Substrate metabolism in the developing heart

Handbook of Physiology.

Plum, F. (1960) · Archives of Neurology · doi:10.1001/archneur.1960.03840090124020 · Cited by 10,388 · see citing works

Cardiovascular System

Stoschitzky, K. (2000) · Handbooks of pharmacology and toxicology · doi:10.1201/9781420036961.ch18 · Cited by 3,258 · see citing works

Relationship Between Carbohydrate and Lipid Metabolism and the Energy Balance of Heart Muscle

Neely, J. R., & Morgan, H. E. (1974) · Annual Review of Physiology · doi:10.1146/annurev.ph.36.030174.002213 · Cited by 1,266 · see citing works

Handbook of Physiology—The Cardiovascular System

Guyton, A. C. (1985) · Critical Care Medicine · doi:10.1097/00003246-198505000-00025 · Cited by 1,153 · see citing works

Foetal and Neonatal Physiology

Comline, K. S., Cross, K. W., Dawes, G. S., & Nathanielsz, P. W. (1973) · Cited by 750 · see citing works

Lipid-membrane interactions and the pathogenesis of ischemic damage in the myocardium.

Katz, A., & Messineo, F. C. (1981) · Circulation Research · doi:10.1161/01.res.48.1.1 · Cited by 608 · see citing works

Role of glycolytic products in damage to ischemic myocardium. Dissociation of adenosine triphosphate levels and recovery of function of reperfused ischemic hearts.

Neely, J. R., & Grotyohann, L. W. (1984) · Circulation Research · doi:10.1161/01.res.55.6.816 · Cited by 579 · see citing works

The pharmacology of dichloroacetate

Stacpoole, P. W. (1989) · Metabolism · doi:10.1016/0026-0495(89)90051-6 · Cited by 485 · see citing works

Metabolism of the heart in health and disease. Part I

Opie, L. H. (1968) · American Heart Journal · doi:10.1016/0002-8703(68)90168-3 · Cited by 418 · see citing works

Glycolysis preferentially inhibits ATP-sensitive K+ channels in isolated guinea pig cardiac myocytes.

Weiss, J., & Lamp, S. (1987) · Science · doi:10.1126/science.2443972 · Cited by 401 · see citing works

Ischemic contracture of the myocardium: Mechanisms and prevention

Hearse, D. J., Garlick, P. B., & Humphrey, S. M. (1977) · The American Journal of Cardiology · doi:10.1016/s0002-9149(77)80212-9 · Cited by 396 · see citing works

Carbohydrate metabolism in pregnancy

Herrera, E., Knopp, R. H., & Freinkel, N. (1969) · Journal of Clinical Investigation · doi:10.1172/jci106192 · Cited by 381 · see citing works

GLYCOGEN RFSERVES AND THEIR CHANGES AT BIRTH AND IN ANOXIA

Shelley, H. J. (1961) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a069888 · Cited by 371 · see citing works

Regulation of ketogenesis and the renaissance of carnitine palmitoyltransferase

McGarry, J., Woeltje, K. F., Kuwajima, M., & Foster, D. W. (1989) · Diabetes/Metabolism Reviews · doi:10.1002/dmr.5610050305 · Cited by 359 · see citing works

Developmental changes in energy substrate use by the heart

Lopaschuk, G. D., Collins-Nakai, R. L., & Itoi, T. (1992) · Cardiovascular Research · doi:10.1093/cvr/26.12.1172 · Cited by 325 · see citing works

Control of maximum rates of glycolysis in rat cardiac muscle.

Kobayashi, K., & Neely, J. R. (1979) · Circulation Research · doi:10.1161/01.res.44.2.166 · Cited by 313 · see citing works

Functional Coupling Between Glycolysis and Sarcoplasmic Reticulum Ca 2+ Transport

Xu, K. Y., Zweier, J. L., & Becker, L. C. (1995) · Circulation Research · doi:10.1161/01.res.77.1.88 · Cited by 308 · see citing works

Effects of excess free fatty acids on mechanical and metabolic function in normal and ischemic myocardium in swine.

Liedtke, A. J., Nellis, S. H., & Neely, J. R. (1978) · Circulation Research · doi:10.1161/01.res.43.4.652 · Cited by 288 · see citing works

Etomoxir, a carnitine palmitoyltransferase I inhibitor, protects hearts from fatty acid-induced ischemic injury independent of changes in long chain acylcarnitine.

Lopaschuk, G. D., Wall, S. R., Olley, P. M., & Davies, N. J. (1988) · Circulation Research · doi:10.1161/01.res.63.6.1036 · Cited by 284 · see citing works

Effects of acidosis and ischemia on contractility and intracellular pH of rat heart.

Steenbergen, C., Deleeuw, G., Rich, T. L., & WILLIAMSON, J. R. (1977) · Circulation Research · doi:10.1161/01.res.41.6.849 · Cited by 268 · see citing works

Invertebrate Facultative Anaerobiosis

Hochachka, P. W., & Mustafa, T. (1972) · Science · doi:10.1126/science.178.4065.1056 · Cited by 260 · see citing works

Glycolysis is predominant source of myocardial ATP production immediately after birth

Lopaschuk, G. D., Spafford, M. A., & Marsh, D. R. (1991) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1991.261.6.h1698 · Cited by 258 · see citing works

Functional compartmentation of glycolytic versus oxidative metabolism in isolated rabbit heart.

Weiss, J. N., & Hiltbrand, B. (1985) · Journal of Clinical Investigation · doi:10.1172/jci111718 · Cited by 251 · see citing works

The Use of NMR Spectroscopy for the Understanding of Disease

Radda, G. K. (1986) · Science · doi:10.1126/science.3726553 · Cited by 249 · see citing works

Lactate production under fully aerobic conditions: the lactate shuttle during rest and exercise.

Brooks, G. A. (1986) · PubMed · Cited by 235 · see citing works

Protective effect of increased glycolytic substrate against systolic and diastolic dysfunction and increased coronary resistance from prolonged global underperfusion and reperfusion in isolated rabbit hearts perfused with erythrocyte suspensions.

Eberli, F. R., Weinberg, E. O., Grice, W. N., Horowitz, G., & Apstein, C. S. (1991) · Circulation Research · doi:10.1161/01.res.68.2.466 · Cited by 219 · see citing works

NMR Studies of Tissue Metabolism

Gadian, D. G., & Radda, G. K. (1981) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.50.070181.000441 · Cited by 213 · see citing works

An Introduction to Fetal Physiology

Battaglia, F. C., & Meschia, G. (1986) · Medical Entomology and Zoology · Cited by 202 · see citing works

Metabolic responses to cardiac hypoxia. Increased production of succinate by rabbit papillary muscles.

Taegtmeyer, H. (1978) · Circulation Research · doi:10.1161/01.res.43.5.808 · Cited by 201 · see citing works

Developmental and Physiological Correlates of Cardiac Muscle

Lieberman, M., Sano, T., & Pollack, G. H. (1977) · Anesthesiology · doi:10.1097/00000542-197710000-00026 · Cited by 189 · see citing works

Dichloroacetate stimulation of glucose oxidation improves recovery of ischemic rat hearts

McVeigh, J., & Lopaschuk, G. D. (1990) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1990.259.4.h1079 · Cited by 184 · see citing works

Carbohydrate metabolism in pregnancy

Phelps, R. L., Metzger, B. E., & Freinkel, N. (1981) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(81)90731-6 · Cited by 181 · see citing works

Multiple end products of anaerobiosis in diving vertebrates

Hochachka, P. W., Owen, T. G., Allen, J. F., & WHITTOW, G. C. (1975) · Comparative Biochemistry and Physiology Part B Comparative Biochemistry · doi:10.1016/0305-0491(75)90292-8 · Cited by 180 · see citing works

Glucose flux rate regulates onset of ischemic contracture in globally underperfused rat hearts.

Owen, P., Dennis, S. C., & Opie, L. H. (1990) · Circulation Research · doi:10.1161/01.res.66.2.344 · Cited by 171 · see citing works

Effects of ventricular pressure development and palmitate on glucose transport

Neely, J. R., Bowman, R. L., & Morgan, H. E. (1969) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1969.216.4.804 · Cited by 171 · see citing works

Preferential uptake of lactate by the normal myocardium in dogs

Drake, A. J., HAINES, J. R., & Noble, M. I. M. (1980) · Cardiovascular Research · doi:10.1093/cvr/14.2.65 · Cited by 168 · see citing works

Carbohydrate Metabolism in Pregnancy. XVII. Diurnal Profiles of Plasma Glucose, Insulin, Free Fatty Acids, Triglycerides, Cholesterol, and Individual Amino Acids in Late Normal Pregnancy

PHELPS, R. L., Metzger, B. E., Freinkel, N., & Bassell, G. M. (1981) · Obstetric Anesthesia Digest · doi:10.1097/00132582-198112000-00002 · Cited by 161 · see citing works

Metabolism during fetal life: a functional assessment of metabolic development.

Jones, C. T., & Rolph, T. (1985) · Physiological Reviews · doi:10.1152/physrev.1985.65.2.357 · Cited by 159 · see citing works

Myocardial oxygen and carbohydrate consumption in fetal lambs in utero and in adult sheep

Fisher, D. J., Heymann, M. A., & Rudolph, A. M. (1980) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1980.238.3.h399 · Cited by 157 · see citing works

Putative Membrane Fatty Acid Translocase and Cytoplasmic Fatty-Acid-Binding Protein Are Co-expressed in Rat Heart and Skeletal Muscles

van Nieuwenhoven, F. A., Verstijnen, C. P. H. J., Abumrad, N. A., Willemsen, P. H. M., Vaneys, G. J. J. M., Vandervusse, G. J., & Glatz, J. F. C. (1995) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1995.1250 · Cited by 155 · see citing works

Cellular energy metabolism during fetal development

Warshaw, J. B. (1972) · Developmental Biology · doi:10.1016/0012-1606(72)90001-2 · Cited by 150 · see citing works

A relationship between adenosine triphosphate, glycolysis and ischaemic contracture in the isolated rat heart

BRICKNELL, O. L. (1981) · Journal of Molecular and Cellular Cardiology · doi:10.1016/0022-2828(81)90292-3 · Cited by 150 · see citing works

Maternal-fetal carnitine relationship and neonatal ketosis in the rat.

Robles-Valdés, C., McGarry, J., & Foster, D. W. (1976) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)33051-x · Cited by 147 · see citing works

[25] Pyruvate kinase isozymes from rat

Imamura, K., & Tanaka, T. (1982) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(82)90121-5 · Cited by 142 · see citing works

Acetyl-CoA carboxylase involvement in the rapid maturation of fatty acid oxidation in the newborn rabbit heart.

Lopaschuk, G. D., Witters, L. A., Itoi, T., Barr, R. L., & Barr, A. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)47327-9 · Cited by 137 · see citing works

Developmental changes in myocardial mechanical function and subcellular organelles

Nakanishi, T., & JARMAKANI, J. M. M. (1984) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1984.246.4.h615 · Cited by 131 · see citing works

Development and regulation of glucose transporter and hexokinase expression in rat

Postic, C., Leturque, A., Printz, R. L., MAULARD, P., Loizeau, M., Granner, D. K., & Girard, J. R. (1994) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1994.266.4.e548 · Cited by 127 · see citing works

ATP synthesis kinetics and mitochondrial function in the postischemic myocardium as studied by 31P NMR.

Sako, E. Y., Kingsley-Hickman, P. B., From, A. H. L., Foker, J. E., & Uǧurbil, K. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)38013-x · Cited by 110 · see citing works

Carbohydrate and Fatty Acid Metabolism

Reid, E. (1965) · Elsevier eBooks · doi:10.1016/b978-1-4832-0024-8.50009-7 · Cited by 110 · see citing works

Perinatal hypothyroidism impairs the normal transition of GLUT4 and GLUT1 glucose transporters from fetal to neonatal levels in heart and brown adipose tissue. Evidence for tissue-specific regulation of GLUT4 expression by thyroid hormone.

Castelló, A., Rodrı́guez-Manzaneque, J. C., Camps, M., Pérez‐Castillo, A., Testar, X., Palacı́n, M., Santos, Á., & Zorzano, A. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)37547-6 · Cited by 109 · see citing works

Effects of ischemia and reperfusion on pyruvate dehydrogenase activity in isolated rat hearts

Kobayashi, K., & Neely, J. R. (1983) · Journal of Molecular and Cellular Cardiology · doi:10.1016/0022-2828(83)90320-6 · Cited by 109 · see citing works

Foetal and neonatal physiology

Chesley, L. C. (1968) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(68)90548-6 · Cited by 108 · see citing works

Effect of hypoxia on mechanical function in the neonatal mammalian heart

JARMAKANI, J. M. M., Nakazawa, M., Nagatomo, T., & LANGER, G. A. (1978) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1978.235.5.h469 · Cited by 108 · see citing works

Effect of hypoxia on myocardial high-energy phosphates in the neonatal mammalian heart

JARMAKANI, J. M. M., Nagatomo, T., Nakazawa, M., & LANGER, G. A. (1978) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1978.235.5.h475 · Cited by 108 · see citing works

Transfer of free fatty acids across the primate placenta

Portman, O. W., Behrman, R. E., & Soltys, P. A. (1969) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1969.216.1.143 · Cited by 106 · see citing works

THE RATE OF DECLINE IN RESISTANCE TO ANOXIA OF RABBITS, DOGS AND GUINEA PIGS FROM THE ONSET OF VIABILITY TO ADULT LIFE

Glass, H. G., Snyder, F. F., & Webster, E. (1944) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1944.140.5.609 · Cited by 106 · see citing works

Binding of glycolytic enzymes to cardiac sarcolemmal and sarcoplasmic reticular membranes.

Pierce, G. N., & Philipson, K. D. (1985) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)88860-3 · Cited by 105 · see citing works

Enhanced mechanical recovery of anoxic and ischemic myocardium by amino acid perfusion

Rau, E. E., Shine, K. I., Gervais, A., Douglas, A., & Amos, E. C. (1979) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1979.236.6.h873 · Cited by 104 · see citing works

Effect of Supine Exercise on Left Ventricular Volume and Oxygen Consumption in Man

Gorlin, R., Cohen, L. S., ELLIOTT, W., KLEIN, M. D., & Lane, F. J. (1965) · Circulation · doi:10.1161/01.cir.32.3.361 · Cited by 98 · see citing works

Ischemic contracture begins when anaerobic glycolysis stops: a 31P-NMR study of isolated rat hearts

Kingsley, P. B., Sako, E. Y., Yang, M. Q., Zimmer, S. D., Uǧurbil, K., Foker, J. E., & From, A. H. L. (1991) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1991.261.2.h469 · Cited by 95 · see citing works

Energy substrate utilization by isolated working hearts from newborn rabbits

Lopaschuk, G. D., & Spafford, M. A. (1990) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1990.258.5.h1274 · Cited by 91 · see citing works

Some aspects of foetal and uteroplacental metabolism in cows with indwelling umbilical and uterine vascular catheters.

Comline, R. S., & Silver, M. (1976) · The Journal of Physiology · doi:10.1113/jphysiol.1976.sp011532 · Cited by 90 · see citing works

Changes in mitochondrial respiratory chain proteins during perinatal development. Evidence of the importance of environmental oxygen tension

Hallman, M. (1971) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(71)90040-5 · Cited by 87 · see citing works

Placental transport of free palmitic and linoleic acids in the guinea pig

Hershfield, M. S., & Nemeth, A. M. (1968) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)42724-5 · Cited by 87 · see citing works

Myocardial Consumption of Oxygen and Carbohydrates in Newborn Sheep

Fisher, D. J., Heymann, M. A., & Rudolph, A. M. (1981) · Pediatric Research · doi:10.1203/00006450-198105000-00003 · Cited by 85 · see citing works

CELLULAR ENERGY METABOLISM DURING FETAL DEVELOPMENT

Warshaw, J. B., & Terry, M. L. (1970) · The Journal of Cell Biology · doi:10.1083/jcb.44.2.354 · Cited by 83 · see citing works

Influence of Glucose on the Transmembrane Action Potential of Anoxic Papillary Muscle

MacLeod, D. P., & Daniel, E. E. (1965) · The Journal of General Physiology · doi:10.1085/jgp.48.5.887 · Cited by 81 · see citing works

Lactate Metabolism of Isolated, Perfused Fetal, and Newborn Pig Hearts

Werner, J. C., & Sicard, R. E. (1987) · Pediatric Research · doi:10.1203/00006450-198711000-00016 · Cited by 81 · see citing works

Blood sugars and tissue carbohydrate in foetal and infant lambs and rhesus monkeys

Shelley, H. J. (1960) · The Journal of Physiology · doi:10.1113/jphysiol.1960.sp006553 · Cited by 81 · see citing works

Developmental changes in reperfusion injury

Pridjian, A. K., Levitsky, S., Krukenkamp, I. B., Silverman, N. A., & Feinberg, H. (1987) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/s0022-5223(19)36420-7 · Cited by 78 · see citing works

The Role of Lactate as an Energy Substrate for the Brain during the Early Neonatal Period

Medina, J. M. (2009) · Biology of the Neonate · doi:10.1159/000242176 · Cited by 76 · see citing works

Perinatal Changes in Glycolytic Function in Response to Hypoxia in the Incubated or Perfused Rat Heart

Hoerter, J. A., & OPIE, L. (2009) · Biology of the Neonate · doi:10.1159/000241064 · Cited by 76 · see citing works

Studies of myocardial protection in the immature heart

Julia, P. L., Kofsky, E. R., Buckberg, G. D., Young, H., & Bugyi, H. I. (1991) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/s0022-5223(19)36789-3 · Cited by 76 · see citing works

Fetal myocardial oxygen and carbohydrate consumption during acutely induced hypoxemia

Fisher, D. J., Heymann, M. A., & Rudolph, A. M. (1982) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1982.242.4.h657 · Cited by 75 · see citing works

Relative vulnerability of neonatal and adult hearts to ischemic injury.

Wittnich, C., Peniston, C. M., Ianuzzo, C. D., Abel, J. G., & Salerno, T. A. (1987) · PubMed · Cited by 74 · see citing works

Postnatal development of palmitate oxidation and mitochondrial enzyme activities in rat cardiac and skeletal muscle

Glatz, J. F. C., & Veerkamp, J. H. (1982) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(82)90042-x · Cited by 73 · see citing works

Carnitine palmitoyltransferase in bovine fetal heart mitochondria

Tomec, R. J., & Hoppel, C. L. (1975) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(75)90169-1 · Cited by 73 · see citing works

The effects of inhibition of oxidative phosphorylation and glycolysis on contractility and high-energy phosphate content in cultured chick heart cells.

Doorey, A. J., & Barry, W. H. (1983) · Circulation Research · doi:10.1161/01.res.53.2.192 · Cited by 71 · see citing works

Studies of myocardial protection in the immature heart

Julia, P. L., Kofsky, E. R., Buckberg, G. D., Young, H., & Bugyi, H. I. (1990) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/s0022-5223(19)36831-x · Cited by 71 · see citing works

Myocardial metabolic inhibition and membrane potential, contraction, and potassium uptake

Hasin, Y., & Barry, W. H. (1984) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1984.247.2.h322 · Cited by 66 · see citing works

Pyruvate Kinase Isozymes from Rat Tissues

Osterman, J., Fritz, P. J., & Wuntch, T. (1973) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)44364-0 · Cited by 66 · see citing works

Leucine transport in Escherichia coli. The resolution of multiple transport systems and their coupling to metabolic energy.

Wood, J. M. (1975) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)41328-8 · Cited by 64 · see citing works

Developmental changes in the relation between phosphate metabolites and oxygen consumption in the sheep heart in vivo.

Portman, M. A., Heineman, F. W., & Balaban, R. S. (1989) · Journal of Clinical Investigation · doi:10.1172/jci113904 · Cited by 64 · see citing works

Metabolic oxidation of glucose during early myocardial reperfusion.

Renstrøm, B., Nellis, S. H., & Liedtke, A. J. (1989) · Circulation Research · doi:10.1161/01.res.65.4.1094 · Cited by 60 · see citing works

Transfer of fatty acids across the rabbit placenta.

Elphick, M. C., Hudson, D. G., & Hull, D. (1975) · The Journal of Physiology · doi:10.1113/jphysiol.1975.sp011132 · Cited by 60 · see citing works

Comparison of the responses of fetal and adult cardiac muscle to hypoxia

Su, J., & Wf, F. (1973) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1973.224.6.1249 · Cited by 59 · see citing works

Ultrastructural changes in rabbit heart mitochondria during the perinatal period

Smith, H. E., & Page, E. W. (1977) · Developmental Biology · doi:10.1016/0012-1606(77)90358-x · Cited by 58 · see citing works

Myocardial hibernation in the ischemic neonatal heart.

Downing, S. E., & Chen, V. (1990) · Circulation Research · doi:10.1161/01.res.66.3.763 · Cited by 57 · see citing works

Studies of myocardial protection in the immature heart. II. Evidence for importance of amino acid metabolism in tolerance to ischemia.

Julia, P. L., Young, H., Buckberg, G. D., Kofsky, E. R., & Bugyi, H. I. (1990) · PubMed · Cited by 56 · see citing works

Oxygenation and metabolism in the developing heart.

Dj, F. (1984) · PubMed · Cited by 51 · see citing works

Ventricular function and fatty acid metabolism in neonatal piglet heart

Ascuitto, R. J., Ross-Ascuitto, N. T., Chen, V., & Downing, S. E. (1989) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1989.256.1.h9 · Cited by 47 · see citing works

Studies of myocardial protection in the immature heart

Julia, P. L., Young, H., Buckberg, G. D., Kofsky, E. R., & Bugyi, H. I. (1990) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/s0022-5223(19)36832-1 · Cited by 47 · see citing works

RESPIRATORY ENZYMES IN THE HEART AND LIVER OF THE PRENATAL AND POSTNATAL RAT

Lang, C. (1965) · Biochemical Journal · doi:10.1042/bj0950365 · Cited by 46 · see citing works

Lipid burden in ischemic myocardium

Liedtke, A. (1988) · Journal of Molecular and Cellular Cardiology · doi:10.1016/0022-2828(88)90333-1 · Cited by 46 · see citing works

Palmitate transport across perfused human placenta

Szabo, A. J., Grimaldi, R. D., & Jung, W. (1969) · Metabolism · doi:10.1016/0026-0495(69)90069-9 · Cited by 45 · see citing works

Palmitate oxidation by isolated working fetal and newborn pig hearts

Werner, J. C., Sicard, R. E., & Schuler, H. G. (1989) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1989.256.2.e315 · Cited by 44 · see citing works

Increased oxidative metabolism in the fetal and newborn lamb heart

Wells, R. A., Wf, F., & Be, S. (1972) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1972.222.6.1488 · Cited by 44 · see citing works

Maturation of Energy Metabolism in the Lamb: Changes in Myosin ATPase and Creatine Kinase Activities

Ingwall, J. S., Kramer, M. F., Woodman, D., & Friedman, W. F. (1981) · Pediatric Research · doi:10.1203/00006450-198108000-00011 · Cited by 42 · see citing works

Global myocardial ischemia in the newborn, juvenile, and adult isolated isovolumic rabbit heart. Age-related differences in systolic function, diastolic stiffness, coronary resistance, myocardial oxygen consumption, and extracellular pH.

Parrish, M. D., Payne, A., & Fixler, D. E. (1987) · Circulation Research · doi:10.1161/01.res.61.5.609 · Cited by 42 · see citing works

Relationship between coronary flow and adenosine triphosphate production from glycolysis and oxidative metabolism.

Neely, J. R., Liedtke, A. J., Whitmer, J. T., & Rovetto, M. J. (1975) · PubMed · Cited by 41 · see citing works

Fatty acid and glucose utilization in isolated, working newborn pig hearts

Werner, J. C., Whitman, V., Vary, T. C., Fripp, R. R., Musselman, J., & Schuler, H. G. (1983) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1983.244.1.e19 · Cited by 40 · see citing works

Myocardial enzyme activities in guinea pigs during development

Barrie, S. E., & Harris, P. (1977) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1977.233.6.h707 · Cited by 40 · see citing works

Developmental Changes of Myocardial Metabolism

Breuer, E., Bárta, E., Zlatoš, L., & Pappová, E. (2009) · Biologia Neonatorum · doi:10.1159/000240091 · Cited by 39 · see citing works

Regulation of glycolytic flux in the heart of the fetal guinea pig.

Rolph, T., & Jones, C. T. (1983) · PubMed · Cited by 38 · see citing works

Some ultrastructural and biochemical aspects of heart mitochondria associated with development: Fetal and cardiomyopathic tissue

Sordahl, L. A. (1972) · Journal of Molecular and Cellular Cardiology · doi:10.1016/0022-2828(72)90092-2 · Cited by 36 · see citing works

A study of oogenesis and early embryogenesis in the rabbit, Oryctolagus cuniculus, with special reference to the structural changes of mitochondria

Anderson, E., Condon, W. A., & Sharp, D. C. (1970) · Journal of Morphology · doi:10.1002/jmor.1051300108 · Cited by 36 · see citing works

Ultrastructural and enzymatic development of fetal guinea pig heart

Rolph, T., Jones, C. T., & Parry, D. A. D. (1982) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1982.243.1.h87 · Cited by 35 · see citing works

Perinatal Changes in Mitochondrial Respiration of the Rabbit Heart

Werner, J. C., Whitman, V., Musselman, J., & Schuler, G. H. (2009) · Biology of the Neonate · doi:10.1159/000241601 · Cited by 33 · see citing works

The effect of dichloroacetate on the isolated no flow arrested rat heart

Burns, L. A. R., Burns, A. H., Summer, W. R., & SHEPHERD, R. E. (1989) · Life Sciences · doi:10.1016/0024-3205(89)90347-0 · Cited by 31 · see citing works

The effect of glutamate on hypoxic newborn rabbit heart

MATSUOKA, S., JARMAKANI, J. M. M., YOUNG, H., Uemura, S., & NAKANISHI, T. (1986) · Journal of Molecular and Cellular Cardiology · doi:10.1016/s0022-2828(86)80004-9 · Cited by 31 · see citing works

Developmental cardiac metabolism in health and disease

Tripp, M. E. (1989) · Pediatric Cardiology · doi:10.1007/bf02081679 · Cited by 31 · see citing works

Comparative energy metabolism in cultured heart muscle and hela cells

Stanisz, J., Wice, B. M., & Kennell, D. E. (1983) · Journal of Cellular Physiology · doi:10.1002/jcp.1041150316 · Cited by 31 · see citing works

Characterization of Glucose Metabolism in the Isolated Rat Heart During Fetal and Early Neonatal Development

Clark, C. M. (1973) · Diabetes · doi:10.2337/diab.22.1.41 · Cited by 31 · see citing works

Does the Pentose Cycle Play a Major Role for NADPH Supply in the Heart?

PFEIFER, R., Gerlinde, K. A. R. L., & Scholz, R. W. (1986) · Biological Chemistry Hoppe-Seyler · doi:10.1515/bchm3.1986.367.2.1061 · Cited by 30 · see citing works

Effect of Hypoxia on Mitochondrial Mass and Cytochrome Concentrations in Rat Heart and Liver during Postnatal Development

Kinnula, V. L., & Hassinen, I. E. (1977) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1977.tb10399.x · Cited by 28 · see citing works

Studies of myocardial protection in the immature heart

Kofsky, E. R., Julia, P. L., Buckberg, G. D., Young, H., & Tixier, D. B. (1991) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/s0022-5223(19)36791-1 · Cited by 28 · see citing works

Tissue Glycogen and Blood Glucose and Fructose Levels in the Pig Fetus during the Second Half of Gestation

Randall, G. C. B., & L'Ecuyer, C. (2009) · Biology of the Neonate · doi:10.1159/000240806 · Cited by 27 · see citing works

Relation of myocardial oxygen consumption and function to high energy phosphate utilization during graded hypoxia and reoxygenation in sheep in vivo.

Portman, M. A., Standaert, T. A., & Ning, X. H. (1995) · Journal of Clinical Investigation · doi:10.1172/jci117902 · Cited by 26 · see citing works

Glucose use in neonatal rabbit hearts reperfused after global ischemia

Itoi, T., Huang, L., & Lopaschuk, G. D. (1993) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1993.265.2.h427 · Cited by 25 · see citing works

Energy metabolism in isolated rat embryo hearts: effect of metabolic inhibitors

Cox, S. J., & Gunberg, D. L. (1972) · Development · doi:10.1242/dev.28.3.591 · Cited by 24 · see citing works

Developmental Changes of Myocardial Metabolism

Breuer, E., Barta, E., Pappová, E., & Zlatoš, L. (2009) · Biologia Neonatorum · doi:10.1159/000240080 · Cited by 23 · see citing works

Development and Adaptation of Heart Mitochondrial Respiratory Chain Function in Fetus and in Newborn

Goodwin, C. W., Mela, L., DEUTSCH, C. J., Forster, R. E., Miller, L. D., & Delivoria‐Papadopoulos, M. (1976) · Advances in experimental medicine and biology · doi:10.1007/978-1-4684-3273-2_83 · Cited by 22 · see citing works

CTYOCHROME C CONCENTRATIONS DURING RAT AND GUINEA PIG DEVELOPMENT.

Dallman, P. R., & Schwartz, H. C. (1964) · PubMed · Cited by 21 · see citing works

Carbohydrate metabolism in isolated, working newborn pig heart

Werner, J. C., Whitman, V., Fripp, R. R., Schuler, H. G., & Morgan, H. E. (1981) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1981.241.5.e364 · Cited by 21 · see citing works

CYTOCHROME c CONCENTRATIONS DURING RAT AND GUINEA PIG DEVELOPMENT

Dallman, P. R., & Schwartz, H. C. (1964) · PEDIATRICS · doi:10.1542/peds.33.1.106 · Cited by 21 · see citing works

Carnitine palymityltransferase in neonatal and adult heart and liver mitochondria. Effect of phospholipase C treatment.

Wood, J. M. (1975) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)41594-9 · Cited by 20 · see citing works

Metabolic and functional responses of immature and mature rabbit hearts to hypoperfusion, ischemia, and reperfusion

Matherne, G. P., Headrick, J. P., Berr, S. S., & Berne, R. M. (1993) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1993.264.6.h2141 · Cited by 19 · see citing works

Oxygen uptake during early cardiogenesis of the chick

Raddatz, E., Servin, M., & Kučera, P. (1992) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1992.262.4.h1224 · Cited by 18 · see citing works

Fatty acid and glucose utilization in isolated, working fetal pig hearts

Werner, J. C., Whitman, V., Fripp, R. R., Schuler, H. G., Musselman, J., & Sham, R. L. (1983) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1983.245.1.e19 · Cited by 18 · see citing works

LEUCINE TRANSPORT IN ESCHERICHIA COLI

Oxender, D. L., & Rahmanian, M. (1972) · Elsevier eBooks · doi:10.1016/b978-0-12-761250-8.50016-1 · Cited by 17 · see citing works

Multiple forms of phosphofructokinase in developing rabbit and guinea pig tissues

de Faria, J. B., El-Dorry, H. A., & Bacila, M. (1978) · Developmental Biology · doi:10.1016/0012-1606(78)90051-9 · Cited by 13 · see citing works

Metabolic consequences of anoxia in the isolated, perfused guinea pig heart: Anaerobic metabolism of endogenous amino acids

Brainard, J. R., Hoekenga, D. E., & Hutson, J. Y. (1986) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910030504 · Cited by 13 · see citing works

Development of Enzymes of Energy Metabolism in Rat Heart

Andrés, A., Satrústegui, J., & Machado, A. (2009) · Biology of the Neonate · doi:10.1159/000241780 · Cited by 13 · see citing works

Myocardial Energy Metabolism in the Newborn Lamb In Vivo during Pacing-Induced Changes in Oxygen Consumption

Portman, M. A., & Ning, X.-H. (1995) · Pediatric Research · doi:10.1203/00006450-199502000-00010 · Cited by 11 · see citing works

Wall tension and myocardial dysfunction after ischemia and reperfusion

Downing, S. E. (1993) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1993.264.2.h386 · Cited by 10 · see citing works

Mechanical function and fatty acid oxidation in the neonatal pig heart with ischemia and reperfusion.

Ascuitto, R. J., Ross-Ascuitto, N. T., Ramage, D., & McDonough, K. H. (1990) · PubMed · Cited by 10 · see citing works

Myocardial buffering capacity and high-energy phosphate utilization during hypothermic circulatory arrest and recovery in the newborn lamb in vivo

Portman, M. A., & Eyster, G. E. (1994) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/s0022-5223(94)70195-4 · Cited by 9 · see citing works

Plaque Reduction, a Sensitive Test for Eastern Encephalitis Antibody

Daniels, J. B., Ratner, J. J., & Brown, S. R. (1961) · Science · doi:10.1126/science.133.3453.640 · Cited by 8 · see citing works

Mechanical and Metabolic Characterization of Ischemic Contracture in the Neonatal Pig Heart

Ascuitto, R. J., Ross-Ascuitto, N. T., Kydon, D. W., Waddell, A. E., & McDonough, K. H. (1995) · Pediatric Research · doi:10.1203/00006450-199508000-00016 · Cited by 8 · see citing works

Altered Maternal Thyroid Function: Fetal and Neonatal Myocardial Metabolism

Kumar, R., & Chaudhuri, B. (2009) · Biology of the Neonate · doi:10.1159/000243205 · Cited by 7 · see citing works

Glucose, Acetate, and Lactate Metabolism in Perirenal Adipose Tissue of Fetal and Newborn Calves

Wijayasinghe, M. S. (1986) · Pediatric Research · doi:10.1203/00006450-198606000-00012 · Cited by 5 · see citing works

Force and Oxygen Consumption in the Immature Rabbit Heart

Parrish, M. D., & Farrar, S. (1990) · Pediatric Research · doi:10.1203/00006450-199005000-00012 · Cited by 5 · see citing works

Maturation of Energy Metabolism in the Lamb

Ingwall, J. S., Kramer, M. F., Woodman, D. A., & Friedman, W. F. (1981) · Pediatric Research · doi:10.1203/00006450-198115080-00011 · Cited by 5 · see citing works

OXIDATIVE METABOLISM IN NEONATAL PIG HEARTS STRESSED WITH PACING-INDUCED TACHYCARDIA. • 114

Ascuitto, R. J., Ross-Ascuitto, N. T., & Waddell, A. E. (1996) · Pediatric Research · doi:10.1203/00006450-199604001-00133 · Cited by 1 · see citing works

GLUCOSE METABOLISM IN NEONATAL PIG HEARTS SUBJECTED TO HYPOXIA FOLLOWED BY REOXYGENATION. † 198

Ross-Ascuitto, N. T., Ascuitto, R. J., & Waddell, A. E. (1996) · Pediatric Research · doi:10.1203/00006450-199604001-00217 · Cited by 1 · see citing works

Hypoxia and Fetal Heart Development

Patterson, A. J., & Zhang, L. (2010) · Current Molecular Medicine · doi:10.2174/156652410792630643 · Cited by 240 · see citing works

Maturation of Cardiac Energy Metabolism During Perinatal Development

Piquereau, J., & Ventura‐Clapier, R. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00959 · Cited by 213 · see citing works

Developmental toxicity of nicotine: A transdisciplinary synthesis and implications for emerging tobacco products

England, L. J., Aagaard, K., Bloch, M., Conway, K., Cosgrove, K., Grana, R., Gould, T. J., Hatsukami, D., Jensen, F., Kandel, D., et al. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.11.013 · Cited by 181 · see citing works

Myocardial VHL-HIF Signaling Controls an Embryonic Metabolic Switch Essential for Cardiac Maturation

Menendez-Montes, I., Escobar, B., Palacios, B., Gómez, M. J., Izquierdo-García, J. L., Flores, L., Jiménez‐Borreguero, L. J., Aragonés, J., Ruı́z-Cabello, J., Torres, M., et al. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.11.012 · Cited by 144 · see citing works

HIF-1, Metabolism, and Diabetes in the Embryonic and Adult Heart

Čerychová, R., & Pavlínková, G. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00460 · Cited by 142 · see citing works

Three‐Dimensional Paper‐Based Model for Cardiac Ischemia

Mosadegh, B., Dabiri, B. E., Lockett, M. R., Derda, R., Campbell, P. H., Parker, K. K., & Whitesides, G. M. (2014) · Advanced Healthcare Materials · doi:10.1002/adhm.201300575 · Cited by 134 · see citing works

Adaptation to myocardial stress in disease states: is preconditioning a healthy heart phenomenon?

Ferdinandy, P., Szilvássy, Z., & Baxter, G. F. (1998) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(98)01212-7 · Cited by 118 · see citing works

PPARdelta activation induces metabolic and contractile maturation of human pluripotent stem cell-derived cardiomyocytes

Wickramasinghe, N. M., Sachs, D. M., Shewale, B., Gonzalez, D. M., Dhanan-Krishnan, P., Torre, D., LaMarca, E. A., Raimo, S., Dariolli, R., Serasinghe, M. N., et al. (2022) · Cell stem cell · doi:10.1016/j.stem.2022.02.011 · Cited by 99 · see citing works

Cardiac hypertrophy in mice with long-chain acyl-CoA dehydrogenase or very long-chain acyl-CoA dehydrogenase deficiency

Cox, K. B., Liu, J., Tian, L., Barnes, S., Yang, Q., & Wood, P. A. (2009) · Laboratory Investigation · doi:10.1038/labinvest.2009.86 · Cited by 66 · see citing works

Palmitate-induced cardiac apoptosis is mediated through CPT-1 but not influenced by glucose and insulin

Kong, J. Y., & Rabkin, S. W. (2002) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00257.2001 · Cited by 61 · see citing works

Cardiomyocyte cell cycling, maturation, and growth by multinucleation in postnatal swine

Velayutham, N., Alfieri, C. M., Agnew, E. J., Riggs, K. W., Baker, R. S., Ponny, S. R., Zafar, F., & Yutzey, K. E. (2020) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2020.07.004 · Cited by 63 · see citing works

Cellular effects and clinical implications of SLC2A3 copy number variation

Ziegler, G. C., Álmos, P. Z., McNeill, R. V., Jansch, C., & Lesch, K. (2020) · Journal of Cellular Physiology · doi:10.1002/jcp.29753 · Cited by 57 · see citing works

Transcriptional Regulation of Postnatal Cardiomyocyte Maturation and Regeneration

Padula, S. L., Velayutham, N., & Yutzey, K. E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22063288 · Cited by 52 · see citing works

Initiation of Electron Transport Chain Activity in the Embryonic Heart Coincides with the Activation of Mitochondrial Complex 1 and the Formation of Supercomplexes

Beutner, G., Eliseev, R. A., & Porter, G. A., Jr. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113330 · Cited by 51 · see citing works

Postnatal Cardiac Development and Regenerative Potential in Large Mammals

Velayutham, N., Agnew, E. J., & Yutzey, K. E. (2019) · Pediatric Cardiology · doi:10.1007/s00246-019-02163-7 · Cited by 51 · see citing works

Diagnosis and Management of Fetal Heart Failure

Thakur, V., Fouron, J., Mertens, L., & JAEGGI, E. T. (2013) · Canadian Journal of Cardiology · doi:10.1016/j.cjca.2013.02.001 · Cited by 49 · see citing works

Modelling ischemia-reperfusion injury (IRI) in vitro using metabolically matured induced pluripotent stem cell-derived cardiomyocytes

Hidalgo, A., Glass, N. R., Ovchinnikov, D. A., Yang, S., Zhang, X., Mazzone, S. B., Chen, C., Wolvetang, E. J., & Cooper-White, J. J. (2018) · APL Bioengineering · doi:10.1063/1.5000746 · Cited by 46 · see citing works

Formation of highly organized intracellular structure and energy metabolism in cardiac muscle cells during postnatal development of rat heart

Anmann, T., Varikmaa, M., Timohhina, N., Tepp, K., Shevchuk, I. N., Chekulayev, V. A., Saks, V. A., & Käämbre, T. (2014) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2014.03.015 · Cited by 45 · see citing works

Metabolic Determinants of Cardiomyocyte Proliferation

Mohamed, T., Abouleisa, R., & Hill, B. G. (2022) · Stem Cells · doi:10.1093/stmcls/sxac016 · Cited by 41 · see citing works

Cardiomyocyte Proliferation from Fetal- to Adult- and from Normal- to Hypertrophy and Failing Hearts

Bishop, S. P., Zhang, J. J., & Ye, L. (2022) · Biology · doi:10.3390/biology11060880 · Cited by 45 · see citing works

A change of heart: understanding the mechanisms regulating cardiac proliferation and metabolism before and after birth

Dimasi, C. G., Darby, J. R. T., & Morrison, J. L. (2023) · The Journal of Physiology · doi:10.1113/jp284137 · Cited by 40 · see citing works

Proliferation and Maturation: Janus and the Art of Cardiac Tissue Engineering

Singh, B. N., Yücel, D., Garay, B. I., Tolkacheva, E. G., Kyba, M., Perlingeiro, R. C. R., van Berlo, J. H., & Ogle, B. M. (2023) · Circulation Research · doi:10.1161/circresaha.122.321770 · Cited by 39 · see citing works

Metabolic Maturation Increases Susceptibility to Hypoxia-induced Damage in Human iPSC-derived Cardiomyocytes

Peters, M. M. C., Maas, R. G. C., van Adrichem, I., Doevendans, P. A., Mercola, M. A., Šarić, T., Buikema, J. W., van Mil, A., Chamuleau, S. A. J., Sluijter, J. P. G., et al. (2022) · Stem Cells Translational Medicine · doi:10.1093/stcltm/szac061 · Cited by 38 · see citing works

Limitations and vulnerabilities of the neonatal cardiovascular system: considerations for anesthetic management

WOLF, A. R., & Humphry, A. (2013) · Pediatric Anesthesia · doi:10.1111/pan.12290 · Cited by 35 · see citing works

Reactive oxygen at the heart of metabolism

Murray, T. V., Ahmad, A. N., & Brewer, A. C. (2013) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2013.09.003 · Cited by 26 · see citing works

Fetal Programming and Sexual Dimorphism of Mitochondrial Protein Expression and Activity of Hearts of Prenatally Hypoxic Guinea Pig Offspring

Thompson, L. P., Song, H., & Polster, B. M. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/7210249 · Cited by 23 · see citing works

Metabolic Efficiency Promotes Protection From Pressure Overload in Hearts Expressing Slow Skeletal Troponin I

Carley, A. N., Taglieri, D. M., Bi, J., Solaro, R. J., & Lewandowski, E. D. (2014) · Circulation Heart Failure · doi:10.1161/circheartfailure.114.001496 · Cited by 22 · see citing works

Metabolic environment in vivo as a blueprint for differentiation and maturation of human stem cell-derived cardiomyocytes

Slaats, R. H., Schwach, V., & Passier, R. C. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2020.165881 · Cited by 21 · see citing works

Newborn hearts are at greater ‘metabolic risk’ during global ischemia – advantages of continuous coronary washout

Wittnich, C., Belanger, M. P., & Bandali, K. S. (2007) · Canadian Journal of Cardiology · doi:10.1016/s0828-282x(07)70743-2 · Cited by 21 · see citing works

Effects of Chronic Hypoxia on Fetal Coronary Responses

Thompson, L. P. (2003) · High Altitude Medicine & Biology · doi:10.1089/152702903322022811 · Cited by 21 · see citing works

Remote ischemic preconditioning impairs ventricular function and increases infarct size after prolonged ischemia in the isolated neonatal rabbit heart

Schmidt, M. R., Støttrup, N. B., Michelsen, M. M., Contractor, H., Sørensen, K. E., Kharbanda, R. K., Redington, A. N., & Bøtker, H. E. (2013) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/j.jtcvs.2013.05.022 · Cited by 19 · see citing works

Redox ratio in the left ventricle of the growth restricted fetus is positively correlated with cardiac output

Dimasi, C. G., Łaźniewska, J., Plush, S. E., Saini, B. S., Holman, S. L., Cho, S. K. S., Wiese, M. D., Sorvina, A., Macgowan, C. K., Seed, M., et al. (2021) · Journal of Biophotonics · doi:10.1002/jbio.202100157 · Cited by 19 · see citing works

Glucose-insulin infusion improves cardiac function during fetal tachycardia

Schmidt, M. R., Kristiansen, S. B., White, P. A., Smerup, M., Bøtker, H. E., Vogel, M., Hjortdal, V. E., Sørensen, K. E., & Redington, A. N. (2004) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2003.08.041 · Cited by 19 · see citing works

Expression of slow skeletal TnI in adult mouse hearts confers metabolic protection to ischemia

Pound, K. M., Arteaga, G. M., Fasano, M., Wilder, T., Fischer, S. K., Warren, C. M., Wende, A. R., Farjah, M., Abel, E. D., Solaro, R. J., et al. (2011) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2011.05.014 · Cited by 19 · see citing works

Energy metabolism homeostasis in cardiovascular diseases.

Wang, L.-Y., & Chen, C. (2021) · PubMed Central · doi:10.11909/j.issn.1671-5411.2021.12.006 · Cited by 18 · see citing works

Developmental determinants of cardiac sensitivity to hypoxia

Ostadal, B., Ostadalova, I., Kolář, F., & Sedmera, D. (2014) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2013-0498 · Cited by 17 · see citing works

Cardiomyocyte Ploidy, Metabolic Reprogramming and Heart Repair

Elia, A., Mohsin, S., & Khan, M. (2023) · Cells · doi:10.3390/cells12121571 · Cited by 15 · see citing works

Single-cell multi-modal integrative analyses highlight functional dynamic gene regulatory networks directing human cardiac development

Holman, A. R., Tran, S., Destici, E., Farah, E. N., Li, T., Nelson, A. C., Engler, A. J., & Neil, C. (2024) · Cell Genomics · doi:10.1016/j.xgen.2024.100680 · Cited by 16 · see citing works

Validation of 99mTc-labeled “4+1” fatty acids for myocardial metabolism and flow imaging

Mirtschink, P., Stehr, S. N., Walther, M., Pietzsch, J., Bergmann, R., Pietzsch, H., Weichsel, J., Pexa, A., Dieterich, P., Wunderlich, G., et al. (2009) · Nuclear Medicine and Biology · doi:10.1016/j.nucmedbio.2009.06.009 · Cited by 14 · see citing works

Increased fetal myocardial sensitivity to insulin-stimulated glucose metabolism during ovine fetal growth restriction

Barry, J. S., Rozance, P. J., Brown, L. D., Anthony, R. V., Thornburg, K. L. R., & Hay, W. W. (2016) · Experimental Biology and Medicine · doi:10.1177/1535370216632621 · Cited by 14 · see citing works

Maturation of lipid metabolism in the fetal and newborn sheep heart

Drake, R., Louey, S., & Thornburg, K. L. R. (2023) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00122.2023 · Cited by 13 · see citing works

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

Chang, E. I., Stremming, J., Knaub, L. A., Wesolowski, S. R., Rozance, P. J., Sucharov, C. C., Reusch, J. E. B., & Brown, L. D. (2024) · The Journal of Physiology · doi:10.1113/jp285496 · Cited by 13 · see citing works

Validation of 99mTc-labeled “4+1” fatty acids for myocardial metabolism and flow imaging

Mirtschink, P., Stehr, S. N., Walther, M., Pietzsch, J., Bergmann, R., Pietzsch, H., Weichsel, J., Pexa, A., Dieterich, P., Wunderlich, G., et al. (2009) · Nuclear Medicine and Biology · doi:10.1016/j.nucmedbio.2009.06.003 · Cited by 12 · see citing works

GATAD1 is involved in sphingosylphosphorylcholine-attenuated myocardial ischemia-reperfusion injury by modulating myocardial fatty acid oxidation and glucose oxidation

Cai, Y., Yu, Y., Zhang, T., Qian, B., Wang, B., Yan, W., & Zhao, J. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.11.054 · Cited by 11 · see citing works

Electrocardiographic changes following umbilical cord occlusion in the midgestation fetal sheep

Welin, A.-K., Blad, S., Hagberg, H., Rosén, K. G., Kjellmer, I., & Mallard, C. E. (2005) · Acta Obstetricia Et Gynecologica Scandinavica · doi:10.1080/j.0001-6349.2005.00594.x · Cited by 11 · see citing works

The role of metabolism in cardiac development

Nakano, H., & Nakano, A. (2024) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2024.01.005 · Cited by 10 · see citing works

Values of T/QRS ratio in pregnancies complicated by intrauterine growth restriction

Fuchs, T. (2016) · Journal of Perinatal Medicine · doi:10.1515/jpm-2014-0305 · Cited by 10 · see citing works

Mechanical Function and Substrate Oxidation in the Neonatal Pig Heart Subjected to Pacing-Induced Tachycardia

Ascuitto, R. J., Joyce, J. J., & Ross-Ascuitto, N. T. (1999) · Molecular Genetics and Metabolism · doi:10.1006/mgme.1998.2791 · Cited by 10 · see citing works

Cardiac Metabolism in the Fetus and Newborn

SCHOLZ, T. D., & Segar, J. L. (2008) · NeoReviews · doi:10.1542/neo.9-3-e109 · Cited by 9 · see citing works

Comparative Metabolomics in Single Ventricle Patients after Fontan Palliation: A Strong Case for a Targeted Metabolic Therapy

Renaud, D., Scholl‐Bürgi, S., Karall, D., & Michel, M. (2023) · Metabolites · doi:10.3390/metabo13080932 · Cited by 8 · see citing works

Integrated small RNA, mRNA and protein omics reveal a miRNA network orchestrating metabolic maturation of the developing human heart

Aharon-Yariv, A., Wang, Y., Ahmed, A., & Delgado-Olguı́n, P. (2023) · BMC Genomics · doi:10.1186/s12864-023-09801-8 · Cited by 7 · see citing works

Does cardiac development provide heart research with novel therapeutic approaches?

Sayed, A., Valente, M., & Sassoon, D. A. (2018) · F1000Research · doi:10.12688/f1000research.15609.1 · Cited by 8 · see citing works

Values of T/QRS ratios measured during normal and post-term pregnancies

Fuchs, T. (2013) · Journal of Perinatal Medicine · doi:10.1515/jpm-2013-0181 · Cited by 7 · see citing works

Heme oxygenase/carbon monoxide system and development of the heart

Mahan, V. L. (2024) · Medical Gas Research · doi:10.4103/mgr.medgasres-d-24-00031 · Cited by 6 · see citing works

Transition to extrauterine life and the modeling of perinatal asphyxia in rats

Ortiz, M., Loidl, C. F., & Vázquez‐Borsetti, P. (2022) · WIREs Mechanisms of Disease · doi:10.1002/wsbm.1568 · Cited by 6 · see citing works

Cardiac Metabolic Adaptation During Postnatal Development

Piquereau, J., Novotová, M., Garnier, A., Joubert, F., Veksler, V., & Ventura‐Clapier, R. (2012) · Springer eBooks · doi:10.1007/978-1-4614-5203-4_5 · Cited by 6 · see citing works

Effects of prenatal hypoxia on fetal sheep heart development and proteomics analysis.

Li, H., Hu, J., Liu, Y., Wang, X., Tang, S., Chen, X., Niu, M., Waili, N., Bai, Y., & Wei, Y. (2018) · PubMed Central · Cited by 6 · see citing works

Cardiac growth patterns and metabolism before and after birth in swine: Role of miR in proliferation, hypertrophy and metabolism

Dimasi, C. G., Darby, J. R. T., Holman, S. L., Quinn, M., Meakin, A. S., Seed, M., Wiese, M. D., & Morrison, J. L. (2024) · Journal of Molecular and Cellular Cardiology Plus · doi:10.1016/j.jmccpl.2024.100084 · Cited by 5 · see citing works

Energy Metabolism in Cardiomyocyte

Kartha, C. C. (2021) · Springer eBooks · doi:10.1007/978-3-030-85536-9_7 · Cited by 5 · see citing works

Cardiotin localization in mitochondria of cardiomyocytes in vivo and in vitro and its down-regulation during dedifferentiation

Driesen, R. B., Verheyen, F., Schaart, G., Mazière, A. M. G. L. D., Viebahn, C., Prinzen, F. W., Lenders, M. ‐., Debie, W. M. H., Totzeck, A., Borgers, M. J., et al. (2008) · Cardiovascular Pathology · doi:10.1016/j.carpath.2007.12.008 · Cited by 5 · see citing works

Engineering Smart Biomaterial Interfaces for iPSC-CM Maturation: A Biophysical and Metabolic Reprogramming Approach to Regenerative Cardiac Medicine

Shahannaz, D. C., & Sugiura, T. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27062637 · Cited by 4 · see citing works

Histological changes in the bullfrog (Lithobates catesbeianus) myocardium induced by severe hypoxia during embryonic development

Lima, I. B., Silva, N. G. D., Machado, J. R., Machado, J. F. F., & Rivaroli, L. (2021) · Biologia · doi:10.2478/s11756-020-00656-y · Cited by 4 · see citing works

Cardiomyocyte maturation and proliferation is a flip coin

Abouleisa, R., Farraj, K. A., Mehta, S., & Mohamed, T. (2025) · BMC Cardiovascular Disorders · doi:10.1186/s12872-025-05360-w · Cited by 2 · see citing works

Hemodynamic Adaptation to Hypoxia in Neonatal Critical Care

van Elteren, H. A., İnce, C., & Reiss, I. K. M. (2013) · Springer eBooks · doi:10.1007/978-3-642-35109-9_17 · Cited by 2 · see citing works

Age-related issues: From fetus to adolescent

Favilli, S., Prandstraller, D., Spaziani, G., Calabri, G. B., Lombardi, M., Balducci, A., & Vairo, U. (2018) · Progress in Pediatric Cardiology · doi:10.1016/j.ppedcard.2018.08.003 · Cited by 2 · see citing works

Performance of the Neonatal Pig Heart Subjected to Oxygen Insufficiency

Uy, R., Tede, N. H., Ross-Ascuitto, N. T., & Ascuitto, R. J. (2003) · Neonatology · doi:10.1159/000074957 · Cited by 2 · see citing works

Seahorse Metabolic Analysis for Human and Mouse Cardiac Organotypic SlicesPreprint

Trampel, K. A., Li, B., Melisova, A., Madrid, M. K., George, S. A., & Efimov, I. R. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.11.659150 · Cited by 2 · see citing works

In silico studies of energy metabolism of normal and diseased heart

Ngai, S. M., Way, M. M. Y., Chan, H., Tsui, S. K., Lee, C. Y., & Fung, K. (2000) · Molecular Biology Reports · doi:10.1023/a:1007121822920 · Cited by 2 · see citing works

Enhancing Cardiomyocyte Purity through Lactate-Based Metabolic Selection

Seo, S. J., & Jin, Y. (2025) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-024-00696-4 · Cited by 1 · see citing works

Effects of High Glucose on Simulated Ischemia/Reperfusion Injury in Isolated Cardiomyocytes

Walter, M. J. K., Shiota, M., Li, Z., Barajas, M. B., Oyama, T., & Riess, M. L. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26136050 · Cited by 1 · see citing works

Ischaemia and Infarction

Ashworth, M. T. (2019) · Cambridge University Press eBooks · doi:10.1017/9781316337073.006 · Cited by 1 · see citing works

PPARdelta signaling activation improves metabolic and contractile maturation of human pluripotent stem cell-derived cardiomyocytesPreprint

Wickramasinghe, N. M., Sachs, D. M., Shewale, B., Gonzalez, D. M., Dhanan-Krishnan, P., Torre, D., LaMarca, E. A., Raimo, S., Dariolli, R., Serasinghe, M. N., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.12.451352 · Cited by 1 · see citing works

Doppler Ultrasound Examination of the Fetal Coronary Circulation

Baschat, A. (2005) · Springer eBooks · doi:10.1007/3-540-28903-8_29

Altered maternal thyroid function: Effect of L-carnitine supplementation on fetal and neonatal myocardial free fatty acid oxidation,in vitro

Kumar, R. (1998) · Indian Journal of Clinical Biochemistry · doi:10.1007/bf02867868

Implications of a Low-Carbohydrate, High-Fat Diet on Heart Size in a Murine Model

Gresty, K. M., Scheede‐Bergdahl, C., & Bergdahl, A. (2014) · International Journal of Cardiovascular and Cerebrovascular Disease · doi:10.13189/ijccd.2014.020301

Critically Ill Children and the Microcirculation: Go with the Flow?

Buijs, E. A. B. (2014) · EUR Research Repository (Erasmus University Rotterdam)

Improved Cardiac Glucose Uptake: A Potential Mechanism for Estrogens to Prevent the Development of Cardiac Hypertrophy

Würzburg, J.-M.-U. (2009)

Ventilación y lactato sanguíneo en niños durante una prueba máxima incremental en cicloergómetro

Jiménez, I. V., Cordero, M. J. A., Barrilao, R. G., Orellana, J. N., & Almeida, L. G. (2016) · Nutrición Hospitalaria · doi:10.20960/nh.132

The Neonatal Transition of the Right Ventricle

Maria, M. V. D., & Abman, S. H. (2014) · Respiratory medicine · doi:10.1007/978-1-4939-1065-6_3

Métabolisme énergétique cardiaque fœtal dans un modèle de restriction de croissance intra-utérine chez le rat

Monfils, S. (2011) · doi:10.71781/29584

Cardiac Metabolism During Development and Aging

Schrepper, A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-802394-5.00006-6

Ultrasound examination of the fetal coronary circulation

Baschat, A., & Gembruch, U. (2008) · Series in maternal-fetal medicine · doi:10.3109/9781439807989.027

Chronic Hypoxia Induces Epigenetic Modifications in the Fetal Rat Heart

Patterson, A. J. (2011) · The Scholars Repository - LLU (Loma Linda University)

Cardiac Metabolic Protection for the Newborn Heart

Ralphe, J. C., & SCHOLZ, T. D. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1227-8_17

Simultaneous activation of PKA and Epac is cardioprotective in neonatal and adult hearts

Lewis, M. (2019) · Bristol Research (University of Bristol)

Modelling the human heart: human stem cell-based models lead the way in physiological, pathological, and toxicological research

Slaats, R. H. (2021) · doi:10.3990/1.9789036552318

Adaptive remodeling of cardiomyocytes under stress

Driesen, R. B. (2008) · doi:10.26481/dis.20080320rd

PW1/Peg3+ cells respond to hypoxia in the adult heart

Sayed, A. (2019) · theses.fr (ABES) · doi:10.70675/722787a3z5efbz4ed9zadfaz56c6f7fc4045

Hypoxia: the acid test for the neonatal heart!?

Binkhorst, M., & Hogeveen, M. (2026) · Resuscitation · doi:10.1016/j.resuscitation.2026.111255

Molekulare Ursachen myokardialer Insuffizienz beim Neugeborenen

Kreuder, J. G., & Schranz, D. (2005) · Springer eBooks · doi:10.1007/3-540-26524-4_20

Cardiac Metabolism During Development and Aging

Schrepper, A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-802394-5.00006-6

Developmental changes in energy substrate use by the heart

Lopaschuk, G. D., Collins-Nakai, R. L., & Itoi, T. (1992) · Cardiovascular Research · doi:10.1093/cvr/26.12.1172 · Cited by 325 · see citing works

Regulation of Cardiac Energy Metabolism in Newborn

Onay-Beşi̇kçi̇, A. (2006) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-006-9123-9 · Cited by 58 · see citing works

Maturation of fatty acid and carbohydrate metabolism in the newborn heart

Makinde, A.-O., Kantor, P. F., & Lopaschuk, G. D. (1998) · Molecular and Cellular Biochemistry · doi:10.1023/a:1006860104840 · Cited by 114 · see citing works

Developmental cardiac metabolism in health and disease

Tripp, M. E. (1989) · Pediatric Cardiology · doi:10.1007/bf02081679 · Cited by 31 · see citing works