythmias were significantly higher in young rats compared to middle-aged rats (arrhythmia severity index: 9.4 ± 1.0 vs 3.0 ± 0.3 arbitrary units, respectively, P < 0.05). In addition, middle-aged rats showed lower heart rate, systolic tension and coronary flow. Four-day E(2) treatment caused an increase in uterine weight. Although E(2) administration had no significant effect on the duration of I/R arrhythmias in middle-aged rats, it induced a marked reduction in the rhythm disturbances of young rats accompanied by a decrease in heart rate of isolated hearts. Also, this reduction was associated with an increase in QT interval. No significant changes were observed in the QT interval of middle-aged E(2)-treated rats. These data demonstrate that short-term estradiol treatment protects against I/R arrhythmias in hearts of young female rats. The anti-arrhythmogenic effect of estradiol might be related to a lengthening of the QT interval.
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spelling pubmed-38542252013-12-16 Effects of short-term administration of estradiol on reperfusion arrhythmias in rats of different ages Savergnini, S.Q. Reis, A.M. Santos, R.A.S. Santos, P.E.B. Ferreira, A.J. Almeida, A.P. Braz J Med Biol Res Short Communication Little is known about age-related differences in short-term effects of estradiol on ischemia-reperfusion (I/R) insults. The present study was designed to evaluate the effects of short-term treatment with estradiol on reperfusion arrhythmias in isolated hearts of 6-7-week-old and 12-14-month-old female rats. Wistar rats were sham-operated, ovariectomized and treated with vehicle or ovariectomized and treated with 17β-estradiol (E(2); 5 µg·100 g(−1)·day(−1)) for 4 days. Hearts were perfused by the Langendorff technique. Reperfusion arrhythmias, i.e., ventricular tachycardia and/or ventricular fibrillation, were induced by 15 min of left coronary artery ligation and 30 min of reperfusion. The duration and incidence of I/R arrhythmias were significantly higher in young rats compared to middle-aged rats (arrhythmia severity index: 9.4 ± 1.0 vs 3.0 ± 0.3 arbitrary units, respectively, P < 0.05). In addition, middle-aged rats showed lower heart rate, systolic tension and coronary flow. Four-day E(2) treatment caused an increase in uterine weight. Although E(2) administration had no significant effect on the duration of I/R arrhythmias in middle-aged rats, it induced a marked reduction in the rhythm disturbances of young rats accompanied by a decrease in heart rate of isolated hearts. Also, this reduction was associated with an increase in QT interval. No significant changes were observed in the QT interval of middle-aged E(2)-treated rats. These data demonstrate that short-term estradiol treatment protects against I/R arrhythmias in hearts of young female rats. The anti-arrhythmogenic effect of estradiol might be related to a lengthening of the QT interval. Sociedade Brasileira de Medicina Tropical 2012-11-01 /pmc/articles/PMC3854225/ /pubmed/23108785 http://dx.doi.org/10.1590/S0100-879X2012007500169 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Savergnini, S.Q.
Reis, A.M.
Santos, R.A.S.
Santos, P.E.B.
Ferreira, A.J.
Almeida, A.P.
Effects of short-term administration of estradiol on reperfusion arrhythmias in rats of different ages
title Effects of short-term administration of estradiol on reperfusion arrhythmias in rats of different ages
title_full Effects of short-term administration of estradiol on reperfusion arrhythmias in rats of different ages
title_fullStr Effects of short-term administration of estradiol on reperfusion arrhythmias in rats of different ages
title_full_unstemmed Effects of short-term administration of estradiol on reperfusion arrhythmias in rats of different ages
title_short Effects of short-term administration of estradiol on reperfusion arrhythmias in rats of different ages
title_sort effects of short-term administration of estradiol on reperfusion arrhythmias in rats of different ages
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854225/
https://www.ncbi.nlm.nih.gov/pubmed/23108785
http://dx.doi.org/10.1590/S0100-879X2012007500169
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