Details

Autor(en) / Beteiligte

• Chang, Eileen I.
• Stremming, Jane
• Knaub, Leslie A.
• Wesolowski, Stephanie R.
• Rozance, Paul J.
• Sucharov, Carmen C.
• Reusch, Jane E. B.
• Brown, Laura D.

Titel

Mitochondrial respiration is lower in the intrauterine growth‐restricted fetal sheep heart

Ist Teil von

• The Journal of physiology, 2024-06, Vol.602 (12), p.2697-2715

Ort / Verlag

England: Wiley Subscription Services, Inc

Erscheinungsjahr

2024

Quelle

Wiley Online Library Journals Frontfile Complete

Beschreibungen/Notizen

• Fetuses affected by intrauterine growth restriction have an increased risk of developing heart disease and failure in adulthood. Compared with controls, late gestation intrauterine growth‐restricted (IUGR) fetal sheep have fewer binucleated cardiomyocytes, reflecting a more immature heart, which may reduce mitochondrial capacity to oxidize substrates. We hypothesized that the late gestation IUGR fetal heart has a lower capacity for mitochondrial oxidative phosphorylation. Left (LV) and right (RV) ventricles from IUGR and control (CON) fetal sheep at 90% gestation were harvested. Mitochondrial respiration (states 1–3, LeakOmy, and maximal respiration) in response to carbohydrates and lipids, citrate synthase (CS) activity, protein expression levels of mitochondrial oxidative phosphorylation complexes (CI–CV), and mRNA expression levels of mitochondrial biosynthesis regulators were measured. The carbohydrate and lipid state 3 respiration rates were lower in IUGR than CON, and CS activity was lower in IUGR LV than CON LV. However, relative CII and CV protein levels were higher in IUGR than CON; CV expression level was higher in IUGR than CON. Genes involved in lipid metabolism had lower expression in IUGR than CON. In addition, the LV and RV demonstrated distinct differences in oxygen flux and gene expression levels, which were independent from CON and IUGR status. Low mitochondrial respiration and CS activity in the IUGR heart compared with CON are consistent with delayed cardiomyocyte maturation, and CII and CV protein expression levels may be upregulated to support ATP production. These insights will provide a better understanding of fetal heart development in an adverse in utero environment. Key points Growth‐restricted fetuses have a higher risk of developing and dying from cardiovascular diseases in adulthood. Mitochondria are the main supplier of energy for the heart. As the heart matures, the substrate preference of the mitochondria switches from carbohydrates to lipids. We used a sheep model of intrauterine growth restriction to study the capacity of the mitochondria in the heart to produce energy using either carbohydrate or lipid substrates by measuring how much oxygen was consumed. Our data show that the mitochondria respiration levels in the growth‐restricted fetal heart were lower than in the normally growing fetuses, and the expression levels of genes involved in lipid metabolism were also lower. Differences between the right and left ventricles that are independent of the fetal growth restriction condition were identified. These results indicate an impaired metabolic maturation of the growth‐restricted fetal heart associated with a decreased capacity to oxidize lipids postnatally. figure legend Intrauterine growth restriction (IUGR) during fetal development can affect cardiovascular health in adulthood. Mitochondria produce ATP via oxidative phosphorylation as the main energy source of the heart. As the fetal heart matures and the mononucleated cardiomyocytes differentiate to binucleated cardiomyocytes, the mitochondria switch from anaerobic glycolysis to beta‐oxidation. Late gestation IUGR fetal sheep compared with controls have fewer binucleated cardiomyocytes, which may reduce mitochondrial capacity to oxidize substrates. The present study used a sheep model of IUGR to study the capacity of the mitochondria in the heart to produce energy using either carbohydrate or lipid substrates. We show that the mitochondria respiration levels in the growth‐restricted fetal heart were lower than in normally growing fetuses, and the expression levels of genes involved in lipid metabolism were also lower. These results suggest an impaired metabolic maturation of the growth‐restricted fetal heart associated with a decreased capacity to oxidize lipids.