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First published online June 5, 2008
Experimental Biology and Medicine 233:1142-1148 (2008)
doi: 10.3181/0801-RM-33
© 2008 by the Society for Experimental Biology and Medicine

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ORIGINAL RESEARCH ARTICLE

Cardiac Glucose Uptake and Suppressed Expression/Translocation of Myocardium Glucose Transport-4 in Dogs Undergoing Ischemia-Reperfusion

Gui-You Liang1, Qing-Yong Cai, Yi-Ming Niu, Hong Zheng, Zhen-Yu Gao, Da-Xing Liu and Gang Xu

Affiliated Hospital of Zunyi Medical College, Department of Thoracic and Cardiovascular Surgery, Zunyi, Guizhou 563003, China

To whom requests for reprints should be addressed at 1 Affiliated Hospital of Zunyi Medical College, 149 Da-Lian Road, Zunyi, Guizhou 563003, China. E-mail: guiyou515{at}163.com

Impaired glucose metabolism is implicated in cardiac failure during ischemia-reperfusion. This study examined cardiac glucose uptake and expression of glucose transport-4 (GLUT-4) in dogs undergoing ischemia-reperfusion. Cardiac ischemia was induced by cardiopulmonary bypass for 30 min or 120 min in dogs. Plasma insulin and glucose concentrations were measured at pre-bypass (control), and aortic cross-clamp off (ischemia-reperfusion) at 15, 45, and 75 min. At the same time, the left ventricle biopsies were taken for GLUT-4 immunohistochemistry and glycogen content analysis. In dogs receiving 120-min ischemia, coronary arterial and venous glucose concentrations were increased, but the net glucose uptake in ischemia-reperfusion heart were significantly decreased from 25% (control) to zero at 15 and 45 min of reperfusion, and recovered to only 7% after 75 min reperfusion. Myocardium glycogen contents were decreased by 65%. Plasma insulin levels and Insulin Resistant Index were markedly increased in dogs undergoing 120-min ischemia and reperfusion. These changes were relatively mild and reversible in dogs receiving only 30-min ischemia followed by reperfusion. Expression of total GLUT-4 in myocardium was decreased 40% and translocation of GLUT-4 from cytoplasm to surface membrane was decreased 90% in dogs receiving 120-min ischemia followed by 15-min reperfusion. Suppressed translocation of GLUT-4 was also evident in dogs receiving 30-min ischemia, but to a lesser extent. Reduced myocardium glucose uptake, utilization, and glycogen content are clearly associated with ischemia-reperfusion heart injury. This appears to be due, at least in part, to suppressed expression and translocation of myocardium GLUT-4.

Key Words: cardiopulmonary bypass • ischemia-reperfusion • dog • myocardial glucose uptake • insulin resistance • glucose transport-4







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