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1.
J Mol Cell Cardiol ; 31(5): 1143-55, 1999 May.
Artigo em Inglês | MEDLINE | ID: mdl-10336852

RESUMO

A number of observations indicate that myocardial glucose utilization is increased late during post-ischemic reperfusion. The present study was designed to examine whether transient ischemia elicits altered expression of glucose transporters GLUT-1 and GLUT-4. In rats, the left anterior descending coronary artery was occluded for 20 min followed by reperfusion for 1, 3 or 7 days. Regional myocardial uptake and phosphorylation of glucose was determined based on myocardial accumulation of 2-deoxy-D-[2, 6-3H]glucose-6-phosphate. In hearts from fasted rats, after 3 days of reperfusion, myocardial uptake and phosphorylation of glucose was 48% higher in the reperfused region compared to a remote control region. No regional difference in myocardial glucose uptake and phosphorylation was detectable in hearts from fed rats. After 1 day of reperfusion, expression of myocardial glucose transporter GLUT-1 mRNA was increased to 195+/-24% (mean+/-SEM) of the value measured in the remote region and the expression of GLUT-4 mRNA was decreased to 58+/-7%. After 3 days of reperfusion both mRNA and protein of GLUT-1 were higher in the reperfused region, averaging 133+/-23% and 249+/-36%, respectively. The corresponding values for GLUT-4 mRNA and protein were 77+/-7% and 62+/-6%, respectively. The results indicate that a short period of ischemia alters the expression of glucose transporter isoforms GLUT-1 and GLUT-4. Observed changes may be involved in the mechanisms underlying late changes of substrate metabolism during reperfusion.


Assuntos
Proteínas de Transporte de Monossacarídeos/metabolismo , Proteínas Musculares , Isquemia Miocárdica/metabolismo , Doença Aguda , Animais , Fator Natriurético Atrial/metabolismo , Glicemia/metabolismo , Desoxiglucose/metabolismo , Ácidos Graxos/sangue , Código Genético , Transportador de Glucose Tipo 1 , Transportador de Glucose Tipo 4 , Insulina/sangue , Masculino , Reperfusão Miocárdica , Fosforilação , RNA Mensageiro/biossíntese , Ratos , Ratos Wistar
2.
J Mol Cell Cardiol ; 30(2): 393-403, 1998 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-9515016

RESUMO

Myocardial ischemia elicits translocation of the insulin-sensitive glucose transporter GLUT-4 from intracellular membrane stores to the sarcolemma. Because glucose metabolism is of crucial importance for post-ischemic recovery of the heart, myocardial uptake of [3H]-labeled 2-deoxyglucose and subcellular localization of GLUT-4 were determined during reperfusion in isolated rat hearts perfused with medium containing 0.4 mm palmitate and 8 mm glucose. Hearts were subjected to 20 min of no-flow ischemia, followed by reperfusion for up to 60 min. Subcellular localization of GLUT-4 was determined by cell fractionation followed by immunoblotting. After 15 and 60 min of reperfusion uptake of 2-deoxyglucose was significantly higher (91+/-9 and 96+/-8 nmol/min/g wet weight, respectively) as compared to control values (65+/-1 nmol/min/g wet weight). Ischemia elicited translocation of GLUT-4 to the sarcolemma, which persisted after 15 min of reperfusion. However, after 60 min of reperfusion the subcellular distribution of GLUT-4 was similar to control hearts. In conclusion, reversal of ischemia-induced translocation of GLUT-4 to the sarcolemma is rather slow, possibly facilitating glucose uptake early during reperfusion. However, myocardial uptake and phosphorylation of 2-deoxyglucose remains enhanced late during reperfusion, when pre-ischemic distribution of GLUT-4 is almost completely restored, indicating that additional mechanisms are likely to be involved in post-ischemic stimulation of glucose uptake.


Assuntos
Desoxiglucose/metabolismo , Proteínas de Transporte de Monossacarídeos/genética , Proteínas Musculares , Traumatismo por Reperfusão Miocárdica/metabolismo , Miocárdio/metabolismo , Animais , Transporte Biológico Ativo/efeitos dos fármacos , Glucose/metabolismo , Transportador de Glucose Tipo 1 , Transportador de Glucose Tipo 4 , Glicólise , Técnicas In Vitro , Insulina/farmacologia , Cinética , Masculino , Proteínas de Transporte de Monossacarídeos/metabolismo , Traumatismo por Reperfusão Miocárdica/fisiopatologia , Perfusão , Ratos , Sarcolema/metabolismo , Frações Subcelulares/metabolismo , Função Ventricular Esquerda
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