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Effect of Lactation on myocardial vulnerability to ischemic insult in rats

BACKGROUND: Cardiovascular diseases are the leading cause of mortality and long-term disability worldwide. Various studies have suggested a protective effect of lactation in reducing the risk of cardiovascular diseases. OBJECTIVE: This study was designed to assess the effects of pregnancy and lactat...

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Autores principales: Askari, Sahar, Imani, Alireza, Sadeghipour, Hamidreza, Faghihi, Mahdieh, Edalatyzadeh, Zohreh, Choopani, Samira, Karimi, Nasser, Fatima, Sulail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cardiologia - SBC 2017
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444891/
https://www.ncbi.nlm.nih.gov/pubmed/28444063
http://dx.doi.org/10.5935/abc.20170042
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author Askari, Sahar
Imani, Alireza
Sadeghipour, Hamidreza
Faghihi, Mahdieh
Edalatyzadeh, Zohreh
Choopani, Samira
Karimi, Nasser
Fatima, Sulail
author_facet Askari, Sahar
Imani, Alireza
Sadeghipour, Hamidreza
Faghihi, Mahdieh
Edalatyzadeh, Zohreh
Choopani, Samira
Karimi, Nasser
Fatima, Sulail
author_sort Askari, Sahar
collection PubMed
description BACKGROUND: Cardiovascular diseases are the leading cause of mortality and long-term disability worldwide. Various studies have suggested a protective effect of lactation in reducing the risk of cardiovascular diseases. OBJECTIVE: This study was designed to assess the effects of pregnancy and lactation on the vulnerability of the myocardium to an ischemic insult. METHODS: Eighteen female rats were randomly divided into three groups: ischemia-reperfusion (IR), in which the hearts of virgin rats underwent IR (n = 6); lactating, in which the rats nursed their pups for 3 weeks and the maternal hearts were then submitted to IR (n = 6); and non-lactating, in which the pups were separated after birth and the maternal hearts were submitted to IR (n = 6). Outcome measures included heart rate (HR), left ventricular developed pressure (LVDP), rate pressure product (RPP), ratio of the infarct size to the area at risk (IS/AAR %), and ventricular arrhythmias - premature ventricular contraction (PVC) and ventricular tachycardia (VT). RESULTS: The IS/AAR was markedly decreased in the lactating group when compared with the non-lactating group (13.2 ± 2.5 versus 39.7 ± 3.5, p < 0.001) and the IR group (13.2 ± 2.5 versus 34.0 ± 4.7, p < 0.05). The evaluation of IR-induced ventricular arrhythmias indicated that the number of compound PVCs during ischemia, and the number and duration of VTs during ischemia and in the first 5 minutes of reperfusion in the non-lactating group were significantly (p < 0.05) higher than those in the lactating and IR groups. CONCLUSION: Lactation induced early-onset cardioprotective effects, while rats that were not allowed to nurse their pups were more susceptible to myocardial IR injury.
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spelling pubmed-54448912017-05-31 Effect of Lactation on myocardial vulnerability to ischemic insult in rats Askari, Sahar Imani, Alireza Sadeghipour, Hamidreza Faghihi, Mahdieh Edalatyzadeh, Zohreh Choopani, Samira Karimi, Nasser Fatima, Sulail Arq Bras Cardiol Original Articles BACKGROUND: Cardiovascular diseases are the leading cause of mortality and long-term disability worldwide. Various studies have suggested a protective effect of lactation in reducing the risk of cardiovascular diseases. OBJECTIVE: This study was designed to assess the effects of pregnancy and lactation on the vulnerability of the myocardium to an ischemic insult. METHODS: Eighteen female rats were randomly divided into three groups: ischemia-reperfusion (IR), in which the hearts of virgin rats underwent IR (n = 6); lactating, in which the rats nursed their pups for 3 weeks and the maternal hearts were then submitted to IR (n = 6); and non-lactating, in which the pups were separated after birth and the maternal hearts were submitted to IR (n = 6). Outcome measures included heart rate (HR), left ventricular developed pressure (LVDP), rate pressure product (RPP), ratio of the infarct size to the area at risk (IS/AAR %), and ventricular arrhythmias - premature ventricular contraction (PVC) and ventricular tachycardia (VT). RESULTS: The IS/AAR was markedly decreased in the lactating group when compared with the non-lactating group (13.2 ± 2.5 versus 39.7 ± 3.5, p < 0.001) and the IR group (13.2 ± 2.5 versus 34.0 ± 4.7, p < 0.05). The evaluation of IR-induced ventricular arrhythmias indicated that the number of compound PVCs during ischemia, and the number and duration of VTs during ischemia and in the first 5 minutes of reperfusion in the non-lactating group were significantly (p < 0.05) higher than those in the lactating and IR groups. CONCLUSION: Lactation induced early-onset cardioprotective effects, while rats that were not allowed to nurse their pups were more susceptible to myocardial IR injury. Sociedade Brasileira de Cardiologia - SBC 2017-05 /pmc/articles/PMC5444891/ /pubmed/28444063 http://dx.doi.org/10.5935/abc.20170042 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Askari, Sahar
Imani, Alireza
Sadeghipour, Hamidreza
Faghihi, Mahdieh
Edalatyzadeh, Zohreh
Choopani, Samira
Karimi, Nasser
Fatima, Sulail
Effect of Lactation on myocardial vulnerability to ischemic insult in rats
title Effect of Lactation on myocardial vulnerability to ischemic insult in rats
title_full Effect of Lactation on myocardial vulnerability to ischemic insult in rats
title_fullStr Effect of Lactation on myocardial vulnerability to ischemic insult in rats
title_full_unstemmed Effect of Lactation on myocardial vulnerability to ischemic insult in rats
title_short Effect of Lactation on myocardial vulnerability to ischemic insult in rats
title_sort effect of lactation on myocardial vulnerability to ischemic insult in rats
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444891/
https://www.ncbi.nlm.nih.gov/pubmed/28444063
http://dx.doi.org/10.5935/abc.20170042
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