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Long-term effects of early overnutrition in the heart of male adult rats: role of the renin-angiotensin system

Authors :
Luis Monge
Gonzalo Carreño-Tarragona
Juan Carlos Figueras
Sara Amor
Miriam Granado
Nuria Fernández
Angel Luis García-Villalón
UAM. Departamento de Fisiología
Source :
Biblos-e Archivo. Repositorio Institucional de la UAM, instname, PLoS ONE, PLoS ONE, Vol 8, Iss 6, p e65172 (2014)
Publication Year :
2013
Publisher :
Public Library of Science, 2013.

Abstract

To analyze the long-term effects of early overfeeding on the heart and coronary circulation, the effect of ischemia-reperfusion (I/R) and the role of the renin-angiotensin system (RAS) was studied in isolated hearts from control and overfed rats during lactation. On the day of birth litters were adjusted to twelve pups per mother (controls) or to three pups per mother (overfed). At 5 months of age, the rats from reduced litters showed higher body weight and body fat than the controls. The hearts from these rats were perfused in a Langendorff system and subjected to 30 min of ischemia followed by 15 min of reperfusion (I/R). The myocardial contractility (dP/dt) and the coronary vasoconstriction to angiotensin II were lower, and the expression of the apoptotic marker was higher, in the hearts from overfed rats compared to controls. I/R reduced the myocardial contractily, the coronary vasoconstriction to angiotensin II and the vasodilatation to bradykinin, and increased the expression of (pro)renin receptor and of apoptotic and antiapoptotic markers, in both experimental groups. I/R also increased the expression of angiotensinogen in control but not in overfed rats. In summary, the results of this study suggest that early overnutrition induces reduced activity of the RAS and impairment of myocardial and coronary function in adult life, due to increased apoptosis. Ischemia-reperfusion produced myocardial and coronary impairment and apoptosis, which may be related to activation of RAS in control but not in overfed rats, and there may be protective mechanisms in both experimental groups<br />This work was financed by Fundación Mapfre (2011) and Fondo de Investigaciones Sanitarias (PS09/00394

Details

Database :
OpenAIRE
Journal :
Biblos-e Archivo. Repositorio Institucional de la UAM, instname, PLoS ONE, PLoS ONE, Vol 8, Iss 6, p e65172 (2014)
Accession number :
edsair.doi.dedup.....ea0537abdb5cf674f4886a7eedb1d786