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Published on: March 13, 2014
Phospholipid profile of developing heart of rats exposed to low-protein diet in pregnancy
Paramjit S Tappia1, Mohinder S Nijjar, Aric Mahay
1Cardiac Membrane Biology Laboratory, Institute of Cardiovascular Sciences, St. Boniface Hospital Research Centre (R3020), 351 Tache Ave., Winnipeg, Manitoba, Canada R2H 2A6. ptappia@sbrc.ca
Insights
Restricted maternal protein intake during pregnancy alters offspring heart phospholipid and fatty acid profiles. This low-protein diet impacts cardiac metabolism, potentially affecting neonatal heart function.
Area of Science:
- Cardiovascular Biology
- Nutritional Science
- Developmental Biology
Background:
- Myocardial phospholipid and fatty acid composition are crucial for heart function.
- Limited data exists on the impact of maternal dietary protein restriction on fetal heart development.
- Understanding these effects is vital for optimizing prenatal nutrition and infant cardiac health.
Purpose of the Study:
- To investigate the effects of maternal low-protein (LP) diet on myocardial phospholipid and fatty acid profiles in male offspring.
- To assess changes in cardiac transcription factors regulating metabolism under LP diet conditions.
- To determine potential implications for neonatal heart metabolism.
Main Methods:
- Pregnant dams were fed either a normal (180 g/kg) or low-protein (90 g/kg) casein diet for 2 weeks pre-mating and throughout gestation.
- Myocardial phospholipid and fatty acid content of male offspring hearts were analyzed.
- mRNA levels of cardiac transcription factors, including myocyte enhancer factor-2C and peroxisome proliferator-activated receptor-alpha, were assessed.
Main Results:
- Maternal LP diet led to increased lysophosphatidylcholine, phosphatidylserine, and sphingomyelin in offspring hearts.
- Significant reductions in saturated fatty acids (myristate, palmitate, stearate) and increases in unsaturated fatty acids (linoleate, arachidonate, decosahexanoate) were observed.
- LP group showed decreased myocyte enhancer factor-2C mRNA and increased peroxisome proliferator-activated receptor-alpha mRNA levels.
Conclusions:
- Maternal low-protein diet significantly alters the phospholipid and fatty acid composition of the developing heart.
- These alterations in cardiac lipid profiles and transcription factor expression may influence neonatal heart metabolism.
- Findings highlight the critical role of maternal nutrition in fetal cardiac development and long-term health.
Abstract:
Although the myocardial phospholipid and fatty acid content have profound effects on the heart function, very little information is available on the effects of restricted maternal protein intake during pregnancy on the phospholipid profile and fatty acid content of the developing heart. The present study was therefore undertaken to examine the effect of pregnant dams fed diets containing either 180 (normal) or 90 (low) g/kg casein diet for 2 wk before mating and throughout pregnancy on myocardial phospholipid and fatty acid content of male offspring. Whereas no changes in phosphatidylcholine and phosphatidylethanolamine were detected, increases in lysophosphatidylcholine, phosphatidylserine, and sphingomyelin were seen in the hearts of offspring in the low-protein (LP) group. Analysis of cardiac fatty acids revealed that although the saturated fatty acid (myristate, palmitate, and stearate) levels were significantly reduced, the unsaturated fatty acid (linoleate, arachidonate, and decosahexanoate) levels were significantly increased in the developing heart in the LP group. Furthermore, assessment of nuclear transcription factors involved in regulation of cardiac metabolism revealed a decrease in myocyte enhancer factor-2C mRNA levels in the LP group, whereas an increase in the mRNA amount of peroxisome proliferator-activated receptor-alpha was observed in this group. These results demonstrate that maternal LP diet can induce changes in the phospholipid profile and fatty acid content of the developing heart, which may have implications for metabolism of the neonatal heart.
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