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American Physiological Society, Journal of Applied Physiology, 3(120), p. 344-350, 2016

DOI: 10.1152/japplphysiol.00246.2015

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Maternal Protein Restriction Compromises Myocardial Contractility in the Young Adult Rat by Changing Proteins Involved in Calcium Handling

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Maternal protein restriction (MPR) during pregnancy is associated with increased cardiovascular risk in the offspring in adulthood. In this study we evaluated the the cardiac function of young male rats born from mothers subjected to MPR during pregnancy, focusing on the myocardial mechanics and calcium handling proteins. After weaning, rats received normal diet until three months old, when the following parameters were assessed: arterial and left ventricular hemodynamics and in vitro cardiac contractility in isolated papillary muscles. The body weight was lower and arterial pressure higher in the MPR group compared to young adult offspring of female rats that received standard diet (controls); and left ventricle time derivatives increased in the MPR group. The force developed by the cardiac muscle was similar; but time to peak and relaxation time were longer, and the derivatives of force were depressed in the MPR. In addition, MPR group exhibited decreased post-pause potentiation of force, suggesting reduced reuptake function of the sarcoplasmic reticulum. Corroborating, the myocardial content of SERCA-2a and phosphoryled PLB-Ser16 / total PLB ration was decreased and sodium-calcium exchanger was increased in the MPR group. The contraction dependent of transsarcolemmal influx of calcium was higher in MPR if compared to the control group. In summary, young rats born from mothers subjected to protein restriction during pregnancy exhibit changes in the myocardial mechanics with altered expression of calcium handling proteins, reinforcing the hypothesis that maternal malnutrition is related to increased cardiovascular risk in its offspring, not only for hypertension, but also cardiac dysfunction.