AbstractObjectiveGlucose is an important substrate for energy production in the developing heart. Increased glucose uptake rate and metabolism during ischemia and reperfusion are closely linked to postischemic myocardial recovery. The initial rate-limiting step for glycolysis is the transport of glucose across the plasma membrane by glucose transporters (GLUT-1 and GLUT-4). We hypothesized that changes in GLUT-1 and GLUT-4 expression in developing hearts lead to age-dependent adaptive changes in glucose uptake capacity and influence tolerance to ischemia.MethodsWestern-immunoblotting was performed to determine GLUT-1 and GLUT-4 expression in myocardial tissue from 1, 2, and 3-week-old and adult rabbits. Glucose uptake rate was measured with...
Cardiac hypertrophy may be associated with an enhanced susceptibility to ischaemic/reperfusion injur...
Induced pluripotent stem cell derived cardiomyocytes (iPSC-CM) have the potential to transform regen...
Background-—Increased glucose transporter 1 (GLUT1) expression and glucose utilization that accompan...
AbstractObjectiveGlucose is an important substrate for energy production in the developing heart. In...
The mammalian heart switches its main metabolic substrate from glucose to fatty acids shortly after ...
Glucose constitutes a major fuel for the heart, and high glucose uptake during fetal development is ...
AbstractThe ability of the heart muscle to derive energy from a wide variety of substrates provides ...
Pre-diabetic subjects with high insulin secretory capacity have double risk of cardiovascular diseas...
We determined that there were no regional differences in GLUT1 or GLUT4 expression in normal dog hea...
We recently observed that glycogen loading of the heart in vivo improves ischemia tolerance to the s...
Impaired glucose uptake is associated with both cardiac hypertrophy and contractile dysfunction, but...
AbstractObjectiveHyperglycemia has been found to occur in children placed on cardiopulmonary bypass....
The efficacy of increasing glycolysis during ischemia for enhancing the salutary effects of reperfus...
Objective: In vivo differentiation of cardiac myocytes is associated with downregulation of the gluc...
AbstractObjectivesWe sought to evaluate the time course of insulin-stimulated myocardial glucose upt...
Cardiac hypertrophy may be associated with an enhanced susceptibility to ischaemic/reperfusion injur...
Induced pluripotent stem cell derived cardiomyocytes (iPSC-CM) have the potential to transform regen...
Background-—Increased glucose transporter 1 (GLUT1) expression and glucose utilization that accompan...
AbstractObjectiveGlucose is an important substrate for energy production in the developing heart. In...
The mammalian heart switches its main metabolic substrate from glucose to fatty acids shortly after ...
Glucose constitutes a major fuel for the heart, and high glucose uptake during fetal development is ...
AbstractThe ability of the heart muscle to derive energy from a wide variety of substrates provides ...
Pre-diabetic subjects with high insulin secretory capacity have double risk of cardiovascular diseas...
We determined that there were no regional differences in GLUT1 or GLUT4 expression in normal dog hea...
We recently observed that glycogen loading of the heart in vivo improves ischemia tolerance to the s...
Impaired glucose uptake is associated with both cardiac hypertrophy and contractile dysfunction, but...
AbstractObjectiveHyperglycemia has been found to occur in children placed on cardiopulmonary bypass....
The efficacy of increasing glycolysis during ischemia for enhancing the salutary effects of reperfus...
Objective: In vivo differentiation of cardiac myocytes is associated with downregulation of the gluc...
AbstractObjectivesWe sought to evaluate the time course of insulin-stimulated myocardial glucose upt...
Cardiac hypertrophy may be associated with an enhanced susceptibility to ischaemic/reperfusion injur...
Induced pluripotent stem cell derived cardiomyocytes (iPSC-CM) have the potential to transform regen...
Background-—Increased glucose transporter 1 (GLUT1) expression and glucose utilization that accompan...