Montessuit C, Papageorgiou I, Remondino-Müller A, Tardy I, Lerch R
Cardiology, Department of Internal Medicine, University Hospital of Geneva, Switzerland.
J Mol Cell Cardiol. 1998 Feb;30(2):393-403. doi: 10.1006/jmcc.1997.0602.
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.
心肌缺血促使胰岛素敏感性葡萄糖转运体GLUT-4从细胞内膜储存部位转位至肌膜。由于葡萄糖代谢对心脏缺血后恢复至关重要,因此在灌注含0.4 mM棕榈酸酯和8 mM葡萄糖培养基的离体大鼠心脏再灌注期间,测定了[3H]标记的2-脱氧葡萄糖的心肌摄取及GLUT-4的亚细胞定位。心脏经历20分钟无血流缺血,随后再灌注长达60分钟。通过细胞分级分离后进行免疫印迹法测定GLUT-4的亚细胞定位。再灌注15分钟和60分钟后,2-脱氧葡萄糖的摄取量(分别为91±9和96±8 nmol/分钟/克湿重)显著高于对照值(65±1 nmol/分钟/克湿重)。缺血促使GLUT-4转位至肌膜,这在再灌注15分钟后仍持续存在。然而,再灌注60分钟后,GLUT-4的亚细胞分布与对照心脏相似。总之,缺血诱导的GLUT-4转位至肌膜的逆转相当缓慢,这可能在再灌注早期促进葡萄糖摄取。然而,在再灌注后期,当GLUT-4的缺血前分布几乎完全恢复时,2-脱氧葡萄糖的心肌摄取和磷酸化仍保持增强,这表明可能有其他机制参与缺血后葡萄糖摄取的刺激过程。