Early Postnatal Cardiomyocyte Proliferation Requires High Oxidative Energy Metabolism

• Published in: Scientific reports Vol. 7; no. 1; pp. 15434 - 11
• Main Authors: de Carvalho, Ana Elisa Teófilo Saturi, Bassaneze, Vinícius, Forni, Maria Fernanda, Keusseyan, Aline Alfonso, Kowaltowski, Alicia Juliana, Krieger, José Eduardo
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 13.11.2017; Nature Publishing Group
• Subjects: 13/106; 14/1; 14/19; 38/91; 631/443/592/2725; 692/4019/592/2725; Animals; Animals, Newborn; Birth; Cardiomyocytes; Cell proliferation; Cell Proliferation - physiology; Cells, Cultured; Electron transport; Energy demand; Energy metabolism; Energy Metabolism - physiology; Gene expression; Glycolysis; Glycolysis - physiology; Heart; Heart - growth & development; Heart diseases; Hemodynamics; Humanities and Social Sciences; Metabolism; Mitochondria; Mitochondria - chemistry; Mitochondria - metabolism; multidisciplinary; Myocytes, Cardiac - cytology; Myocytes, Cardiac - metabolism; Neonates; Oxidation-Reduction; Oxidative metabolism; Oxidative Stress - physiology; Oxygen - analysis; Oxygen - metabolism; Primary Cell Culture; Rats; Rats, Wistar; Respiration; Science; Science (multidisciplinary)
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-017-15656-3

Cardiac energy metabolism must cope with early postnatal changes in tissue oxygen tensions, hemodynamics, and cell proliferation to sustain development. Here, we tested the hypothesis that proliferating neonatal cardiomyocytes are dependent on high oxidative energy metabolism. We show that energy-related gene expression does not correlate with functional oxidative measurements in the developing heart. Gene expression analysis suggests a gradual overall upregulation of oxidative-related genes and pathways, whereas functional assessment in both cardiac tissue and cultured cardiomyocytes indicated that oxidative metabolism decreases between the first and seventh days after birth. Cardiomyocyte extracellular flux analysis indicated that the decrease in oxidative metabolism between the first and seventh days after birth was mostly related to lower rates of ATP-linked mitochondrial respiration, suggesting that overall energetic demands decrease during this period. In parallel, the proliferation rate was higher for early cardiomyocytes. Furthermore, in vitro nonlethal chemical inhibition of mitochondrial respiration reduced the proliferative capacity of early cardiomyocytes, indicating a high energy demand to sustain cardiomyocyte proliferation. Altogether, we provide evidence that early postnatal cardiomyocyte proliferative capacity correlates with high oxidative energy metabolism. The energy requirement decreases as the proliferation ceases in the following days, and both oxidative-dependent metabolism and anaerobic glycolysis subside.